Salter AIRE Elite User manual
800987 Rev H (Side 1) Printed on 25 March 2021
Salter AIRE
Elite
™
Compressor
Instruction Manual
Part No: 8350-1 / 8352-1 / 8353-1
Thank you for selecting the Salter AIRE
Elite
Compressor. Salter Labs is an innovative, industry-
leading manufacturer of respiratory
care devices. Please contact your local Salter Labs
dealer for information about additional products.
SAVE THESE INSTRUCTIONS.
READ ALL INSTRUCTIONS BEFORE USE.
Contents
Important Safeguards………………………………………… 1
Introduction…………………………………………………….. 2
Product Description…………………………………………… 3
Operation………………………………………………………… 4
Cleaning………………………………………………………….. 5
Storage…………………………………………………………… 6
Maintenance……………………………………………………. 7
Expected Service Life ………………………………………... 8
Troubleshooting……………………………………………….. 9
Specifications………………………………………………….. 10
Accessories……………………………………………………... 11
Appendix A…………………………………………………….. 12
1. Important Safeguards
NOTE, CAUTION, WARNING, AND SYMBOLS:
Important information is highlighted by using the following:
NOTE Indicates information that user should pay special
attention to.
CAUTION Indicates correct operating or maintenance
procedures in order to prevent damage to or destruction of
the equipment or other property.
WARNING Indicates potential danger that requires correct
procedures or practices in order to prevent personal injury
.
Symbols:
O
Off, disconnection from the mains
I
On, connection to the mains
～Alternating Current (AC)
IP2X Protected against solid foreign objects having a
diameter of 12.5 mm and greater. No protection
against vertically falling water drops. Keep dry!
Attention
Class II
Refer to instruction manual/ booklet
“BF” symbol, indicate this product is according to
the degree of protecting against electric shock for
the type BF equipment.
Temperature limitation
Disposal of Electrical & Electronic Equipment
(WEEE): This product should be handed over to an
applicable collection point for the recycling of
electrical and electronic equipment. For more
detailed information about the recycling of this
product, please contact your local city office,
household waste disposal service or the retail
store where you purchased this product.
CAUTION U.S. Federal Law restricts this device to sale by or
on the order of a physician.
WARNING To reduce the risk of burns, electrocution, fire or
injury to persons:
1. Always unplug this product immediately after using.
2. Do not use while bathing, showering, dish washing, or
close to water sources of any kind.
3. Do not place or store product where it can fall or be
pulled into a tub or sink.
4. Do not place in or drop into water or other liquid.
5. Do not reach for a product that has fallen into water.
Unplug immediately.
6. This product should never be left unattended when
plugged in.
7. Close supervision is necessary when this product is used
by, on or near children or invalids. Choking accident may
result from a child swallowing a small part that has
become detached from the device or its accessories.
8. Use this product only for its intended use as described
in this manual. Use this product only under doctor’s
direction. Do not use attachments not recommended
by the manufacturer.
9. Never operate this product if a) it has a damaged cord or
plug, b) it is not working properly, c) it has been dropped
or damaged, d) it has been dropped into water. Return
the product to a specified service center for
examination
and repair.
10. Keep the cord away from heated surfaces.
11. Never block the air openings of this product or allow
objects to fall or be inserted into the air vent openings
or place it on a soft surface such as bed or couch, where
the air openings may be blocked.
12. Never use while sleeping or feeling drowsy.
13. Never drop or insert any object into any opening or
hose.
14. No modification of this equipment is allowed.
15. Do not modify this equipment without authorization of
the manufacturer.
16. If this equipment is modified, appropriate inspection
and testing must be conducted to ensure continued safe
use of the equipment.
17. Do not use in outdoors or operate where aerosol (spray)
products are being used or where oxygen is being
administered in a closed environment such as an
oxygen reservoir.
18. Do not wrap the power cord around the compressor
(main unit).
19. Disconnect the power plug by pulling the plug, not by
pulling on the compressor (main unit), or the cord.
20. If the power cord or plug becomes frayed or otherwise
damaged, do not use.
21. Do not place heavy objects on the power cord, or bend
and pull the cord harder than necessary. These actions
could cause an electric shock or fire.
22. Potential allergic reactions to accessible materials used
in the Compressor Nebulizer equipment. If any signs of
allergic reaction or hypersensitivity happen, stop the
treatment immediately, and notify the doctor or nurse.
23. Potential contact injuries for patients used in the
Compressor Nebulizer equipment. If any contact injuries
happen, stop the treatment, and notify the doctor
or nurse.
24. The device enclosure may overheat, users do not touch
more than 10 seconds.
WARNING EMC Statement
This equipment has been tested and found to comply with
the limits for medical devices to the IEC 60601-1:2014. These
limits are designed to provide reasonable protection against
harmful interference in a typical medical installation. This
equipment generates uses and can radiate radio frequency
energy and, if not installed and used in accordance with the
instructions, may cause harmful interference to other
devices in the vicinity. However, there is no guarantee that
interference will not occur in a particular installation. If this
equipment does cause harmful interference to other
devices, which can be determined by turning the equipment
off and on, the user is encouraged to try to correct the
interference by one or more of the following measures:
Reorient or relocate the receiving device.
Increase the separation between the equipment.
Connect the equipment into an outlet on a circuit
different from that to which the other device(s) are
connected.
Consult the manufacturer or field service technician
for help.
CAUTION If there is a possibility of electro-magnetic
interference with mobile phones, please increase the
distance (3.3m) between devices or turn off the mobile
phone.
2. Introduction
2.1 Intended Use
The Salter AIRE
Elite
Compressor System is intended to
provide a source of compressed air for aerosol therapy. It is
used in conjunction with a jet (pneumatic) nebulizer to
produce medicated aerosols for inhalation by pediatric and
adult patients with respiratory symptoms.
CAUTION Aerosolize liquid medication except Pentamidine
for inhalation by the patients. Indications for therapy
include asthma, chronic bronchitis, infection of the upper
respiratory tract, chronic obstructive pulmonary disease
(COPD) and other respiratory disorders in accordance with a
medical doctor’s prescription. Except the usage mentioned
above, please do not use this product for any other purpose.
This device can be used with adults or pediatric patients
under physician’s prescription.
2.2 Safety Precaution Instruction
When using this electrical product, especially when children
are present, one should always follow basic safety
precautions. Do not install, maintain or operate this
equipment without reading, understanding and following
the proper Salter AIRE
Elite
Compressor System instruction
manual, otherwise injury or damage may result.
For 120V only-
This appliance has a polarized plug (one blade
is wider than the other). To reduce the risk of electric shock,
this plug is intended to fit into a polarized outlet only one
way. If the plug does not fit fully into the outlet, reverse the
plug. If it still does not fit, contact a qualified electrician.
Do not modify the plug in any way.
3. Product Description
1. Power Switch 2. Filter Cap (disposable filter
inside)
3. Air-Outlet Connector 4. Integrated Carrying Handle
5. Power Cord 6. Nebulizer Cup Holder
7. Cooling Air Openings
4. Operation
NOTE Before initial operation, the nebulizer cup assembly
should be cleaned following instructions described in the
“Cleaning” section.
WARNING Before connecting the power cord, make sure the
I/O (ON/OFF) switch is in the O (OFF) position.
The plug is also served to disconnect the device. Do not
position the equipment so that it is difficult to operate
the disconnecting device.
4.1 Daily Use Operation
CAUTION The Salter AIRE Elite Compressor System is
designed for intermittent use only. Do not operate it
continuously for more than 30 minutes for a single use
without turning it off and following a cooling period for least
30 minutes.
1. Before each use inspect the Salter AIRE
Elite
Compressor and nebulizer cup assembly for damage or
wear, replace as needed.
2. Place the Salter AIRE
Elite
Compressor on a table or
other flat stable surface. Be sure you can easily reach
the controls when seated. Do not use this device on the
floor.
3. With the power switch in the O (OFF) position, plug the
power cord into an appropriate electrical wall outlet.
4. Connect one end of the tubing to the compressor air-
800987 Rev H (Side 1) Printed on 25 March 2021
Salter AIRE
Elite
™
Compressor
Instruction Manual
Part No: 8350-1 / 8352-1 / 8353-1
Thank you for selecting the Salter AIRE
Elite
Compressor. Salter Labs is an innovative, industry-
leading manufacturer of respiratory
care devices. Please contact your local Salter Labs
dealer for information about additional products.
SAVE THESE INSTRUCTIONS.
READ ALL INSTRUCTIONS BEFORE USE.
Contents
Important Safeguards………………………………………… 1
Introduction…………………………………………………….. 2
Product Description…………………………………………… 3
Operation………………………………………………………… 4
Cleaning………………………………………………………….. 5
Storage…………………………………………………………… 6
Maintenance……………………………………………………. 7
Expected Service Life ………………………………………... 8
Troubleshooting……………………………………………….. 9
Specifications………………………………………………….. 10
Accessories……………………………………………………... 11
Appendix A…………………………………………………….. 12
1. Important Safeguards
NOTE, CAUTION, WARNING, AND SYMBOLS:
Important information is highlighted by using the following:
NOTE Indicates information that user should pay special
attention to.
CAUTION Indicates correct operating or maintenance
procedures in order to prevent damage to or destruction of
the equipment or other property.
WARNING Indicates potential danger that requires correct
procedures or practices in order to prevent personal injury
.
Symbols:
O
Off, disconnection from the mains
I
On, connection to the mains
～Alternating Current (AC)
IP2X Protected against solid foreign objects having a
diameter of 12.5 mm and greater. No protection
against vertically falling water drops. Keep dry!
Attention
Class II
Refer to instruction manual/ booklet
“BF” symbol, indicate this product is according to
the degree of protecting against electric shock for
the type BF equipment.
Temperature limitation
Disposal of Electrical & Electronic Equipment
(WEEE): This product should be handed over to an
applicable collection point for the recycling of
electrical and electronic equipment. For more
detailed information about the recycling of this
product, please contact your local city office,
household waste disposal service or the retail
store where you purchased this product.
CAUTION U.S. Federal Law restricts this device to sale by or
on the order of a physician.
WARNING To reduce the risk of burns, electrocution, fire or
injury to persons:
1. Always unplug this product immediately after using.
2. Do not use while bathing, showering, dish washing, or
close to water sources of any kind.
3. Do not place or store product where it can fall or be
pulled into a tub or sink.
4. Do not place in or drop into water or other liquid.
5. Do not reach for a product that has fallen into water.
Unplug immediately.
6. This product should never be left unattended when
plugged in.
7. Close supervision is necessary when this product is used
by, on or near children or invalids. Choking accident may
result from a child swallowing a small part that has
become detached from the device or its accessories.
8. Use this product only for its intended use as described
in this manual. Use this product only under doctor’s
direction. Do not use attachments not recommended
by the manufacturer.
9. Never operate this product if a) it has a damaged cord or
plug, b) it is not working properly, c) it has been dropped
or damaged, d) it has been dropped into water. Return
the product to a specified service center for
examination
and repair.
10. Keep the cord away from heated surfaces.
11. Never block the air openings of this product or allow
objects to fall or be inserted into the air vent openings
or place it on a soft surface such as bed or couch, where
the air openings may be blocked.
12. Never use while sleeping or feeling drowsy.
13. Never drop or insert any object into any opening or
hose.
14. No modification of this equipment is allowed.
15. Do not modify this equipment without authorization of
the manufacturer.
16. If this equipment is modified, appropriate inspection
and testing must be conducted to ensure continued safe
use of the equipment.
17. Do not use in outdoors or operate where aerosol (spray)
products are being used or where oxygen is being
administered in a closed environment such as an
oxygen reservoir.
18. Do not wrap the power cord around the compressor
(main unit).
19. Disconnect the power plug by pulling the plug, not by
pulling on the compressor (main unit), or the cord.
20. If the power cord or plug becomes frayed or otherwise
damaged, do not use.
21. Do not place heavy objects on the power cord, or bend
and pull the cord harder than necessary. These actions
could cause an electric shock or fire.
22. Potential allergic reactions to accessible materials used
in the Compressor Nebulizer equipment. If any signs of
allergic reaction or hypersensitivity happen, stop the
treatment immediately, and notify the doctor or nurse.
23. Potential contact injuries for patients used in the
Compressor Nebulizer equipment. If any contact injuries
happen, stop the treatment, and notify the doctor
or nurse.
