Veridian Healthcare 11-511 User manual
INSTRUCTION MANUAL • ENGLISH & ESPAÑOL
MicroNeb Compressor
Nebulizer System
Model 11-511
Please read this instruction manual
completely before operating this unit.
3-YEAR 2-YEAR
3-YEAR 2-YEAR
1-YEAR
1-YEAR
2 • ENGLISH
Compressor Body Air Tubing Nebulizer Top, Cup
and Pickup Funnel
Angled
Mouthpiece
(5) Air Filters
Instruction Manual
FAQ Information Sheet
Replacement Parts
Order Form
Stop!
Please ensure you have all of the following
components before using your Nebulizer
IF YOU ARE MISSING ANY PARTS, INCLUDING INSERTS OR
INSTRUCTION MANUALS, DO NOT RETURN TO PLACE OF
PURCHASE. CONTACT CUSTOMER CARE AT 8663261313.
ENGLISH • 3
INDEX
Manufactured for:
Veridian Healthcare
1175 Lakeside Drive
Gurnee, IL 60031
www.veridianhealthcare.com
Made in China
#93-1290 09/20
©2020 Veridian Healthcare, LLC
Toll-Free Customer Care Help Line: 1-866-326-1313
Monday – Friday 8:30 a.m. – 4:30 p.m. CST
Care & Safety Information .....................................................................................4-5
Introduction..................................................................................................................6
Product Features..........................................................................................................7
Nebulizer Mask/Mouthpiece Selection..................................................................8
Using Your Nebulizer ........................................................................................... 9-11
Cleaning...................................................................................................................... 12
Changing the Filter .................................................................................................. 13
Troubleshooting ....................................................................................................... 14
Warnings & Cautions ............................................................................................... 15
Device Symbols......................................................................................................... 16
Electromagnetic Compatibility.......................................................................17-20
Product Specications............................................................................................. 21
Particle Size & Characterization ............................................................................ 22
Warranty ..................................................................................................................... 23
Instrucciones en Español..................................................................................25-48
NOTE: Read all instructions carefully before use. The following basic precautions are needed
when using an electrical product. Failure to read and observe all precautions could result in
personal injury or equipment damage.
Improper care or use of your nebulizer may result in injury, damage to the unit or
ineective treatment. Following these instructions will ensure the nebulizer’s ecacy
and long life.
GENERAL CAUTIONS AND WARNINGS
• Do not use the nebulizer for anything except medical nebulization treatment as directed
by a physician. Do not use the nebulizer in a manner inconsistent with these instructions.
• Never use any liquid in the nebulizer other than those prescribed by your doctor.
• Liquids such as cough medicines or essential oils can harm both the unit and patient.
• Do not disassemble the nebulizer or attempt to repair it; any attempt for repair should be
completed only by qualied technical personnel.
• The nebulizer is an electronic device, keep away from water to avoid electrical shock. Do
not immerse the unit in liquid and do not use while bathing. If the unit should fall into
water, do not reach for it without rst unplugging the unit.
• Do not use the unit if it has been dropped, exposed to extreme temperatures or high
humidity or damaged in any way.
• The mouthpiece should be replaced every 30 days.
• Modication of this device may void the warranty and is not allowed.
OPERATING CAUTIONS AND WARNINGS
• Never allow the nebulizer to be used without adult supervision; air tubing and small
accessories may post a choking hazard.
• Do not use the unit outdoors or in very dusty environments.
• Never use while sleeping or drowsy.
4 • ENGLISH
IMPORTANT
SAFEGUARDS
CARE & SAFETY INFORMATION
ENGLISH • 5
IMPORTANT
SAFEGUARDS
CARE & SAFETY INFORMATION
• Do not use while bathing or with wet hands.
• Do not use unit where aerosol products are being used or where oxygen, nitrous oxide or
anesthetics are being administered.
• The medicine liquid of usage and capacity must apply to doctor’s advice.
• Do not allow the nebulized medicine to come in contact with your eyes.
• Always ensure that the air vents are not blocked or obstructed in any way.
• If the nebulizer is not functioning correctly, if it makes unusual sounds, or if during use
you feel pain or discomfort, immediately stop use.
• Do not unplug the air tube during the treatment, otherwise may get injured because of
the eect of pressure.
• Do not bend the air tubing of the unit where the air tube may be obstructed.
• Always turn o and unplug the unit after use.
• Do not expose the unit to direct sunlight, heated or hot surfaces, humid environments,
extreme temperatures, strong static electricity or electromagnetic waves.