24. The device enclosure may overheat, users do not touch
more than 10 seconds.
WARNING EMC Statement
This equipment has been tested and found to comply with
the limits for medical devices to the IEC 60601-1:2014. These
limits are designed to provide reasonable protection against
harmful interference in a typical medical installation. This
equipment generates uses and can radiate radio frequency
energy and, if not installed and used in accordance with the
instructions, may cause harmful interference to other
devices in the vicinity. However, there is no guarantee that
interference will not occur in a particular installation. If this
equipment does cause harmful interference to other
devices, which can be determined by turning the equipment
off and on, the user is encouraged to try to correct the
interference by one or more of the following measures:
Reorient or relocate the receiving device.
Increase the separation between the equipment.
Connect the equipment into an outlet on a circuit
different from that to which the other device(s) are
connected.
Consult the manufacturer or field service technician
for help.
CAUTION If there is a possibility of electro-magnetic
interference with mobile phones, please increase the
distance (3.3m) between devices or turn off the mobile
phone.
2. Introduction
2.1 Intended Use
The Salter AIRE
Elite
Compressor System is intended to
provide a source of compressed air for aerosol therapy. It is
used in conjunction with a jet (pneumatic) nebulizer to
produce medicated aerosols for inhalation by pediatric and
adult patients with respiratory symptoms.
CAUTION Aerosolize liquid medication except Pentamidine
for inhalation by the patients. Indications for therapy
include asthma, chronic bronchitis, infection of the upper
respiratory tract, chronic obstructive pulmonary disease
(COPD) and other respiratory disorders in accordance with a
medical doctor’s prescription. Except the usage mentioned
above, please do not use this product for any other purpose.
This device can be used with adults or pediatric patients
under physician’s prescription.
2.2 Safety Precaution Instruction
When using this electrical product, especially when children
are present, one should always follow basic safety
precautions. Do not install, maintain or operate this
equipment without reading, understanding and following
the proper Salter AIRE
Elite
Compressor System instruction
manual, otherwise injury or damage may result.
For 120V only-
This appliance has a polarized plug (one blade
is wider than the other). To reduce the risk of electric shock,
this plug is intended to fit into a polarized outlet only one
way. If the plug does not fit fully into the outlet, reverse the
plug. If it still does not fit, contact a qualified electrician.
Do not modify the plug in any way.
3. Product Description
1. Power Switch 2. Filter Cap (disposable filter
inside)
3. Air-Outlet Connector 4. Integrated Carrying Handle
5. Power Cord 6. Nebulizer Cup Holder
7. Cooling Air Openings
4. Operation
NOTE Before initial operation, the nebulizer cup assembly
should be cleaned following instructions described in the
“Cleaning” section.
WARNING Before connecting the power cord, make sure the
I/O (ON/OFF) switch is in the O (OFF) position.
The plug is also served to disconnect the device. Do not
position the equipment so that it is difficult to operate
the disconnecting device.
4.1 Daily Use Operation
CAUTION The Salter AIRE Elite Compressor System is
designed for intermittent use only. Do not operate it
continuously for more than 30 minutes for a single use
without turning it off and following a cooling period for least
30 minutes.
1. Before each use inspect the Salter AIRE
Elite
Compressor and nebulizer cup assembly for damage or
wear, replace as needed.
2. Place the Salter AIRE
Elite
Compressor on a table or
other flat stable surface. Be sure you can easily reach
the controls when seated. Do not use this device on the
floor.
3. With the power switch in the O (OFF) position, plug the
power cord into an appropriate electrical wall outlet.
4. Connect one end of the tubing to the compressor air-
800987 Rev H (Side 1) Printed on 25 March 2021
Salter AIRE
Elite
™
Compressor
Instruction Manual
Part No: 8350-1 / 8352-1 / 8353-1
Thank you for selecting the Salter AIRE
Elite
Compressor. Salter Labs is an innovative, industry-
leading manufacturer of respiratory
care devices. Please contact your local Salter Labs
dealer for information about additional products.
SAVE THESE INSTRUCTIONS.
READ ALL INSTRUCTIONS BEFORE USE.
Contents
Important Safeguards………………………………………… 1
Introduction…………………………………………………….. 2
Product Description…………………………………………… 3
Operation………………………………………………………… 4
Cleaning………………………………………………………….. 5
Storage…………………………………………………………… 6
Maintenance……………………………………………………. 7
Expected Service Life ………………………………………... 8
Troubleshooting……………………………………………….. 9
Specifications………………………………………………….. 10
Accessories……………………………………………………... 11
Appendix A…………………………………………………….. 12
1. Important Safeguards
NOTE, CAUTION, WARNING, AND SYMBOLS:
Important information is highlighted by using the following:
NOTE Indicates information that user should pay special
attention to.
CAUTION Indicates correct operating or maintenance
procedures in order to prevent damage to or destruction of
the equipment or other property.
WARNING Indicates potential danger that requires correct
procedures or practices in order to prevent personal injury
.
Symbols:
O
Off, disconnection from the mains
I
On, connection to the mains
～Alternating Current (AC)
IP2X Protected against solid foreign objects having a
diameter of 12.5 mm and greater. No protection
against vertically falling water drops. Keep dry!
Attention
Class II
Refer to instruction manual/ booklet
“BF” symbol, indicate this product is according to
the degree of protecting against electric shock for
the type BF equipment.
Temperature limitation
Disposal of Electrical & Electronic Equipment
(WEEE): This product should be handed over to an
applicable collection point for the recycling of
electrical and electronic equipment. For more
detailed information about the recycling of this
product, please contact your local city office,
household waste disposal service or the retail
store where you purchased this product.
CAUTION U.S. Federal Law restricts this device to sale by or
on the order of a physician.
WARNING To reduce the risk of burns, electrocution, fire or
injury to persons:
1. Always unplug this product immediately after using.
2. Do not use while bathing, showering, dish washing, or
close to water sources of any kind.
3. Do not place or store product where it can fall or be
pulled into a tub or sink.
4. Do not place in or drop into water or other liquid.
5. Do not reach for a product that has fallen into water.
Unplug immediately.
6. This product should never be left unattended when
plugged in.
7. Close supervision is necessary when this product is used
by, on or near children or invalids. Choking accident may
result from a child swallowing a small part that has
become detached from the device or its accessories.
8. Use this product only for its intended use as described
in this manual. Use this product only under doctor’s
direction. Do not use attachments not recommended
by the manufacturer.
9. Never operate this product if a) it has a damaged cord or
plug, b) it is not working properly, c) it has been dropped
or damaged, d) it has been dropped into water. Return
the product to a specified service center for
examination
and repair.
10. Keep the cord away from heated surfaces.
11. Never block the air openings of this product or allow
objects to fall or be inserted into the air vent openings
or place it on a soft surface such as bed or couch, where
the air openings may be blocked.
12. Never use while sleeping or feeling drowsy.
13. Never drop or insert any object into any opening or
hose.
14. No modification of this equipment is allowed.
15. Do not modify this equipment without authorization of
the manufacturer.
16. If this equipment is modified, appropriate inspection
and testing must be conducted to ensure continued safe
use of the equipment.
17. Do not use in outdoors or operate where aerosol (spray)
products are being used or where oxygen is being
administered in a closed environment such as an
oxygen reservoir.
18. Do not wrap the power cord around the compressor
(main unit).
19. Disconnect the power plug by pulling the plug, not by
pulling on the compressor (main unit), or the cord.
20. If the power cord or plug becomes frayed or otherwise
damaged, do not use.
21. Do not place heavy objects on the power cord, or bend
and pull the cord harder than necessary. These actions
could cause an electric shock or fire.
22. Potential allergic reactions to accessible materials used
in the Compressor Nebulizer equipment. If any signs of
allergic reaction or hypersensitivity happen, stop the
treatment immediately, and notify the doctor or nurse.
23. Potential contact injuries for patients used in the
Compressor Nebulizer equipment. If any contact injuries
happen, stop the treatment, and notify the doctor
or nurse.
24. The device enclosure may overheat, users do not touch
more than 10 seconds.
WARNING EMC Statement
This equipment has been tested and found to comply with
the limits for medical devices to the IEC 60601-1:2014. These
limits are designed to provide reasonable protection against
harmful interference in a typical medical installation. This
equipment generates uses and can radiate radio frequency
energy and, if not installed and used in accordance with the
instructions, may cause harmful interference to other
devices in the vicinity. However, there is no guarantee that
interference will not occur in a particular installation. If this
equipment does cause harmful interference to other
devices, which can be determined by turning the equipment
off and on, the user is encouraged to try to correct the
interference by one or more of the following measures:
Reorient or relocate the receiving device.
Increase the separation between the equipment.
Connect the equipment into an outlet on a circuit
different from that to which the other device(s) are
connected.
Consult the manufacturer or field service technician
for help.
CAUTION If there is a possibility of electro-magnetic
interference with mobile phones, please increase the
distance (3.3m) between devices or turn off the mobile
phone.
2. Introduction
2.1 Intended Use
The Salter AIRE
Elite
Compressor System is intended to
provide a source of compressed air for aerosol therapy. It is
used in conjunction with a jet (pneumatic) nebulizer to
produce medicated aerosols for inhalation by pediatric and
adult patients with respiratory symptoms.
CAUTION Aerosolize liquid medication except Pentamidine
for inhalation by the patients. Indications for therapy
include asthma, chronic bronchitis, infection of the upper
respiratory tract, chronic obstructive pulmonary disease
(COPD) and other respiratory disorders in accordance with a
medical doctor’s prescription. Except the usage mentioned
above, please do not use this product for any other purpose.
This device can be used with adults or pediatric patients
under physician’s prescription.
2.2 Safety Precaution Instruction
When using this electrical product, especially when children
are present, one should always follow basic safety
precautions. Do not install, maintain or operate this
equipment without reading, understanding and following
the proper Salter AIRE
Elite
Compressor System instruction
manual, otherwise injury or damage may result.
For 120V only-
This appliance has a polarized plug (one blade
is wider than the other). To reduce the risk of electric shock,
this plug is intended to fit into a polarized outlet only one
way. If the plug does not fit fully into the outlet, reverse the
plug. If it still does not fit, contact a qualified electrician.
Do not modify the plug in any way.
3. Product Description
1. Power Switch 2. Filter Cap (disposable filter
inside)
3. Air-Outlet Connector 4. Integrated Carrying Handle
5. Power Cord 6. Nebulizer Cup Holder
7. Cooling Air Openings
4. Operation
NOTE Before initial operation, the nebulizer cup assembly
should be cleaned following instructions described in the
“Cleaning” section.
WARNING Before connecting the power cord, make sure the
I/O (ON/OFF) switch is in the O (OFF) position.
The plug is also served to disconnect the device. Do not
position the equipment so that it is difficult to operate
the disconnecting device.
4.1 Daily Use Operation
CAUTION The Salter AIRE Elite Compressor System is
designed for intermittent use only. Do not operate it
continuously for more than 30 minutes for a single use
without turning it off and following a cooling period for least
30 minutes.
1. Before each use inspect the Salter AIRE
Elite
Compressor and nebulizer cup assembly for damage or
wear, replace as needed.
2. Place the Salter AIRE
Elite
Compressor on a table or
other flat stable surface. Be sure you can easily reach
the controls when seated. Do not use this device on the
floor.
3. With the power switch in the O (OFF) position, plug the
power cord into an appropriate electrical wall outlet.
4. Connect one end of the tubing to the compressor air-
800987 Rev H (Side 1) Printed on 25 March 2021
Salter AIRE
Elite
™
Compressor
Instruction Manual
Part No: 8350-1 / 8352-1 / 8353-1
Thank you for selecting the Salter AIRE
Elite
Compressor. Salter Labs is an innovative, industry-
leading manufacturer of respiratory
care devices. Please contact your local Salter Labs
dealer for information about additional products.
SAVE THESE INSTRUCTIONS.
READ ALL INSTRUCTIONS BEFORE USE.
Contents
Important Safeguards………………………………………… 1
Introduction…………………………………………………….. 2
Product Description…………………………………………… 3
Operation………………………………………………………… 4
Cleaning………………………………………………………….. 5
Storage…………………………………………………………… 6
Maintenance……………………………………………………. 7
Expected Service Life ………………………………………... 8
Troubleshooting……………………………………………….. 9
Specifications………………………………………………….. 10
Accessories……………………………………………………... 11
Appendix A…………………………………………………….. 12
1. Important Safeguards
NOTE, CAUTION, WARNING, AND SYMBOLS:
Important information is highlighted by using the following:
NOTE Indicates information that user should pay special
attention to.
CAUTION Indicates correct operating or maintenance
procedures in order to prevent damage to or destruction of
the equipment or other property.
WARNING Indicates potential danger that requires correct
procedures or practices in order to prevent personal injury
.
Symbols:
O
Off, disconnection from the mains
I
On, connection to the mains
～Alternating Current (AC)
IP2X Protected against solid foreign objects having a
diameter of 12.5 mm and greater. No protection
against vertically falling water drops. Keep dry!
Attention
Class II
Refer to instruction manual/ booklet
“BF” symbol, indicate this product is according to
the degree of protecting against electric shock for
the type BF equipment.
Temperature limitation
Disposal of Electrical & Electronic Equipment
(WEEE): This product should be handed over to an
applicable collection point for the recycling of
electrical and electronic equipment. For more
detailed information about the recycling of this
product, please contact your local city office,
household waste disposal service or the retail
store where you purchased this product.
CAUTION U.S. Federal Law restricts this device to sale by or
on the order of a physician.
WARNING To reduce the risk of burns, electrocution, fire or
injury to persons:
1. Always unplug this product immediately after using.
2. Do not use while bathing, showering, dish washing, or
close to water sources of any kind.
3. Do not place or store product where it can fall or be
pulled into a tub or sink.
4. Do not place in or drop into water or other liquid.
5. Do not reach for a product that has fallen into water.
Unplug immediately.
6. This product should never be left unattended when
plugged in.
7. Close supervision is necessary when this product is used
by, on or near children or invalids. Choking accident may
result from a child swallowing a small part that has
become detached from the device or its accessories.
8. Use this product only for its intended use as described
in this manual. Use this product only under doctor’s
direction. Do not use attachments not recommended
by the manufacturer.
9. Never operate this product if a) it has a damaged cord or
plug, b) it is not working properly, c) it has been dropped
or damaged, d) it has been dropped into water. Return
the product to a specified service center for
examination
and repair.
10. Keep the cord away from heated surfaces.
11. Never block the air openings of this product or allow
objects to fall or be inserted into the air vent openings
or place it on a soft surface such as bed or couch, where
the air openings may be blocked.
12. Never use while sleeping or feeling drowsy.
13. Never drop or insert any object into any opening or
hose.
14. No modification of this equipment is allowed.
15. Do not modify this equipment without authorization of
the manufacturer.
16. If this equipment is modified, appropriate inspection
and testing must be conducted to ensure continued safe
use of the equipment.
17. Do not use in outdoors or operate where aerosol (spray)
products are being used or where oxygen is being
administered in a closed environment such as an
oxygen reservoir.
18. Do not wrap the power cord around the compressor
(main unit).
19. Disconnect the power plug by pulling the plug, not by
pulling on the compressor (main unit), or the cord.
20. If the power cord or plug becomes frayed or otherwise
damaged, do not use.
21. Do not place heavy objects on the power cord, or bend
and pull the cord harder than necessary. These actions
could cause an electric shock or fire.
22. Potential allergic reactions to accessible materials used
in the Compressor Nebulizer equipment. If any signs of
allergic reaction or hypersensitivity happen, stop the
treatment immediately, and notify the doctor or nurse.
23. Potential contact injuries for patients used in the
Compressor Nebulizer equipment. If any contact injuries
happen, stop the treatment, and notify the doctor
or nurse.
24. The device enclosure may overheat, users do not touch
more than 10 seconds.
WARNING EMC Statement
This equipment has been tested and found to comply with
the limits for medical devices to the IEC 60601-1:2014. These
limits are designed to provide reasonable protection against
harmful interference in a typical medical installation. This
equipment generates uses and can radiate radio frequency
energy and, if not installed and used in accordance with the
instructions, may cause harmful interference to other
devices in the vicinity. However, there is no guarantee that
interference will not occur in a particular installation. If this
equipment does cause harmful interference to other
devices, which can be determined by turning the equipment
off and on, the user is encouraged to try to correct the
interference by one or more of the following measures:
Reorient or relocate the receiving device.
Increase the separation between the equipment.
Connect the equipment into an outlet on a circuit
different from that to which the other device(s) are
connected.
Consult the manufacturer or field service technician
for help.
CAUTION If there is a possibility of electro-magnetic
interference with mobile phones, please increase the
distance (3.3m) between devices or turn off the mobile
phone.
2. Introduction
2.1 Intended Use
The Salter AIRE
Elite
Compressor System is intended to
provide a source of compressed air for aerosol therapy. It is
used in conjunction with a jet (pneumatic) nebulizer to
produce medicated aerosols for inhalation by pediatric and
adult patients with respiratory symptoms.
CAUTION Aerosolize liquid medication except Pentamidine
for inhalation by the patients. Indications for therapy
include asthma, chronic bronchitis, infection of the upper
respiratory tract, chronic obstructive pulmonary disease
(COPD) and other respiratory disorders in accordance with a
medical doctor’s prescription. Except the usage mentioned
above, please do not use this product for any other purpose.
This device can be used with adults or pediatric patients
under physician’s prescription.
2.2 Safety Precaution Instruction
When using this electrical product, especially when children
are present, one should always follow basic safety
precautions. Do not install, maintain or operate this
equipment without reading, understanding and following
the proper Salter AIRE
Elite
Compressor System instruction
manual, otherwise injury or damage may result.
For 120V only-
This appliance has a polarized plug (one blade
is wider than the other). To reduce the risk of electric shock,
this plug is intended to fit into a polarized outlet only one
way. If the plug does not fit fully into the outlet, reverse the
plug. If it still does not fit, contact a qualified electrician.
Do not modify the plug in any way.
3. Product Description
1. Power Switch 2. Filter Cap (disposable filter
inside)
3. Air-Outlet Connector 4. Integrated Carrying Handle
5. Power Cord 6. Nebulizer Cup Holder
7. Cooling Air Openings
4. Operation
NOTE Before initial operation, the nebulizer cup assembly
should be cleaned following instructions described in the
“Cleaning” section.
WARNING Before connecting the power cord, make sure the
I/O (ON/OFF) switch is in the O (OFF) position.
The plug is also served to disconnect the device. Do not
position the equipment so that it is difficult to operate
the disconnecting device.
4.1 Daily Use Operation
CAUTION The Salter AIRE Elite Compressor System is
designed for intermittent use only. Do not operate it
continuously for more than 30 minutes for a single use
without turning it off and following a cooling period for least
30 minutes.
1. Before each use inspect the Salter AIRE
Elite
Compressor and nebulizer cup assembly for damage or
wear, replace as needed.
2. Place the Salter AIRE
Elite
Compressor on a table or
other flat stable surface. Be sure you can easily reach
the controls when seated. Do not use this device on the
floor.
3. With the power switch in the O (OFF) position, plug the
power cord into an appropriate electrical wall outlet.
4. Connect one end of the tubing to the compressor air-
800987 Rev H (Side 1) Printed on 25 March 2021
Salter AIRE
Elite
™
Compressor
Instruction Manual
Part No: 8350-1 / 8352-1 / 8353-1
Thank you for selecting the Salter AIRE
Elite
Compressor. Salter Labs is an innovative, industry-
leading manufacturer of respiratory
care devices. Please contact your local Salter Labs
dealer for information about additional products.
SAVE THESE INSTRUCTIONS.
READ ALL INSTRUCTIONS BEFORE USE.
Contents
Important Safeguards………………………………………… 1
Introduction…………………………………………………….. 2
Product Description…………………………………………… 3
Operation………………………………………………………… 4
Cleaning………………………………………………………….. 5
Storage…………………………………………………………… 6
Maintenance……………………………………………………. 7
Expected Service Life ………………………………………... 8
Troubleshooting……………………………………………….. 9
Specifications………………………………………………….. 10
Accessories……………………………………………………... 11
Appendix A…………………………………………………….. 12
1. Important Safeguards
NOTE, CAUTION, WARNING, AND SYMBOLS:
Important information is highlighted by using the following:
NOTE Indicates information that user should pay special
attention to.
CAUTION Indicates correct operating or maintenance
procedures in order to prevent damage to or destruction of
the equipment or other property.
WARNING Indicates potential danger that requires correct
procedures or practices in order to prevent personal injury
.
Symbols:
O
Off, disconnection from the mains
I
On, connection to the mains
～Alternating Current (AC)
IP2X Protected against solid foreign objects having a
diameter of 12.5 mm and greater. No protection
against vertically falling water drops. Keep dry!
Attention
Class II
Refer to instruction manual/ booklet
“BF” symbol, indicate this product is according to
the degree of protecting against electric shock for
the type BF equipment.
Temperature limitation
Disposal of Electrical & Electronic Equipment
(WEEE): This product should be handed over to an
applicable collection point for the recycling of
electrical and electronic equipment. For more
detailed information about the recycling of this
product, please contact your local city office,
household waste disposal service or the retail
store where you purchased this product.
CAUTION U.S. Federal Law restricts this device to sale by or
on the order of a physician.
WARNING To reduce the risk of burns, electrocution, fire or
injury to persons:
1. Always unplug this product immediately after using.
2. Do not use while bathing, showering, dish washing, or
close to water sources of any kind.
3. Do not place or store product where it can fall or be
pulled into a tub or sink.
4. Do not place in or drop into water or other liquid.
5. Do not reach for a product that has fallen into water.
Unplug immediately.
6. This product should never be left unattended when
plugged in.
7. Close supervision is necessary when this product is used
by, on or near children or invalids. Choking accident may
result from a child swallowing a small part that has
become detached from the device or its accessories.
8. Use this product only for its intended use as described
in this manual. Use this product only under doctor’s
direction. Do not use attachments not recommended
by the manufacturer.
9. Never operate this product if a) it has a damaged cord or
plug, b) it is not working properly, c) it has been dropped
or damaged, d) it has been dropped into water. Return
the product to a specified service center for
examination
and repair.
10. Keep the cord away from heated surfaces.
11. Never block the air openings of this product or allow
objects to fall or be inserted into the air vent openings
or place it on a soft surface such as bed or couch, where
the air openings may be blocked.
12. Never use while sleeping or feeling drowsy.
13. Never drop or insert any object into any opening or
hose.
14. No modification of this equipment is allowed.
15. Do not modify this equipment without authorization of
the manufacturer.
16. If this equipment is modified, appropriate inspection
and testing must be conducted to ensure continued safe
use of the equipment.
17. Do not use in outdoors or operate where aerosol (spray)
products are being used or where oxygen is being
administered in a closed environment such as an
oxygen reservoir.
18. Do not wrap the power cord around the compressor
(main unit).
19. Disconnect the power plug by pulling the plug, not by
pulling on the compressor (main unit), or the cord.
20. If the power cord or plug becomes frayed or otherwise
damaged, do not use.
21. Do not place heavy objects on the power cord, or bend
and pull the cord harder than necessary. These actions
could cause an electric shock or fire.
22. Potential allergic reactions to accessible materials used
in the Compressor Nebulizer equipment. If any signs of
allergic reaction or hypersensitivity happen, stop the
treatment immediately, and notify the doctor or nurse.
23. Potential contact injuries for patients used in the
Compressor Nebulizer equipment. If any contact injuries
happen, stop the treatment, and notify the doctor
or nurse.
24. The device enclosure may overheat, users do not touch
more than 10 seconds.
WARNING EMC Statement
This equipment has been tested and found to comply with
the limits for medical devices to the IEC 60601-1:2014. These
limits are designed to provide reasonable protection against
harmful interference in a typical medical installation. This
equipment generates uses and can radiate radio frequency
energy and, if not installed and used in accordance with the
instructions, may cause harmful interference to other
devices in the vicinity. However, there is no guarantee that
interference will not occur in a particular installation. If this
equipment does cause harmful interference to other
devices, which can be determined by turning the equipment
off and on, the user is encouraged to try to correct the
interference by one or more of the following measures:
Reorient or relocate the receiving device.
Increase the separation between the equipment.
Connect the equipment into an outlet on a circuit
different from that to which the other device(s) are
connected.
Consult the manufacturer or field service technician
for help.
CAUTION If there is a possibility of electro-magnetic
interference with mobile phones, please increase the
distance (3.3m) between devices or turn off the mobile
phone.