STORAGE CAUTIONS AND WARNINGS
• Do not store the unit in direct sunlight, high temperatures or humidity.
• Keep the unit out of reach of children.
• Always keep the unit unplugged when not in use.
CLEANING CAUTIONS AND WARNINGS
• Clean all necessary parts after each treatment as instructed in this manual; if the unit has
not been used for an extended period, all parts should be cleaned prior to use.
• Disconnect the unit from the electrical outlet before cleaning.
• Never immerse the unit in water to clean as it may damage the unit.
• Do not use abrasive cleaners.
6 • ENGLISH
INTRODUCTION
Thank you for purchasing a Compressor Nebulizer. Please read this instruction manual
completely before using your unit to ensure safe and eective use, as well as long life
of the product.
STATEMENT OF INTENDED USE
The aerosol generator is for the production of compressed air to operate a nebulizer for the
production of medical aerosol for respiratory disorders. The aerosol generator is used in
conjunction with a pneumatic nebulizer which nebulizes specic drugs for inhalation by a
patient and requires the order of a physician for medical use.
Only use included Veridian brand accessories; do not use accessories from other brands
or models. Reorder information is included throughout this manual and on the included
Replacement Parts Order Form.
WARNING: Federal law allows nebulizers to be sold by a physician’s prescription
only. These devices should be used only at the direction of a doctor or healthcare
professional and should be used only as intended and described in this manual.
ENGLISH • 7
PRODUCT FEATURES
Built-in
Nebulizer
Holder
Built-In
Handle
Power
Cord
All Veridian nebulizers include
a complete nebulizer kit –
angled mouthpiece, nebulizer,
air tubing and ve air lters. Air Tubing
Connector
Port
Air Vents
Power
Switch
8 • ENGLISH
NEBULIZER MASKS/MOUTHPIECE SELECTION
Angled mouthpiece
Tee adapter mouthpiece
Face mask
Pacier mouthpiece
This unit includes one standard angled mouthpiece. Additional styles of mouthpieces and
masks are available for order on the enclosed order form, by calling Customer Care at 866-326-
1313 or at your local medical supply dealer.
Proper use of the mouthpiece is
important in helping to ensure eective
and ecient medication delivery.
Angled mouthpiece (included): put the
mouthpiece into the mouth, holding
gently between the teeth and close the
lips around the mouthpiece; hold the
nebulizer in place with a free hand.
Face mask (not included): select the
appropriate size for the patient - child or
adult - and place over the patients nose
and mouth. Secure in place with the
elastic strap around the patient’s
head and hold the nebulizer in
place with a free hand.
Tee adapter mouthpiece (not
included): put the mouthpiece end
into the mouth, holding gently
between the teeth and close the
lips around the mouthpiece; hold
the nebulizer in place with a free
hand.
Pacier mouthpiece (not
included): put the pacier nipple
into the baby’s mouth; an adult
should hold the nebulizer, being certain
the medicine cup remains upright.
ENGLISH • 9
USING YOUR NEBULIZER
Before the rst use of the nebulizer or if the unit has not been used for an extended period of
time, it should be cleaned thoroughly as described in the Cleaning section of this manual.
The patient receiving treatment should be seated or slightly reclined in a comfortable position
as treatments take several minutes. Keep in mind that
the nebulizer cup must remain vertical during treatment.
1. Place the compressor unit on a at, stable surface
within operating range of the patient and an
electrical outlet. Ensure that the air vents on
the side of the unit housing are not blocked or
obstructed and that the power is o.
2. Plug the power cord into the electrical outlet.
3. Attach one end of the air tube to the tube
connector at the back of the unit, Fig. 1. Turn on the
power briey to ensure that the unit is functioning
properly and test that air is coming through the
tubing, then turn the power o.
Disposable Nebulizer (INCLUDED)
This unit is intended for single patient use and should not be shared with other
people. This nebulizer should be replaced every 30 days.
Be sure to inspect the nebulizer for damage before each use.
Fig. 1
10 • ENGLISH
USING YOUR NEBULIZER
4. Fill and assemble the
nebulizer.
Step 1: Make sure the pick-
up funnel is in place in the
bottom half of the nebulizer.
Step 2: Pour the medication
into the nebulizer cup
following the physician
prescribed dosage, Fig 2.
Step 3: Replace the top of the
nebulizer and twist to close;
gently pull the top to ensure
the top is secure, Fig 3.
5. Attach the selected
mouthpiece to the top of the
nebulizer, taking care not to
spill the medication in the
cup, Fig 4.