2. Introduction
2.1 Intended Use
The Salter AIRE
Elite
Compressor System is intended to
provide a source of compressed air for aerosol therapy. It is
used in conjunction with a jet (pneumatic) nebulizer to
produce medicated aerosols for inhalation by pediatric and
adult patients with respiratory symptoms.
CAUTION Aerosolize liquid medication except Pentamidine
for inhalation by the patients. Indications for therapy
include asthma, chronic bronchitis, infection of the upper
respiratory tract, chronic obstructive pulmonary disease
(COPD) and other respiratory disorders in accordance with a
medical doctor’s prescription. Except the usage mentioned
above, please do not use this product for any other purpose.
This device can be used with adults or pediatric patients
under physician’s prescription.
2.2 Safety Precaution Instruction
When using this electrical product, especially when children
are present, one should always follow basic safety
precautions. Do not install, maintain or operate this
equipment without reading, understanding and following
the proper Salter AIRE
Elite
Compressor System instruction
manual, otherwise injury or damage may result.
For 120V only-
This appliance has a polarized plug (one blade
is wider than the other). To reduce the risk of electric shock,
this plug is intended to fit into a polarized outlet only one
way. If the plug does not fit fully into the outlet, reverse the
plug. If it still does not fit, contact a qualified electrician.
Do not modify the plug in any way.
3. Product Description
1. Power Switch 2. Filter Cap (disposable filter
inside)
3. Air-Outlet Connector 4. Integrated Carrying Handle
5. Power Cord 6. Nebulizer Cup Holder
7. Cooling Air Openings
4. Operation
NOTE Before initial operation, the nebulizer cup assembly
should be cleaned following instructions described in the
“Cleaning” section.
WARNING Before connecting the power cord, make sure the
I/O (ON/OFF) switch is in the O (OFF) position.
The plug is also served to disconnect the device. Do not
position the equipment so that it is difficult to operate
the disconnecting device.
4.1 Daily Use Operation
CAUTION The Salter AIRE Elite Compressor System is
designed for intermittent use only. Do not operate it
continuously for more than 30 minutes for a single use
without turning it off and following a cooling period for least
30 minutes.
1. Before each use inspect the Salter AIRE
Elite
Compressor and nebulizer cup assembly for damage or
wear, replace as needed.
2. Place the Salter AIRE
Elite
Compressor on a table or
other flat stable surface. Be sure you can easily reach
the controls when seated. Do not use this device on the
floor.
3. With the power switch in the O (OFF) position, plug the
power cord into an appropriate electrical wall outlet.
4. Connect one end of the tubing to the compressor air-
800987 Rev H (Side 2) 666001-6720 V1.5
outlet connector.
5. Assemble the nebulizer cup and add indicated
medication to the nebulizer’s cup before use.
6. Attach the other end of the tubing into the air-inlet
connector founded at the bottom of the nebulizer cup.
7. Turn on the Salter AIRE
Elite
Compressor by
pressing the power switch to the I (ON) position
and begin treatment.
8. If treatment needs to be interrupted, simply press
power switch to O (OFF) position.
9. When the treatment is complete, turn off the
compressor by pressing the power switch to O (OFF)
position and unplug the unit from the electrical outlet.
Equipment is not suitable for use in the presence
of a flammable anesthetic mixture with air or with
oxygen or nitrous oxide. This device has no AP or APG
protection.
CAUTION During the treatment, the patient should not
touch the outer case due to expected rise in unit
temperature.
4.2 Safety Overload
NOTE Do not exceed 30 minutes of continuous operation.
1. The motor of this device has a built-in thermal overload
protector. Should the motor overheat, the protector will
automatically shut off the motor. Should this occur, turn
the I/O (ON/OFF) switch to the O (OFF) position and
allow the motor to cool down for approximately 30
minutes before turn it on again.
2. If the overload protector shuts off the motor frequently,
you may have an unstable voltage situation.
3. If the unit shuts down and cannot restart, it may need
to be replaced. Call your provider immediately.
5. Cleaning
5.1 Compressor Outer Case Cleaning
WARNING Electric shock hazard. Do not remove outer case
of this unit. All disassembly and maintenance of this unit
must be done by a qualified service technician. Refer
servicing to qualified service personnel.
WARNING This unit does not require oil. Do not attempt to
lubricate any internal parts.
WARNING Unplug unit before cleaning. Do not submerge in
water for cleaning.
1. Wipe the main unit with a damp cloth every few days to
keep it dust-free.
2. Do not use any powdered type cleaners or soap. Do not
submerge the unit into water.
5.2. Nebulizer Cup Cleaning
Clean the nebulizer after each use. Refer to the cleaning
instructions supplied with your nebulizer
WARNING To prevent possible risk of infection from
contaminated medication, cleaning of the nebulizer is
recommended after each treatment.
NOTE The nebulizer kit is for single patient use only.
NOTE Please follow national requirements to dispose the
unit properly.
6. Storage
Keep the unit and accessories dry. Avoid direct sunshine.
See specifications in Section 10 for appropriate
environmental storage conditions.
7. Maintenance
7.1 General Information
1. This unit is oil-less. Do Not Lubricate.
2. Risk of electric shock. Do not disassemble the main unit.
7.2 Filter Change
NOTE Inspect the filter once every month
and replace as necessary or when filter
turns gray. Please follow the below
instructions as right figures.
1. Open the filter cap.
2. Inspect the filter and if dirty, remove
filter with a small, pointed object.
Discard the filter.
3. Replace with a clean filter. Additional
filters should be purchased from your
provider.
4. Put the filter cap back.
CAUTION Do not use cotton or any other material as a filter.
Do not wash or reuse the filter. Do not operate the unit
without
a filter.
7.3 Service
Except for the above instructed user maintenance, all device
servicing must be performed by a Salter Labs®authorized
service representative. There are no serviceable parts inside
the unit. Contact your Salter Labs dealer or authorized
service center if your unit needs repair.
WARNING Do not tamper with or attempt to repair the
device. Refer servicing to qualified service personnel.
8. Expected Service Life
The products are intended to offer safe and reliable
operation when used or installed according to the
instructions provided by Salter Labs. Salter Labs
recommends that the system be inspected and serviced by
authorized technicians if there are any signs of wear or
concerns with device function and indication on products.
Otherwise, service and inspection of the devices generally
should not be required.
9. Troubleshooting
If your Salter AIRE
Elite
Compressor fails to function,
consult the Troubleshooting guide below. If the problem
persists, consult your equipment provider.
Problem Cause and Solution
Device doesn’t
operate
•Check if plug is properly fit into an
appropriate electrical outlet.
•When device has been run continuously for
over 30 minutes right before using, an auto
shut down may activate by built-in thermal
protector, cool down device for 30 minutes
before next usage.
Weak
Nebulization
•Check for proper electrical voltage.
•Check tubing for blockage or air leakage at
connection to Salter AIRE
Elite
Compressor
or nebulizer cup, replace
as needed.
•Check the nebulizer cup if it is properly
assembled and not damaged. If there is any
damage, replace as needed.
•Check if filter is too dirty, replace
as needed.
10. Specifications
(All specifications are subject to change without notice.)
Electrical Rating
(Note: Refer to the rating
label on the product)
120VAC,60Hz,1.2A
(For 120V System)
230VAC, 50Hz,
0.6A (For 230V
System)
Maximum Compressor
Pressure
≧30 psi
Nebulizer Flow Rate
≧
5.5 lpm
≧
5.0 lpm
Classification
Class II.
BF equipment.
IP2X
No AP/APG protection.
Applied part
Mouthpiece or Nasal mask
Dimensions (W x D x H)
14.6 × 20.3 × 9.5 cm /
5.7” × 7.9” × 3.7”
Weight (approx.)
1.8 kg / 4.0 lb
Fuse (non-user serviceable)
F5AL 250V
T1.6AL 250V
Expected Service Life
3 Years (minimum)
Warranty
5 Years
Environment
Temperature
Operation: 10
℃
to 40
℃
/ 50
℉
to 104
℉
Storage: -15
℃
to 50
℃
/ 5
℉
to 122
℉
Transport: -15
℃
to 70
℃
/ 5
℉
to 158
℉
Humidity
Operation: 10% to 90%RH
non-condensing
Storage: 10% to 90%RH
non-condensing
Transport: 10% to 90% RH
non-condensing
Atmospheric
Pressure
Operation: 700-1060 hPa
11. Accessories
Model Description
8501-1-2 Salter AIRE Elite Replacement filters
8258-0-1 Compressor Carrying bag
8660 NebuTech® Nebulizer – Reusable
8960 NebuTech Nebulizer – Disposable
8967 NebuTech Nebulizer with Pediatric Mask
8984 NebuTech Nebulizer with Adult Mask
8900 Nebulizer with Tee Adapter
8906 Nebulizer with Pediatric Mask
8924 Nebulizer with Adult Mask
12. Appendix A: EMC Information
Guidance and Manufacturer’s Declaration-
Electromagnetic Emissions:
This device is intended for use in the electromagnetic
environment specified below. The user of this device
should make sure it is used in such an environment.
Emissions
Test Compliance Electromagnetic Environment-
Guidance
RF emissions
CISPR 11
Group 1
The device uses RF energy only for its
internal function. Therefore, its RF
emissions are very low and are not
likely to cause any interference in
nearby electronic equipment
RF emissions
CISPR 11
Class B
The device is suitable for use in all
establishments, including domestic
establishments and those directly
connected to the public low-voltage
power supply network.
Harmonic
emissions
IEC61000-3-2
Class A
Voltage
fluctuations
/ Flicker
emissions
IEC61000-3-3
Complies
Warning:
1. The device should not be used adjacent to or stacked with other
equipment.
If adjacent or stacked use is necessary, the device should be
observed to verify normal operation in the configuration in which it
will be used.
2. Use of accessories, transducers and cables other than those
specified or provided by the manufacturer of this equipment could
result in increased electromagnetic emissions or decreased
electromagnetic immunity of this equipment and result in
improper operation.
3. Portable RF communications equipment (including peripherals
such as antenna cables and external antennas) should be used no
closer than 30 cm (12 inches)
to any part of the
Compressor, including cables specified by the
manufacturer. Otherwise, degradation of the performance of this
equipment could result.
Guidance and Manufacturer’s Declaration-
Electromagnetic Immunity:
This device is intended for use in the electromagnetic
environment specified below. The user of this device
should make sure it is used in such an environment.
Immunity Test
IEC60601
test level Compliance Electromagnetic
Environment-Guidance
Electrostatic
Discharge
(ESD)
IEC61000-4-2
±8kV contact
±15kV air
±8kV
contact
±15kV air
Floors should be
wood, concrete or
ceramic tile. If floors
are covered with
synthetic material,
800987 Rev H (Side 2) 666001-6720 V1.5
outlet connector.
5. Assemble the nebulizer cup and add indicated
medication to the nebulizer’s cup before use.
6. Attach the other end of the tubing into the air-inlet
connector founded at the bottom of the nebulizer cup.
7. Turn on the Salter AIRE
Elite
Compressor by
pressing the power switch to the I (ON) position
and begin treatment.
8. If treatment needs to be interrupted, simply press
power switch to O (OFF) position.
9. When the treatment is complete, turn off the
compressor by pressing the power switch to O (OFF)
position and unplug the unit from the electrical outlet.
Equipment is not suitable for use in the presence
of a flammable anesthetic mixture with air or with
oxygen or nitrous oxide. This device has no AP or APG
protection.
CAUTION During the treatment, the patient should not
touch the outer case due to expected rise in unit
temperature.
4.2 Safety Overload
NOTE Do not exceed 30 minutes of continuous operation.
1. The motor of this device has a built-in thermal overload
protector. Should the motor overheat, the protector will
automatically shut off the motor. Should this occur, turn
the I/O (ON/OFF) switch to the O (OFF) position and
allow the motor to cool down for approximately 30
minutes before turn it on again.
2. If the overload protector shuts off the motor frequently,
you may have an unstable voltage situation.
3. If the unit shuts down and cannot restart, it may need
to be replaced. Call your provider immediately.
5. Cleaning
5.1 Compressor Outer Case Cleaning
WARNING Electric shock hazard. Do not remove outer case
of this unit. All disassembly and maintenance of this unit
must be done by a qualified service technician. Refer
servicing to qualified service personnel.
WARNING This unit does not require oil. Do not attempt to
lubricate any internal parts.
WARNING Unplug unit before cleaning. Do not submerge in
water for cleaning.
1. Wipe the main unit with a damp cloth every few days to
keep it dust-free.
2. Do not use any powdered type cleaners or soap. Do not
submerge the unit into water.
5.2. Nebulizer Cup Cleaning
Clean the nebulizer after each use. Refer to the cleaning
instructions supplied with your nebulizer
WARNING To prevent possible risk of infection from
contaminated medication, cleaning of the nebulizer is
recommended after each treatment.
NOTE The nebulizer kit is for single patient use only.
NOTE Please follow national requirements to dispose the
unit properly.
6. Storage
Keep the unit and accessories dry. Avoid direct sunshine.
See specifications in Section 10 for appropriate
environmental storage conditions.
7. Maintenance
7.1 General Information
1. This unit is oil-less. Do Not Lubricate.
2. Risk of electric shock. Do not disassemble the main unit.
7.2 Filter Change
NOTE Inspect the filter once every month
and replace as necessary or when filter
turns gray. Please follow the below
instructions as right figures.
1. Open the filter cap.
2. Inspect the filter and if dirty, remove
filter with a small, pointed object.
Discard the filter.
3. Replace with a clean filter. Additional
filters should be purchased from your
provider.
4. Put the filter cap back.
CAUTION Do not use cotton or any other material as a filter.
Do not wash or reuse the filter. Do not operate the unit
without
a filter.
7.3 Service
Except for the above instructed user maintenance, all device
servicing must be performed by a Salter Labs®authorized
service representative. There are no serviceable parts inside
the unit. Contact your Salter Labs dealer or authorized
service center if your unit needs repair.
WARNING Do not tamper with or attempt to repair the
device. Refer servicing to qualified service personnel.
8. Expected Service Life
The products are intended to offer safe and reliable
operation when used or installed according to the
instructions provided by Salter Labs. Salter Labs
recommends that the system be inspected and serviced by
authorized technicians if there are any signs of wear or
concerns with device function and indication on products.
Otherwise, service and inspection of the devices generally
should not be required.
9. Troubleshooting
If your Salter AIRE
Elite
Compressor fails to function,
consult the Troubleshooting guide below. If the problem
persists, consult your equipment provider.
Problem Cause and Solution
Device doesn’t
operate
•Check if plug is properly fit into an
appropriate electrical outlet.
•When device has been run continuously for
over 30 minutes right before using, an auto
shut down may activate by built-in thermal
protector, cool down device for 30 minutes
before next usage.
Weak
Nebulization
•Check for proper electrical voltage.
•Check tubing for blockage or air leakage at
connection to Salter AIRE
Elite
Compressor
or nebulizer cup, replace
as needed.
•Check the nebulizer cup if it is properly
assembled and not damaged. If there is any
damage, replace as needed.
•Check if filter is too dirty, replace
as needed.
10. Specifications
(All specifications are subject to change without notice.)
Electrical Rating
(Note: Refer to the rating
label on the product)
120VAC,60Hz,1.2A
(For 120V System)
230VAC, 50Hz,
0.6A (For 230V
System)
Maximum Compressor
Pressure
≧30 psi
Nebulizer Flow Rate
≧
5.5 lpm
≧
5.0 lpm
Classification
Class II.
BF equipment.
IP2X
No AP/APG protection.
Applied part
Mouthpiece or Nasal mask
Dimensions (W x D x H)
14.6 × 20.3 × 9.5 cm /
5.7” × 7.9” × 3.7”
Weight (approx.)
1.8 kg / 4.0 lb
Fuse (non-user serviceable)
F5AL 250V
T1.6AL 250V
Expected Service Life
3 Years (minimum)
Warranty
5 Years
Environment
Temperature
Operation: 10
℃
to 40
℃
/ 50
℉
to 104
℉
Storage: -15
℃
to 50
℃
/ 5
℉
to 122
℉
Transport: -15
℃
to 70
℃
/ 5
℉
to 158
℉
Humidity
Operation: 10% to 90%RH
non-condensing
Storage: 10% to 90%RH
non-condensing
Transport: 10% to 90% RH
non-condensing
Atmospheric
Pressure
Operation: 700-1060 hPa
11. Accessories
Model Description
8501-1-2 Salter AIRE Elite Replacement filters
8258-0-1 Compressor Carrying bag
8660 NebuTech® Nebulizer – Reusable
8960 NebuTech Nebulizer – Disposable
8967 NebuTech Nebulizer with Pediatric Mask
8984 NebuTech Nebulizer with Adult Mask
8900 Nebulizer with Tee Adapter
8906 Nebulizer with Pediatric Mask
8924 Nebulizer with Adult Mask
12. Appendix A: EMC Information
Guidance and Manufacturer’s Declaration-
Electromagnetic Emissions:
This device is intended for use in the electromagnetic
environment specified below. The user of this device
should make sure it is used in such an environment.
Emissions
Test Compliance Electromagnetic Environment-
Guidance
RF emissions
CISPR 11
Group 1
The device uses RF energy only for its
internal function. Therefore, its RF
emissions are very low and are not
likely to cause any interference in
nearby electronic equipment
RF emissions
CISPR 11
Class B
The device is suitable for use in all
establishments, including domestic
establishments and those directly
connected to the public low-voltage
power supply network.
Harmonic
emissions
IEC61000-3-2
Class A
Voltage
fluctuations
/ Flicker
emissions
IEC61000-3-3
Complies
Warning:
1. The device should not be used adjacent to or stacked with other
equipment.
If adjacent or stacked use is necessary, the device should be
observed to verify normal operation in the configuration in which it
will be used.
2. Use of accessories, transducers and cables other than those
specified or provided by the manufacturer of this equipment could
result in increased electromagnetic emissions or decreased
electromagnetic immunity of this equipment and result in
improper operation.
3. Portable RF communications equipment (including peripherals
such as antenna cables and external antennas) should be used no
closer than 30 cm (12 inches)
to any part of the
Compressor, including cables specified by the
manufacturer. Otherwise, degradation of the performance of this
equipment could result.
Guidance and Manufacturer’s Declaration-
Electromagnetic Immunity:
This device is intended for use in the electromagnetic
environment specified below. The user of this device
should make sure it is used in such an environment.
Immunity Test
IEC60601
test level Compliance Electromagnetic
Environment-Guidance
Electrostatic
Discharge
(ESD)
IEC61000-4-2
±8kV contact
±15kV air
±8kV
contact
±15kV air
Floors should be
wood, concrete or
ceramic tile. If floors
are covered with
synthetic material,
800987 Rev H (Side 2) 666001-6720 V1.5
outlet connector.
5. Assemble the nebulizer cup and add indicated
medication to the nebulizer’s cup before use.
6. Attach the other end of the tubing into the air-inlet
connector founded at the bottom of the nebulizer cup.
7. Turn on the Salter AIRE
Elite
Compressor by
pressing the power switch to the I (ON) position
and begin treatment.
8. If treatment needs to be interrupted, simply press
power switch to O (OFF) position.
9. When the treatment is complete, turn off the
compressor by pressing the power switch to O (OFF)
position and unplug the unit from the electrical outlet.
Equipment is not suitable for use in the presence
of a flammable anesthetic mixture with air or with
oxygen or nitrous oxide. This device has no AP or APG
protection.
CAUTION During the treatment, the patient should not
touch the outer case due to expected rise in unit
temperature.
4.2 Safety Overload
NOTE Do not exceed 30 minutes of continuous operation.
1. The motor of this device has a built-in thermal overload
protector. Should the motor overheat, the protector will
automatically shut off the motor. Should this occur, turn
the I/O (ON/OFF) switch to the O (OFF) position and
allow the motor to cool down for approximately 30
minutes before turn it on again.
2. If the overload protector shuts off the motor frequently,
you may have an unstable voltage situation.
3. If the unit shuts down and cannot restart, it may need
to be replaced. Call your provider immediately.
5. Cleaning
5.1 Compressor Outer Case Cleaning
WARNING Electric shock hazard. Do not remove outer case
of this unit. All disassembly and maintenance of this unit
must be done by a qualified service technician. Refer
servicing to qualified service personnel.
WARNING This unit does not require oil. Do not attempt to
lubricate any internal parts.
WARNING Unplug unit before cleaning. Do not submerge in
water for cleaning.
1. Wipe the main unit with a damp cloth every few days to
keep it dust-free.
2. Do not use any powdered type cleaners or soap. Do not
submerge the unit into water.
5.2. Nebulizer Cup Cleaning
Clean the nebulizer after each use. Refer to the cleaning
instructions supplied with your nebulizer
WARNING To prevent possible risk of infection from
contaminated medication, cleaning of the nebulizer is
recommended after each treatment.
NOTE The nebulizer kit is for single patient use only.
NOTE Please follow national requirements to dispose the
unit properly.
6. Storage
Keep the unit and accessories dry. Avoid direct sunshine.
See specifications in Section 10 for appropriate
environmental storage conditions.
7. Maintenance
7.1 General Information
1. This unit is oil-less. Do Not Lubricate.
2. Risk of electric shock. Do not disassemble the main unit.
7.2 Filter Change
NOTE Inspect the filter once every month
and replace as necessary or when filter
turns gray. Please follow the below
instructions as right figures.
1. Open the filter cap.
2. Inspect the filter and if dirty, remove
filter with a small, pointed object.
Discard the filter.
3. Replace with a clean filter. Additional
filters should be purchased from your
provider.
4. Put the filter cap back.
CAUTION Do not use cotton or any other material as a filter.
Do not wash or reuse the filter. Do not operate the unit
without
a filter.
7.3 Service
Except for the above instructed user maintenance, all device
servicing must be performed by a Salter Labs®authorized
service representative. There are no serviceable parts inside
the unit. Contact your Salter Labs dealer or authorized
service center if your unit needs repair.
WARNING Do not tamper with or attempt to repair the
device. Refer servicing to qualified service personnel.
8. Expected Service Life
The products are intended to offer safe and reliable
operation when used or installed according to the
instructions provided by Salter Labs. Salter Labs
recommends that the system be inspected and serviced by
authorized technicians if there are any signs of wear or
concerns with device function and indication on products.
Otherwise, service and inspection of the devices generally
should not be required.
9. Troubleshooting
If your Salter AIRE
Elite
Compressor fails to function,
consult the Troubleshooting guide below. If the problem
persists, consult your equipment provider.
Problem Cause and Solution
Device doesn’t
operate
•Check if plug is properly fit into an
appropriate electrical outlet.
•When device has been run continuously for
over 30 minutes right before using, an auto
shut down may activate by built-in thermal
protector, cool down device for 30 minutes
before next usage.
Weak
Nebulization
•Check for proper electrical voltage.
•Check tubing for blockage or air leakage at
connection to Salter AIRE
Elite
Compressor
or nebulizer cup, replace
as needed.
•Check the nebulizer cup if it is properly
assembled and not damaged. If there is any
damage, replace as needed.
•Check if filter is too dirty, replace
as needed.
10. Specifications
(All specifications are subject to change without notice.)
Electrical Rating
(Note: Refer to the rating
label on the product)
120VAC,60Hz,1.2A
(For 120V System)
230VAC, 50Hz,
0.6A (For 230V
System)
Maximum Compressor
Pressure
≧30 psi
Nebulizer Flow Rate
≧
5.5 lpm
≧
5.0 lpm
Classification
Class II.
BF equipment.
IP2X
No AP/APG protection.
Applied part
Mouthpiece or Nasal mask
Dimensions (W x D x H)
14.6 × 20.3 × 9.5 cm /
5.7” × 7.9” × 3.7”
Weight (approx.)
1.8 kg / 4.0 lb
Fuse (non-user serviceable)
F5AL 250V
T1.6AL 250V
Expected Service Life
3 Years (minimum)
Warranty
5 Years
Environment
Temperature
Operation: 10
℃
to 40
℃
/ 50
℉
to 104
℉
Storage: -15
℃
to 50
℃
/ 5
℉
to 122
℉
Transport: -15
℃
to 70
℃
/ 5
℉
to 158
℉
Humidity
Operation: 10% to 90%RH
non-condensing
Storage: 10% to 90%RH
non-condensing
Transport: 10% to 90% RH
non-condensing
Atmospheric
Pressure
Operation: 700-1060 hPa
11. Accessories
Model Description
8501-1-2 Salter AIRE Elite Replacement filters
8258-0-1 Compressor Carrying bag
8660 NebuTech® Nebulizer – Reusable
8960 NebuTech Nebulizer – Disposable
8967 NebuTech Nebulizer with Pediatric Mask
8984 NebuTech Nebulizer with Adult Mask
8900 Nebulizer with Tee Adapter
8906 Nebulizer with Pediatric Mask
8924 Nebulizer with Adult Mask
12. Appendix A: EMC Information
Guidance and Manufacturer’s Declaration-
Electromagnetic Emissions:
This device is intended for use in the electromagnetic
environment specified below. The user of this device
should make sure it is used in such an environment.