6. Attach the nebulizer to the
air tubing, Fig 5.
Treatment time varies depending on the type of medication and
volume of medication being used. It is important to complete the entire
prescribed dose of medication for maximum eectiveness. Consult with
your prescribing physician or healthcare professional for information on
your specic medication therapy treatment plan.
Fig. 4 Fig. 5
Fig. 3Fig. 2
ENGLISH • 11
USING YOUR NEBULIZER
IF THE VAPOR BEGINS TO SLOW AND THERE IS STILL MEDICATION IN
THE CUP, GENTLY TAP THE SIDE OF THE CUP TO SETTLE THE LIQUID AT
THE BOTTOM OF THE CUP FOR NEBULIZATION.
Mouthpiece position
7. Position the mouthpiece at the patient’s mouth.
Remember that, mouthpieces should be in the mouth with
the lips closed around the end of the mouthpiece.
8. Turn the power switch to the on ( I) position to begin
treatment. Inhale deeply and exhale normally. Ensure the
nebulizer is vertical during treatment for proper nebulization
of the medication and to prevent spilling of the liquid.
9. If the vapor output becomes sporadic or if the noise the unit
makes changes during use, turn o the unit and consult the
TROUBLESHOOTING section of this instruction manual.
10. When the treatment is complete, turn the unit o and
unplug it from the outlet.
11. Disassemble, clean and store your nebulizer. Be certain that
the nebulizer pieces are completely dry before storage.
12 • ENGLISH
All parts of this nebulizer (excluding air tubing) should be cleaned according to the below
instructions. A dierent cleaning regimen may be specied by your healthcare professional;
additional hygienic precautions may be required for use with high-risk patients.
The masks, mouthpieces, tubing and nebulizer are not dishwasher safe. The below instructions
are for manual cleaning.
Nebulizer and Components Cleaning:
1. Ensure that the power cord is disconnected
from the power outlet.
2. Disconnect the air tube, nebulizer and
mouthpiece. Do not wash or submerge tubing.
3. Disassemble the nebulizer by twisting the top
and bottom and separating the pieces, Fig 1-2.
4. RInse the nebulizer and mouthpiece in running
water. Clean the nebulizer with warm, soapy
water. Then rinse pieces again to remove all
residue.
5. Allow nebulizer and all parts to dry completely; store in a clean plastic bag or container.
Compressor Body Cleaning:
1. Ensure that the power cord is disconnected from the power outlet.
2. Wipe the outside of the compressor body with a clean, damp cloth
CAUTION: Do not use any powdered cleaners or soap pads which may damage the unit.
WARNING: Do not submerge the compressor in water; do so will result in compressor damage
and void the warranty.
Nebulizers and tubing should be replaced as needed depending on the frequency of therapy
treatments or when damaged, cracked or holes appear in the tubing. To order replacement
parts, use the included order form, call Customer Care at 866-326-1313 or your local dealer.
CLEANING
Fig. 2Fig. 1
ENGLISH • 13
CHANGING THE FILTER
• Change lter every 30 days or when the lter turns gray
• CAUTION: Never operate the unit without a lter.
• CAUTION: Do not substitute cotton or any other materials for the lters.
• CAUTION: Do not attempt to clean the lters or reuse a lter.
• Use only Veridian Healthcare lters; additional lters are available for order using the
included order form, calling Customer Care at 866-326-1313 or contacting your local
dealer.
To replace the lter, follow these steps:
1. Change the lter only when the unit is
o, unplugged and completely cool.
2. Gently pull the lter cap out of the
compressor.
3. Remove the lter from the lter cap.
4. Place a new lter in the lter cap.
5. Return the lter cap to its place,
ensuring that it is rmly in place.
14 • ENGLISH
TROUBLESHOOTING
The nebulizer produces no aerosol, or a small amount of aerosol.
• There may be too much or too little medicine in the nebulizer. The amount of liquid
should be between 2 ml and 8 ml.
• The hose connectors may be blocked and need to be cleaned
• The nebulizer may not be held upright. Always hold the nebulizer vertically during use.
• The medication may not be suitable for nebulization. Check with your doctor.
• The lter may be in need of replacement
• The air hose may be kinked
Some medicine remains in the nebulizer at the end of my treatment.
This is normal. Once you hear a signicant dierence in the sound of the nebulizer, you may
stop inhaling.
What medications can be used in the nebulizer?
Only medications prescribed by your doctor should be used in the nebulizer.
Should any special steps be taken for pediatric users?
Children should never use the nebulizer without adult supervision. For use with babies
and children, the mask should cover the mouth and nose completely to ensure eective
inhalation.
Can I share the nebulizer with another person?
No. Each user must have their own nebulizer to ensure proper hygiene. The compressor unit
may be shared but the nebulizer mouthpiece, and mask pieces may not.
Why must the nebulizer be replaced every 30 days?
Regular wear on the nebulizer can aect the composition and delivery of the medicine.
Regular replacement of the nebulizer is also hygienic.
ENGLISH • 15
WARNING & CAUTIONS
Nebulizer therapy is intended for use with physician prescribed medication only.
Over the counter medication, essential/aromatherapy oils or alcohol are not suitable for
inhaling using a nebulizer. Highly viscous substances may damage the unit and make it
unsuitable for use. Never use nebulizer therapy for anything other than physician prescribed
respiratory care therapy.
Use common sense electrical caution when operating the device. This nebulizer runs on
AC power. Always turn o the power and unplug the device before cleaning or if the unit is
not working properly.
Compressor nebulizers contain a powerful compressor motor which may heat up the unit if it
is left running too long or if the vents are blocked while operating. The unit will automatically
shut o if the temperature of the unit becomes too high. Contact Customer Care for assistance
if the device fails to operate.
16 • ENGLISH
These symbols may appear on your device, instructions or packaging and may vary by make
and model.
Read This Manual—All included manuals should be read prior to rst use
Warning—Symbol indicates a warning, prohibition or mandatory action that
mitigates a risk that is not necessarily obvious to the device operator
Type BF Applied Parts—Indicates that a part of this unit comes in contact with the
patient in order to carry out it’s intended function
Environment Protection—dispose of this product properly; consult with your local
recycling ordinances for proper recycling and disposal
IP21—Protected against foreign objects equal to or greater than 12.5 mm in
diameter and against vertically falling drops of water
Double Insulation—This unit is double-protected and thus cooresponds to
protection class 2
POWER ON — Line is ON
POWER OFF — Circle is OFF
Alternating Current
Serial Number
Rx Only — Federal Law restricts this device to sale by or on the order of a
physician
Symbol Meaning
2012
WARNING AND CAUTIONS—DEVICE SYMBOLS
ENGLISH • 17
ELECTROMAGNETIC COMPATIBILITY
Table 1
For all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacture’s declaration - electromagnetic emissions
This device is intended for use in the electromagnetic environment specied below. The customer or the user of this device should assure that it is used in such an environment.
Emmission Test Compliance Electromagnetic Environment Guidance
Group 1
Class B
Class A
Complies
This 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.
This device is suitable for use in all establishments, including domestic establishments and those directly connected to
the public low-voltage power supply network that supplies buildings used for domestic purposes.
RF emissions
CISPR 11
RF emissions
CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage uctuations/icker emissions
IEC 61000-3-3
Table 2
For all ME EQUIPMENT and ME SYSTEMS
Guidance and manufacture’s declaration - electromagnetic immunity
This device is intended for use in the electromagnetic environment specied below. The customer or the user of this device should assure that it is used in such an environment.
Electrostatic discharge (ESD)
IEC 61000-4-2
Electrical fast
transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage dips, short
interruptions and voltage
variations
on power supply
input lines
IEC 61000-4-11
Power frequency (50/60 Hz)
magnetic eld
IEC 61000-4-8
± 8 kV contact
± 15 kV air
± 2 kV for power supply lines
± 1 kV for input/output lines
line(s) to line(s):
±1 kV. line(s) to earth:
±2 kV. 100 kHz repetition frequency
5% UT (>95% dip in UT)
for 0.5 cycle 40% UT (60% dip in UT)
for 5 cycle 70% UT (30% dip in UT)
for 25 cycle <5% UT (>95% dip in UT)
for 5s
3 A/m
50Hz/60Hz
± 8 kV contact
± 15 kV air
± 2 kV for power supply lines
± 1 kV line(s) to line(s)
± 2 kV line(s) to earth
5% UT (>95% dip in UT)
for 0.5 cycle 40% UT (60% dip in UT)
for 5 cycle 70% UT (30% dip in UT)
for 25 cycle <5% UT (>95% dip in UT)
for 5s
3 A/m
50Hz/60Hz
Floors should be wood, concrete or ceramic tile. If oors are covered with
synthetic material, the relative humidity should be at least 30 %.
Mains power quality should be that of a typical commercial or hospital
environment.
Mains power quality should be that of a typical commercial or hospital
environment.
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 this device be powered
from an uninterruptible power supply or a battery.