Emissions
Test Compliance Electromagnetic Environment-
Guidance
RF emissions
CISPR 11
Group 1
The device uses RF energy only for its
internal function. Therefore, its RF
emissions are very low and are not
likely to cause any interference in
nearby electronic equipment
RF emissions
CISPR 11
Class B
The device is suitable for use in all
establishments, including domestic
establishments and those directly
connected to the public low-voltage
power supply network.
Harmonic
emissions
IEC61000-3-2
Class A
Voltage
fluctuations
/ Flicker
emissions
IEC61000-3-3
Complies
Warning:
1. The device should not be used adjacent to or stacked with other
equipment.
If adjacent or stacked use is necessary, the device should be
observed to verify normal operation in the configuration in which it
will be used.
2. Use of accessories, transducers and cables other than those
specified or provided by the manufacturer of this equipment could
result in increased electromagnetic emissions or decreased
electromagnetic immunity of this equipment and result in
improper operation.
3. Portable RF communications equipment (including peripherals
such as antenna cables and external antennas) should be used no
closer than 30 cm (12 inches)
to any part of the
Compressor, including cables specified by the
manufacturer. Otherwise, degradation of the performance of this
equipment could result.
Guidance and Manufacturer’s Declaration-
Electromagnetic Immunity:
This device is intended for use in the electromagnetic
environment specified below. The user of this device
should make sure it is used in such an environment.
Immunity Test
IEC60601
test level Compliance Electromagnetic
Environment-Guidance
Electrostatic
Discharge
(ESD)
IEC61000-4-2
±8kV contact
±15kV air
±8kV
contact
±15kV air
Floors should be
wood, concrete or
ceramic tile. If floors
are covered with
synthetic material,
800987 Rev H (Side 2) 666001-6720 V1.5
outlet connector.
5. Assemble the nebulizer cup and add indicated
medication to the nebulizer’s cup before use.
6. Attach the other end of the tubing into the air-inlet
connector founded at the bottom of the nebulizer cup.
7. Turn on the Salter AIRE
Elite
Compressor by
pressing the power switch to the I (ON) position
and begin treatment.
8. If treatment needs to be interrupted, simply press
power switch to O (OFF) position.
9. When the treatment is complete, turn off the
compressor by pressing the power switch to O (OFF)
position and unplug the unit from the electrical outlet.
Equipment is not suitable for use in the presence
of a flammable anesthetic mixture with air or with
oxygen or nitrous oxide. This device has no AP or APG
protection.
CAUTION During the treatment, the patient should not
touch the outer case due to expected rise in unit
temperature.
4.2 Safety Overload
NOTE Do not exceed 30 minutes of continuous operation.
1. The motor of this device has a built-in thermal overload
protector. Should the motor overheat, the protector will
automatically shut off the motor. Should this occur, turn
the I/O (ON/OFF) switch to the O (OFF) position and
allow the motor to cool down for approximately 30
minutes before turn it on again.
2. If the overload protector shuts off the motor frequently,
you may have an unstable voltage situation.
3. If the unit shuts down and cannot restart, it may need
to be replaced. Call your provider immediately.
5. Cleaning
5.1 Compressor Outer Case Cleaning
WARNING Electric shock hazard. Do not remove outer case
of this unit. All disassembly and maintenance of this unit
must be done by a qualified service technician. Refer
servicing to qualified service personnel.
WARNING This unit does not require oil. Do not attempt to
lubricate any internal parts.
WARNING Unplug unit before cleaning. Do not submerge in
water for cleaning.
1. Wipe the main unit with a damp cloth every few days to
keep it dust-free.
2. Do not use any powdered type cleaners or soap. Do not
submerge the unit into water.
5.2. Nebulizer Cup Cleaning
Clean the nebulizer after each use. Refer to the cleaning
instructions supplied with your nebulizer
WARNING To prevent possible risk of infection from
contaminated medication, cleaning of the nebulizer is
recommended after each treatment.
NOTE The nebulizer kit is for single patient use only.
NOTE Please follow national requirements to dispose the
unit properly.
6. Storage
Keep the unit and accessories dry. Avoid direct sunshine.
See specifications in Section 10 for appropriate
environmental storage conditions.
7. Maintenance
7.1 General Information
1. This unit is oil-less. Do Not Lubricate.
2. Risk of electric shock. Do not disassemble the main unit.
7.2 Filter Change
NOTE Inspect the filter once every month
and replace as necessary or when filter
turns gray. Please follow the below
instructions as right figures.
1. Open the filter cap.
2. Inspect the filter and if dirty, remove
filter with a small, pointed object.
Discard the filter.
3. Replace with a clean filter. Additional
filters should be purchased from your
provider.
4. Put the filter cap back.
CAUTION Do not use cotton or any other material as a filter.
Do not wash or reuse the filter. Do not operate the unit
without
a filter.
7.3 Service
Except for the above instructed user maintenance, all device
servicing must be performed by a Salter Labs®authorized
service representative. There are no serviceable parts inside
the unit. Contact your Salter Labs dealer or authorized
service center if your unit needs repair.
WARNING Do not tamper with or attempt to repair the
device. Refer servicing to qualified service personnel.
8. Expected Service Life
The products are intended to offer safe and reliable
operation when used or installed according to the
instructions provided by Salter Labs. Salter Labs
recommends that the system be inspected and serviced by
authorized technicians if there are any signs of wear or
concerns with device function and indication on products.
Otherwise, service and inspection of the devices generally
should not be required.
9. Troubleshooting
If your Salter AIRE
Elite
Compressor fails to function,
consult the Troubleshooting guide below. If the problem
persists, consult your equipment provider.
Problem Cause and Solution
Device doesn’t
operate
•Check if plug is properly fit into an
appropriate electrical outlet.
•When device has been run continuously for
over 30 minutes right before using, an auto
shut down may activate by built-in thermal
protector, cool down device for 30 minutes
before next usage.
Weak
Nebulization
•Check for proper electrical voltage.
•Check tubing for blockage or air leakage at
connection to Salter AIRE
Elite
Compressor
or nebulizer cup, replace
as needed.
•Check the nebulizer cup if it is properly
assembled and not damaged. If there is any
damage, replace as needed.
•Check if filter is too dirty, replace
as needed.
10. Specifications
(All specifications are subject to change without notice.)
Electrical Rating
(Note: Refer to the rating
label on the product)
120VAC,60Hz,1.2A
(For 120V System)
230VAC, 50Hz,
0.6A (For 230V
System)
Maximum Compressor
Pressure
≧30 psi
Nebulizer Flow Rate
≧
5.5 lpm
≧
5.0 lpm
Classification
Class II.
BF equipment.
IP2X
No AP/APG protection.
Applied part
Mouthpiece or Nasal mask
Dimensions (W x D x H)
14.6 × 20.3 × 9.5 cm /
5.7” × 7.9” × 3.7”
Weight (approx.)
1.8 kg / 4.0 lb
Fuse (non-user serviceable)
F5AL 250V
T1.6AL 250V
Expected Service Life
3 Years (minimum)
Warranty
5 Years
Environment
Temperature
Operation: 10
℃
to 40
℃
/ 50
℉
to 104
℉
Storage: -15
℃
to 50
℃
/ 5
℉
to 122
℉
Transport: -15
℃
to 70
℃
/ 5
℉
to 158
℉
Humidity
Operation: 10% to 90%RH
non-condensing
Storage: 10% to 90%RH
non-condensing
Transport: 10% to 90% RH
non-condensing
Atmospheric
Pressure
Operation: 700-1060 hPa
11. Accessories
Model Description
8501-1-2 Salter AIRE Elite Replacement filters
8258-0-1 Compressor Carrying bag
8660 NebuTech® Nebulizer – Reusable
8960 NebuTech Nebulizer – Disposable
8967 NebuTech Nebulizer with Pediatric Mask
8984 NebuTech Nebulizer with Adult Mask
8900 Nebulizer with Tee Adapter
8906 Nebulizer with Pediatric Mask
8924 Nebulizer with Adult Mask
12. Appendix A: EMC Information
Guidance and Manufacturer’s Declaration-
Electromagnetic Emissions:
This device is intended for use in the electromagnetic
environment specified below. The user of this device
should make sure it is used in such an environment.
Emissions
Test Compliance Electromagnetic Environment-
Guidance
RF emissions
CISPR 11
Group 1
The device uses RF energy only for its
internal function. Therefore, its RF
emissions are very low and are not
likely to cause any interference in
nearby electronic equipment
RF emissions
CISPR 11
Class B
The device is suitable for use in all
establishments, including domestic
establishments and those directly
connected to the public low-voltage
power supply network.
Harmonic
emissions
IEC61000-3-2
Class A
Voltage
fluctuations
/ Flicker
emissions
IEC61000-3-3
Complies
Warning:
1. The device should not be used adjacent to or stacked with other
equipment.
If adjacent or stacked use is necessary, the device should be
observed to verify normal operation in the configuration in which it
will be used.
2. Use of accessories, transducers and cables other than those
specified or provided by the manufacturer of this equipment could
result in increased electromagnetic emissions or decreased
electromagnetic immunity of this equipment and result in
improper operation.
3. Portable RF communications equipment (including peripherals
such as antenna cables and external antennas) should be used no
closer than 30 cm (12 inches)
to any part of the
Compressor, including cables specified by the
manufacturer. Otherwise, degradation of the performance of this
equipment could result.
Guidance and Manufacturer’s Declaration-
Electromagnetic Immunity:
This device is intended for use in the electromagnetic
environment specified below. The user of this device
should make sure it is used in such an environment.
Immunity Test
IEC60601
test level Compliance Electromagnetic
Environment-Guidance
Electrostatic
Discharge
(ESD)
IEC61000-4-2
±8kV contact
±15kV air
±8kV
contact
±15kV air
Floors should be
wood, concrete or
ceramic tile. If floors
are covered with
synthetic material,
800987 Rev H (Appendix A)
the relative humidity
should be at least
30%.
Electrical fast
transient/
burst
IEC61000-4-4
±2kV for
power supply
line
±1kV for
input/out line
±2kV for
power
supply line
±1kV for
input/out
line
Mains power quality
should be that of a
typical commercial or
hospital environment.
Surge
IEC61000-4-5
± 1 kV line(s)
to line(s)
± 2 kV line(s)
to earth
± 1 kV line(s)
to
line(s)
Mains power quality
should be that of a
typical commercial or
hospital environment.
Voltage dips,
short
interruptions
and voltage
variations on
power supply
input lines
IEC61000-4-
11
Voltage Dips:
i) 100%
reduction for
0.5 period,
ii) 100%
reduction for 1
period,
iii) 30%
reduction for
25/30 period,
Voltage
Interruptions:
100% reduction
for 250/300
period
Voltage Dips:
i) 100%
reduction for
0.5 period,
ii) 100%
reduction for
1 period,
iii) 30%
reduction for
25/30 period,
Voltage
Interruptions:
100%
reduction for
250/300
period
Mains power quality
should be that of a
typical commercial or
hospital environment.
If the user of this
device requires
continued operation
during power mains
interruptions, it is
recommended that
the device be powered
from an
uninterruptible power
supply or a battery.
Power
frequency
(50/60Hz)
magnetic
field
IEC61000-4-8
30 A/m 30 A/m
Power frequency
magnetic fields
should
be at levels
characteristic of a
typical location in a
typical commercial or
hospital environment.
NOTE: U
T
is the AC mains voltage prior to the application of the
test level
800987 Rev H (Side 2) 666001-6720 V1.5
Recommended separation distances between portable and
mobile RF communications equipment and this device:
This device is intended for use in an electromagnetic
environment in which radiated RF disturbances are controlled.
The customer or the user of this device can help prevent
electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications
equipment (transmitters) and this device as recommended
below, according to the maximum output power of the
communications equipment.
Rated
maximum
output
power
Separation distance according to frequency of transmitter (m)
150 kHz to 80
MHz
Pd =
80 MHz to 800 MHz
Pd 6.0=
800 MHz to 2,7 GHz
Pd 2.1=
0.01
0.1
0.06
0.12
0.1
0.31
0.19
0.38
1
1
0.6
1.2
10
3.1
1.9
3.8
100
10
6
12
For transmitters rated at a maximum output power not listed above, the
recommended separation distance
d
in meters (m) can be estimated using
the equation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to
the transmitter manufacturer.
Note 1: At 80 MHz and 800 MHz, the separation distance for the higher
frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures,
objects, and people.
Guidance and Manufacturer’s Declaration - Electromagnetic Immunity:
This device is intended for use in the electromagnetic
environment specified below. The user of this device should
make sure it is used in such an environment.
Immunity
Test
IEC60601
test level
Compliance
Electromagnetic Environment-
Guidance
Conducte
d RF
IEC 61000-
4-6
Radiated
RF
IEC 61000-
4-3
3Vrms
150 kHz to 80
MHz
6Vrms
ISM bandsa
Between 150
kHz to 80
MHz
80% AM at
1kHZ
10 V/m
80 MHz to
2.7GHz 80%
AM at 1kHZ
385-6000 MHz,
9-28V/m, 80%
AM (1kHz)
pulse mode
and other
modulation
3Vrms
150 kHz to
80 MHz
6Vrms
ISM
bandsa
Between
150 kHz to
80 MHz
80% AM at
1kHZ
10 V/m
80 MHz
to 2.7GHz
80% AM
at 1kHZ
385-6000
MHz, 9-
28V/m, 80%
AM (1kHz)
pulse mode
and other
modulation
Portable and mobile RF
communications equipment
should be used no closer to
any part of this device,
including cables, than there
commended separation
distance calculated from the
equation applicable to the
frequency of the transmitter.
Recommended separation
distance
Pd =
150 kHz to 80 MHz
Pd 6.0=
80 MHz to 800
MHz
Pd 2.1=
800 MHz to 2,7GHz
Where P is the maximum
output power rating of the
transmitter in watts (W)
according to the transmitter
manufacturer and d is the
recommended separation
distance in meters (m).
Field strengths from fixed RF
transmitters, as determined
by an electromagnetic site
survey a should be less than
the compliance level in each
frequency ranged.
Interference may occur in
the vicinity of equipment
marked with the following
symbol:
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range
applies.
NOTE 2: These guidelines may not apply in all situations.
Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
a/ Field strengths from fixed transmitters, such as base stations
for radio (cellular/cordless) telephones and land mobile radios,
amateur radio, AM and FM radio broadcast and TV broadcast
cannot be predicted theoretically with accuracy. To assess the
electromagnetic environment due to fixed RF transmitters, an
electromagnetic site survey should be considered. If the
measured field strength in the location in which the device is
used exceeds the applicable RF compliance level above, the
device should be observed to verify normal operation. If
abnormal performance is observed, additional measures may be
necessary, such as reorienting or relocating the device.
b/ Over the frequency range 150 kHz to 80 MHz, field strengths
should be less than 10/m.
Manufacturer’s declaration-electromagnetic immunity
Test specifications for ENCLOSURE PORT IMMUNITY to RF
wireless communications equipment
The 9R-029003(8353-1) is intended for use in the electromagnetic
environment (for home healthcare) specified below.
The customer or the user of the 9R-029003(8353-1) should assure
that it is used in such an environment.
Test frequency
(MHz)
Band a)
(MHz)
Service a)
Modulation b)
Maximum power
(W)
Distance
(m)
Immunity Test
Level
(V/m)
Compliance Level
(V/m)
(for home
385 380 –
390 TETRA 400
Pulse
modulati
on b)
18 Hz
1,8 0,3 27 27
450 430 –
470
GMRS 460,
FRS 460
FM c)
±5 kHz
deviatio
n
1 kHz
sine
2 0,3 28 28
710
704 –
787
LTE Band
13,
17
Pulse
modulati
on b)
217 Hz
0,2 0,3 9 9
745
780
810
800 –
960
GSM
800/900,T
ETRA 800,
iDEN 820,
CDMA
850,
LTE Band
5
Pulse
modulati
on b)
18 Hz
2 0,3 28 28
870
930
1
720
1 700 –
1 990
GSM 1800;
CDMA
1900;
GSM 1900;
DECT;
LTE Band
1, 3,
4, 25;
UMTS
Pulse
modulati
on b)
217 Hz
2 0,3 28 28
1
845
1
970
2
450
2 400 –
2 570
Bluetooth
,
WLAN,
802.11
b/g/n,
RFID 2450,
LTE Band
7
Pulse
modulati
on b)
217 Hz
2 0,3 28 28
5
240
5 100 –
5 800
WLAN
802.11
a/n
Pulse
modulati
on b)
217 Hz
0,2
0.3
9 9
5
500
5
785
NOTE If necessary to achieve the IMMUNITY TEST LEVEL, the
distance between the transmitting antenna and the ME
EQUIPMENT or ME SYSTEM may be reduced to 1 m. The 1 m
test distance is permitted by IEC 61000-4-3.
a) For some services, only the uplink frequencies are
included.
b) The carrier shall be modulated using a 50 % duty cycle
square wave signal.
c) As an alternative to FM modulation, 50% pulse modulation
at 18Hz may be used because while it does not represent
actual modulation, it would be worst case.
30 Spur Drive
El Paso, TX, 79906 USA
30 Spur Drive
El Paso, TX, 79906 USA
Phone: 1-800-421-0024, 1-800-235-4203
Toll-Free Fax: 1-800-628-4690
E-mail: customercare@salterlabs.com
www.salterlabs.com
Authorized Representative in the E.U.:
MT Promedt Consulting GmbH
Altenhofstrasse 80
D-66386 St. Ingbert, Germany
NOTE Consult distributor(s) or EU representative(s)
for additional technical documents.
2797
800987 Rev H (Side 2) 666001-6720 V1.5
Recommended separation distances between portable and
mobile RF communications equipment and this device:
This device is intended for use in an electromagnetic
environment in which radiated RF disturbances are controlled.
The customer or the user of this device can help prevent
electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications
equipment (transmitters) and this device as recommended
below, according to the maximum output power of the
communications equipment.
Rated
maximum
output
power
Separation distance according to frequency of transmitter (m)
150 kHz to 80
MHz
Pd =
80 MHz to 800 MHz
Pd 6.0=
800 MHz to 2,7 GHz
Pd 2.1=
0.01
0.1
0.06
0.12
0.1
0.31
0.19
0.38
1
1
0.6
1.2
10
3.1
1.9
3.8
100
10
6
12
For transmitters rated at a maximum output power not listed above, the
recommended separation distance
d
in meters (m) can be estimated using
the equation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to
the transmitter manufacturer.
Note 1: At 80 MHz and 800 MHz, the separation distance for the higher
frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures,
objects, and people.
Guidance and Manufacturer’s Declaration - Electromagnetic Immunity:
This device is intended for use in the electromagnetic
environment specified below. The user of this device should
make sure it is used in such an environment.
Immunity
Test
IEC60601
test level
Compliance
Electromagnetic Environment-
Guidance
Conducte
d RF
IEC 61000-
4-6
Radiated
RF
IEC 61000-
4-3
3Vrms
150 kHz to 80
MHz
6Vrms
ISM bandsa
Between 150
kHz to 80
MHz
80% AM at
1kHZ
10 V/m
80 MHz to
2.7GHz 80%
AM at 1kHZ
385-6000 MHz,
9-28V/m, 80%
AM (1kHz)
pulse mode
and other
modulation
3Vrms
150 kHz to
80 MHz
6Vrms
ISM
bandsa
Between
150 kHz to
80 MHz
80% AM at
1kHZ
10 V/m
80 MHz
to 2.7GHz
80% AM
at 1kHZ
385-6000
MHz, 9-
28V/m, 80%
AM (1kHz)
pulse mode
and other
modulation
Portable and mobile RF
communications equipment
should be used no closer to
any part of this device,
including cables, than there
commended separation
distance calculated from the
equation applicable to the
frequency of the transmitter.
Recommended separation
distance
Pd =
150 kHz to 80 MHz
Pd 6.0=
80 MHz to 800
MHz
Pd 2.1=
800 MHz to 2,7GHz
Where P is the maximum
output power rating of the
transmitter in watts (W)
according to the transmitter
manufacturer and d is the
recommended separation
distance in meters (m).
Field strengths from fixed RF
transmitters, as determined
by an electromagnetic site
survey a should be less than
the compliance level in each
frequency ranged.
Interference may occur in
the vicinity of equipment
marked with the following
symbol:
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range
applies.
NOTE 2: These guidelines may not apply in all situations.
Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
a/ Field strengths from fixed transmitters, such as base stations
for radio (cellular/cordless) telephones and land mobile radios,
amateur radio, AM and FM radio broadcast and TV broadcast
cannot be predicted theoretically with accuracy. To assess the
electromagnetic environment due to fixed RF transmitters, an
electromagnetic site survey should be considered. If the
measured field strength in the location in which the device is
used exceeds the applicable RF compliance level above, the
device should be observed to verify normal operation. If
abnormal performance is observed, additional measures may be
necessary, such as reorienting or relocating the device.
b/ Over the frequency range 150 kHz to 80 MHz, field strengths
should be less than 10/m.
Manufacturer’s declaration-electromagnetic immunity
Test specifications for ENCLOSURE PORT IMMUNITY to RF
wireless communications equipment
The 9R-029003(8353-1) is intended for use in the electromagnetic
environment (for home healthcare) specified below.
The customer or the user of the 9R-029003(8353-1) should assure
that it is used in such an environment.
Test frequency
(MHz)
Band a)
(MHz)
Service a)
Modulation b)
Maximum power
(W)
Distance
(m)
Immunity Test
Level
(V/m)
Compliance Level
(V/m)
(for home
385 380 –
390 TETRA 400
Pulse
modulati
on b)
18 Hz
1,8 0,3 27 27
450 430 –
470
GMRS 460,
FRS 460
FM c)
±5 kHz
deviatio
n
1 kHz
sine
2 0,3 28 28
710
704 –
787
LTE Band
13,
17
Pulse
modulati
on b)
217 Hz
0,2 0,3 9 9
745
780
810
800 –
960
GSM
800/900,T
ETRA 800,
iDEN 820,
CDMA
850,
LTE Band
5
Pulse
modulati
on b)
18 Hz
2 0,3 28 28
870
930
1
720
1 700 –
1 990
GSM 1800;
CDMA
1900;
GSM 1900;
DECT;
LTE Band
1, 3,
4, 25;
UMTS
Pulse
modulati
on b)
217 Hz
2 0,3 28 28
1
845
1
970
2
450
2 400 –
2 570
Bluetooth
,
WLAN,
802.11
b/g/n,
RFID 2450,
LTE Band
7
Pulse
modulati
on b)
217 Hz
2 0,3 28 28
5
240
5 100 –
5 800
WLAN
802.11
a/n
Pulse
modulati
on b)
217 Hz
0,2
0.3
9 9
5
500
5
785
NOTE If necessary to achieve the IMMUNITY TEST LEVEL, the
distance between the transmitting antenna and the ME
EQUIPMENT or ME SYSTEM may be reduced to 1 m. The 1 m
test distance is permitted by IEC 61000-4-3.
a) For some services, only the uplink frequencies are
included.
b) The carrier shall be modulated using a 50 % duty cycle
square wave signal.
c) As an alternative to FM modulation, 50% pulse modulation
at 18Hz may be used because while it does not represent
actual modulation, it would be worst case.
30 Spur Drive
El Paso, TX, 79906 USA
30 Spur Drive
El Paso, TX, 79906 USA
Phone: 1-800-421-0024, 1-800-235-4203
Toll-Free Fax: 1-800-628-4690
E-mail: customercare@salterlabs.com
www.salterlabs.com
Authorized Representative in the E.U.:
MT Promedt Consulting GmbH
Altenhofstrasse 80
D-66386 St. Ingbert, Germany
NOTE Consult distributor(s) or EU representative(s)
for additional technical documents.
2797
800987 Rev H (Side 2) 666001-6720 V1.5
Recommended separation distances between portable and
mobile RF communications equipment and this device:
This device is intended for use in an electromagnetic
environment in which radiated RF disturbances are controlled.