Power frequency magnetic elds should be at levels characteristic of a
typical location in a typical commercial or hospital environment.
Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment Guidance
18 • ENGLISH
ELECTROMAGNETIC COMPATIBILITY
Table 3
Guidance and manufacturer’s declaration - electromagnetic immunity
This device is intended for use in the electromagnetic environment specied below. The customer or the user of this device should assure that it is used in such an environment.
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
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 reection from structures, objects and people.
* Field strengths from xed 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 xed RF transmitters, an
electromagnetic site survey should be considered. If the measured eld strength in the location in which this device is used exceeds the applicable RF compliance level
above, this device should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting
or relocating this device.
** Over the frequency range 150 kHz to 80 MHz, eld strengths should be less than 3V/m.
150KHz to 80MHz:
3Vrms 6Vrms (in ISM and amateur radio
bands) 80% Am at 1kHz
10V/m
150KHz to 80MHz:
3Vrms 6Vrms (in ISM and
amateur radio bands) 80%
Am at 1kHz
10V/m
Portable and mobile RF communications equipment should be used no closer
to any part of this device, including cables, than the recommended separation
distance calculated from the equation applicable to the frequency of the
transmitter.
Recommended separation distance:
Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment Guidance
d = 2.3
1
d = 2.
d = 2
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 xed RF transmitters, as
determined by an electromagnetic site survey,*
should be less than the compliance level in each
frequency range.** Interference may occur in
the vicinity of equipment marked with
the following symbol:
80MHz to 800MHz:
d=1.2√P;
800MHz to 2.7GHz:
d=2.3√P
ENGLISH • 19
ELECTROMAGNETIC COMPATIBILITY
Table 4
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.
0.2
0.632
2
6.32
20
0.23
0.73
2.3
7.3
23
1
d = 2.
1
d = 2.
d = 2.3
d = 2.3
0,01
0,1
1
10
100
0.12
0.38
1.2
3.8
12
0.12
0.38
1.2
3.8
12
150 kHz to 80 MHz (out ISM
and amateur radio bands) 150 kHz to 80 MHz (in ISM
and amateur radio bands) 80MHz to 800MHz 80MHz to 800MHz
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be determined 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 reection from structures, objects and people.
Separation distance according to frequency of transmitter m
Rated maximum output
power of transmitter
W
20 • ENGLISH
ELECTROMAGNETIC COMPATIBILITY
Table 5
Guidance and manufacturer’s declaration - electromagnetic immunity
The Device is intended for use in the electromagnetic environment specied below. The user of the Device should assure that it is used in such an environment.
Test Band Service Modulation Modulation Distance Immunity
frequency (MHz) (W) (m) test levels
(MHz) (V/m)
380-390
430-470
704-787
800-960
1700-1990
2400-2570
5100-5800
TETRA 400
GMRS 460,
FRS 460
LTE Band
13, 17
GSM 800/900,
TETRA 800, iDEN 820,
CDMA 850, LTE
Band 5
GSM 1800;
CDMA 1900;
GSM 1900;
DECT; LTE Band 1,
3, 4,25; UMTS
Bluetooth, WLAN,
802.11 b/g/n, RFID
2450, LTE Band 7
WLAN
802.11
a/n
Pulse modulation
b) 18Hz
FM, ±5kHz deviation,
1kHz sine
Pulse modulation
b) 217Hz
Pulse modulation
b) 18Hz
Pulse modulation
b) 217Hz
Pulse modulation
b) 217Hz
Pulse modulation
b) 217Hz
1.8
2
0.2
2
2
2
0.2
0.3
0.3
0.3
0.3
0.3
0.3
0.3
27
28
9
28
28
28
9
Radiated RF
IEC61000-4-3
(Test
specications
for
ENCLOSURE
PORT
IMMUNITY to
RF wireless
communications
equipment)
385
450
710
745
780
810
870
930
1720
1845
1970
2450
5240
5500
5785
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 18 Hz may be used because while it does not represent actual modulation, it would be worst case.
The MANUFACTURER should consider reducing the minimum separation distance, based on RISK MANAGEMENT, and using higher IMMUNITY TEST LEVELS that are appropriate for the reduced minimum
separation distance. Minimum separation distances for higher IMMUNITY TEST LEVELS shall be calculated using the following equation:
Where P is the maximum power in W, d is the minimum separation distance in m, and E is the IMMUNITY TEST LEVEL in V/m.
E
=
6
d
Table of contents
Languages:
Other Veridian Healthcare Respiratory Product manuals