The customer or the user of this device can help prevent
electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications
equipment (transmitters) and this device as recommended
below, according to the maximum output power of the
communications equipment.
Rated
maximum
output
power
Separation distance according to frequency of transmitter (m)
150 kHz to 80
MHz
Pd =
80 MHz to 800 MHz
Pd 6.0=
800 MHz to 2,7 GHz
Pd 2.1=
0.01
0.1
0.06
0.12
0.1
0.31
0.19
0.38
1
1
0.6
1.2
10
3.1
1.9
3.8
100
10
6
12
For transmitters rated at a maximum output power not listed above, the
recommended separation distance
d
in meters (m) can be estimated using
the equation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to
the transmitter manufacturer.
Note 1: At 80 MHz and 800 MHz, the separation distance for the higher
frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures,
objects, and people.
Guidance and Manufacturer’s Declaration - Electromagnetic Immunity:
This device is intended for use in the electromagnetic
environment specified below. The user of this device should
make sure it is used in such an environment.
Immunity
Test
IEC60601
test level
Compliance
Electromagnetic Environment-
Guidance
Conducte
d RF
IEC 61000-
4-6
Radiated
RF
IEC 61000-
4-3
3Vrms
150 kHz to 80
MHz
6Vrms
ISM bandsa
Between 150
kHz to 80
MHz
80% AM at
1kHZ
10 V/m
80 MHz to
2.7GHz 80%
AM at 1kHZ
385-6000 MHz,
9-28V/m, 80%
AM (1kHz)
pulse mode
and other
modulation
3Vrms
150 kHz to
80 MHz
6Vrms
ISM
bandsa
Between
150 kHz to
80 MHz
80% AM at
1kHZ
10 V/m
80 MHz
to 2.7GHz
80% AM
at 1kHZ
385-6000
MHz, 9-
28V/m, 80%
AM (1kHz)
pulse mode
and other
modulation
Portable and mobile RF
communications equipment
should be used no closer to
any part of this device,
including cables, than there
commended separation
distance calculated from the
equation applicable to the
frequency of the transmitter.
Recommended separation
distance
Pd =
150 kHz to 80 MHz
Pd 6.0=
80 MHz to 800
MHz
Pd 2.1=
800 MHz to 2,7GHz
Where P is the maximum
output power rating of the
transmitter in watts (W)
according to the transmitter
manufacturer and d is the
recommended separation
distance in meters (m).
Field strengths from fixed RF
transmitters, as determined
by an electromagnetic site
survey a should be less than
the compliance level in each
frequency ranged.
Interference may occur in
the vicinity of equipment
marked with the following
symbol:
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range
applies.
NOTE 2: These guidelines may not apply in all situations.
Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
a/ Field strengths from fixed transmitters, such as base stations
for radio (cellular/cordless) telephones and land mobile radios,
amateur radio, AM and FM radio broadcast and TV broadcast
cannot be predicted theoretically with accuracy. To assess the
electromagnetic environment due to fixed RF transmitters, an
electromagnetic site survey should be considered. If the
measured field strength in the location in which the device is
used exceeds the applicable RF compliance level above, the
device should be observed to verify normal operation. If
abnormal performance is observed, additional measures may be
necessary, such as reorienting or relocating the device.
b/ Over the frequency range 150 kHz to 80 MHz, field strengths
should be less than 10/m.
Manufacturer’s declaration-electromagnetic immunity
Test specifications for ENCLOSURE PORT IMMUNITY to RF
wireless communications equipment
The 9R-029003(8353-1) is intended for use in the electromagnetic
environment (for home healthcare) specified below.
The customer or the user of the 9R-029003(8353-1) should assure
that it is used in such an environment.
Test frequency
(MHz)
Band a)
(MHz)
Service a)
Modulation b)
Maximum power
(W)
Distance
(m)
Immunity Test
Level
(V/m)
Compliance Level
(V/m)
(for home
385 380 –
390 TETRA 400
Pulse
modulati
on b)
18 Hz
1,8 0,3 27 27
450 430 –
470
GMRS 460,
FRS 460
FM c)
±5 kHz
deviatio
n
1 kHz
sine
2 0,3 28 28
710
704 –
787
LTE Band
13,
17
Pulse
modulati
on b)
217 Hz
0,2 0,3 9 9
745
780
810
800 –
960
GSM
800/900,T
ETRA 800,
iDEN 820,
CDMA
850,
LTE Band
5
Pulse
modulati
on b)
18 Hz
2 0,3 28 28
870
930
1
720
1 700 –
1 990
GSM 1800;
CDMA
1900;
GSM 1900;
DECT;
LTE Band
1, 3,
4, 25;
UMTS
Pulse
modulati
on b)
217 Hz
2 0,3 28 28
1
845
1
970
2
450
2 400 –
2 570
Bluetooth
,
WLAN,
802.11
b/g/n,
RFID 2450,
LTE Band
7
Pulse
modulati
on b)
217 Hz
2 0,3 28 28
5
240
5 100 –
5 800
WLAN
802.11
a/n
Pulse
modulati
on b)
217 Hz
0,2
0.3
9 9
5
500
5
785
NOTE If necessary to achieve the IMMUNITY TEST LEVEL, the
distance between the transmitting antenna and the ME
EQUIPMENT or ME SYSTEM may be reduced to 1 m. The 1 m
test distance is permitted by IEC 61000-4-3.
a) For some services, only the uplink frequencies are
included.
b) The carrier shall be modulated using a 50 % duty cycle
square wave signal.
c) As an alternative to FM modulation, 50% pulse modulation
at 18Hz may be used because while it does not represent
actual modulation, it would be worst case.
30 Spur Drive
El Paso, TX, 79906 USA
30 Spur Drive
El Paso, TX, 79906 USA
Phone: 1-800-421-0024, 1-800-235-4203
Toll-Free Fax: 1-800-628-4690
E-mail: customercare@salterlabs.com
www.salterlabs.com
Authorized Representative in the E.U.:
MT Promedt Consulting GmbH
Altenhofstrasse 80
D-66386 St. Ingbert, Germany
NOTE Consult distributor(s) or EU representative(s)
for additional technical documents.
2797
800987 Rev H (Side 2) 666001-6720 V1.5
Recommended separation distances between portable and
mobile RF communications equipment and this device:
This device is intended for use in an electromagnetic
environment in which radiated RF disturbances are controlled.
The customer or the user of this device can help prevent
electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications
equipment (transmitters) and this device as recommended
below, according to the maximum output power of the
communications equipment.
Rated
maximum
output
power
Separation distance according to frequency of transmitter (m)
150 kHz to 80
MHz
Pd =
80 MHz to 800 MHz
Pd 6.0=
800 MHz to 2,7 GHz
Pd 2.1=
0.01
0.1
0.06
0.12
0.1
0.31
0.19
0.38
1
1
0.6
1.2
10
3.1
1.9
3.8
100
10
6
12
For transmitters rated at a maximum output power not listed above, the
recommended separation distance
d
in meters (m) can be estimated using
the equation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to
the transmitter manufacturer.
Note 1: At 80 MHz and 800 MHz, the separation distance for the higher
frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic
propagation is affected by absorption and reflection from structures,
objects, and people.
Guidance and Manufacturer’s Declaration - Electromagnetic Immunity:
This device is intended for use in the electromagnetic
environment specified below. The user of this device should
make sure it is used in such an environment.
Immunity
Test
IEC60601
test level
Compliance
Electromagnetic Environment-
Guidance
Conducte
d RF
IEC 61000-
4-6
Radiated
RF
IEC 61000-
4-3
3Vrms
150 kHz to 80
MHz
6Vrms
ISM bandsa
Between 150
kHz to 80
MHz
80% AM at
1kHZ
10 V/m
80 MHz to
2.7GHz 80%
AM at 1kHZ
385-6000 MHz,
9-28V/m, 80%
AM (1kHz)
pulse mode
and other
modulation
3Vrms
150 kHz to
80 MHz
6Vrms
ISM
bandsa
Between
150 kHz to
80 MHz
80% AM at
1kHZ
10 V/m
80 MHz
to 2.7GHz
80% AM
at 1kHZ
385-6000
MHz, 9-
28V/m, 80%
AM (1kHz)
pulse mode
and other
modulation
Portable and mobile RF
communications equipment
should be used no closer to
any part of this device,
including cables, than there
commended separation
distance calculated from the
equation applicable to the
frequency of the transmitter.
Recommended separation
distance
Pd =
150 kHz to 80 MHz
Pd 6.0=
80 MHz to 800
MHz
Pd 2.1=
800 MHz to 2,7GHz
Where P is the maximum
output power rating of the
transmitter in watts (W)
according to the transmitter
manufacturer and d is the
recommended separation
distance in meters (m).
Field strengths from fixed RF
transmitters, as determined
by an electromagnetic site
survey a should be less than
the compliance level in each
frequency ranged.
Interference may occur in
the vicinity of equipment
marked with the following
symbol:
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range
applies.
NOTE 2: These guidelines may not apply in all situations.
Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
a/ Field strengths from fixed transmitters, such as base stations
for radio (cellular/cordless) telephones and land mobile radios,
amateur radio, AM and FM radio broadcast and TV broadcast
cannot be predicted theoretically with accuracy. To assess the
electromagnetic environment due to fixed RF transmitters, an
electromagnetic site survey should be considered. If the
measured field strength in the location in which the device is
used exceeds the applicable RF compliance level above, the
device should be observed to verify normal operation. If
abnormal performance is observed, additional measures may be
necessary, such as reorienting or relocating the device.
b/ Over the frequency range 150 kHz to 80 MHz, field strengths
should be less than 10/m.
Manufacturer’s declaration-electromagnetic immunity
Test specifications for ENCLOSURE PORT IMMUNITY to RF
wireless communications equipment
The 9R-029003(8353-1) is intended for use in the electromagnetic
environment (for home healthcare) specified below.
The customer or the user of the 9R-029003(8353-1) should assure
that it is used in such an environment.
Test frequency
(MHz)
Band a)
(MHz)
Service a)
Modulation b)
Maximum power
(W)
Distance
(m)
Immunity Test
Level
(V/m)
Compliance Level
(V/m)
(for home
385 380 –
390 TETRA 400
Pulse
modulati
on b)
18 Hz
1,8 0,3 27 27
450 430 –
470
GMRS 460,
FRS 460
FM c)
±5 kHz
deviatio
n
1 kHz
sine
2 0,3 28 28
710
704 –
787
LTE Band
13,
17
Pulse
modulati
on b)
217 Hz
0,2 0,3 9 9
745
780
810
800 –
960
GSM
800/900,T
ETRA 800,
iDEN 820,
CDMA
850,
LTE Band
5
Pulse
modulati
on b)
18 Hz
2 0,3 28 28
870
930
1
720
1 700 –
1 990
GSM 1800;
CDMA
1900;
GSM 1900;
DECT;
LTE Band
1, 3,
4, 25;
UMTS
Pulse
modulati
on b)
217 Hz
2 0,3 28 28
1
845
1
970
2
450
2 400 –
2 570
Bluetooth
,
WLAN,
802.11
b/g/n,
RFID 2450,
LTE Band
7
Pulse
modulati
on b)
217 Hz
2 0,3 28 28
5
240
5 100 –
5 800
WLAN
802.11
a/n
Pulse
modulati
on b)
217 Hz
0,2
0.3
9 9
5
500
5
785
NOTE If necessary to achieve the IMMUNITY TEST LEVEL, the
distance between the transmitting antenna and the ME
EQUIPMENT or ME SYSTEM may be reduced to 1 m. The 1 m
test distance is permitted by IEC 61000-4-3.
a) For some services, only the uplink frequencies are
included.
b) The carrier shall be modulated using a 50 % duty cycle
square wave signal.
c) As an alternative to FM modulation, 50% pulse modulation
at 18Hz may be used because while it does not represent
actual modulation, it would be worst case.
30 Spur Drive
El Paso, TX, 79906 USA
30 Spur Drive
El Paso, TX, 79906 USA
Phone: 1-800-421-0024, 1-800-235-4203
Toll-Free Fax: 1-800-628-4690
E-mail: customercare@salterlabs.com
www.salterlabs.com
Authorized Representative in the E.U.:
MT Promedt Consulting GmbH
Altenhofstrasse 80
D-66386 St. Ingbert, Germany
NOTE Consult distributor(s) or EU representative(s)
for additional technical documents.
2797
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