Drive Medquip MQ5800 Manual

Sistema de Compresor Guía de Instrucciones
Nebulizador
Modelo MQ5800, MQ5900, MQ5900P
Système de Compresseur Guide d’Instructions
Nébuliseur
Modèles MQ5800, MQ5900, MQ5900P
Caution– Federal (U.S.A.) law
restricts this device to sale by, or
on the order of a physician.
Made in China. Latex Free.
Precaucion– La ley federal (EE.
UU.) restringe la venta de este
aparato para ser realizada por, o
bajo prescripción de, un médico.
Hecho en China. No Contiene
Látex.
Attention– La loi fédérale (États-
Unis) limite la vente de ce
dispositif par ou sur ordonnance
d’un médecin.
Fabriqué aux China. Garanti sans
Compressor Nebulizer
System
Model MQ5800, MQ5900, MQ5900P
Instruction
Guide

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DRIVE COMPRESSOR/NEBULIZER MODEL MQ5800, MQ5900, MQ5900P
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2
table of contents
TABLE OF CONTENTS
Important Safeguards...........................................................4
IEC Symbols........................................................................4
Important Safeguards..........................................................4
Introduction...........................................................................6
Statement Of Intended Use.................................................6
What Are Compressor Nebulizer Systems Used For?.........6
How Does A Compressor Nebulizer Work?.........................6
How Do I Take A Treatment?...............................................7
Product Identification
and Available Accessories...................................................8
Operation...............................................................................9
How To Operate Your Compressor......................................9
Cleaning & Maintenance....................................................11
Nebulizer Cleaning.............................................................11
Compressor Cleaning........................................................12
Filter Change.....................................................................12
Maintenance......................................................................12
Specifications......................................................................13
Limited Warranty.................................................................19

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ESPAÑOL
Precauciones Importantes ..............20
Simbolos IEC .................................... 20
Precauciones Importantes................ 20
Introducción......................................23
Enunciado De Uso Idóneo................ 23
Para Qué Se Utilizan Los Sistemas
¿De Compresor-nebulizador?........... 23
¿Cómo Funciona Un
Compresor-nebulizador? .................. 23
¿Cómo Debo Administrar El
Tratamiento? ..................................... 23
Identificación De Producto
Y Accesorios disponibles ................25
Operarcion ........................................26
Cómo Operar Su Compresor............ 26
Limpieza Y Mantenimiento..............28
Limpieza Del Nebulizador ................. 28
Limpieza Del Compresor...................29
Cambio De Filtro............................... 29
Mantenimiento .................................. 29
Especificaciones ..............................30
Garantía Limitada.............................36
FRANÇAIS
Mises En Garde Importantes...........37
Symboles CEI ................................... 37
Mises En Garde Importantes ............ 37
Introduction.......................................40
Déclaration D’utilisation
Envisagée.......................................... 40
À Quels Usages Les Systèmes
De Nébuliseur à Compresseur
Sont–ils Destinés? ............................ 40
Comment Fonctionne Un
Nébuliseur?....................................... 40
Comment Dois-je Prendre Mon
Traitement? ....................................... 41
Identification Du Produit Et
Accessoires disponibles..................42
Utilisation ..........................................43
Comment Faire Fonctionner Le
Compresseu...................................... 43
Nettoyage Et Entretien.....................45
Nettoyage Du Nébuliseur.................. 45
Nettoyage Du Compresseur ............. 46
Changement Du Filtre....................... 46
Entretien............................................ 46
Caractéristiques ...............................47
Garantie Limitée ...............................53

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important safeguards
Alternating
Current
WEEE
Waste Electrical
and Electronic
Equipment
IP21— Protected against foreign objects equal
to greater than 12.5 mm in diameter and against
vertically falling drops of water
Rx only: Federal (U.S.) Law restricts this device
to sale by or on the order of a physician
Type BF
Applied Part
Class II
Equipment
Important Safeguards
When using electrical products, especially when children are present, basic safety precau-
tions should always be followed. Read all instructions before using. Important information is
highlighted by these terms:
DANGER Urgent safety information for hazards that will cause serious injury or death.
WARNING Important safety information for hazards that might cause serious injury.
CAUTION Information for preventing damage to the product.
NOTE Information to which you should pay special attention.
Read All Instructions Before Using
To reduce the risk of electrocution:
1. Always unplug this product immediately after using.
2. Do not use while bathing.
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.
WARNING: If any of the motor housing parts should become detached or broken ex-
posing the motor or any other electrical component operation should
be discontinued immediately to avoid personal injury or further product
damage.
To reduce the risk of burns, electrocution, fire or injury
to persons:
1. The product should never be left unattended when plugged in.
2. Close supervision is necessary when this product is used by, on, or near children
or disabled individuals
3. Use this product only for its intended use as described in this guide. Do not use
attachments not recommended by the manufacturer.
4. Never operate this product if:
a. It has a damaged power cord or plug. c. It has been dropped or damaged.
b. It is not working properly. d. It has been dropped into water.
5. Keep the power cord away from heated surfaces.
6. Never allow the power cord to be pulled, jerked, strained, twisted or severely bent
1
ON OFF
Attention, consult
instruction guide.
Refer to instruction
manual / booklet
DANGER!
WARNING!
IP 21

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important safeguards
DANGER!
WARNING!
especially at the plug connections. Damage will occur at the high ex point of entry
to the device, causing it to rupture and short.
7. Never block the air openings of the product or place it on a soft surface, such as
bed or couch, where the air openings may be blocked. Keep the air openings free of
lint, hair, and the like.
8. Never use while drowsy or asleep.
9. Never drop or insert any object into any opening or hose.
10. Do not use outdoors. This product is for household use only.
11. DO NOT use this product in or near explosive environments, or where aerosol (spray)
products are being used.
12. DO NOT pump combustible liquids or vapors with the product or use in or near an
area where ammable or explosive liquids or vapors may exist.
13. DO NOT operate this product in an oxygen enriched environment, i.e. oxygen tent
or oxygen hood.
14. Use only in well ventilated areas.
15. Do not use this product with a DC to AC converter, or with any AC voltage and/or
frequency other than specied.
16. Do not operate unit in a backpack or carrying bag.
17. Care should be taken when this product is used in the vicinity of other electronic
equipment concerning the possible interference between them. They may need to
be moved apart.
18. Use caution when plugging in and unplugging device. Do not allow jewelry or other
metal items to contact plug.
19. Warning: This product contains small parts that may represent a choking hazard.
20. The device does not need to be calibrated.
21. Do not position the equipment so that it is dicult to operate.
22. To avoid strangulation and entanglement, keep power cord and air tubes out of
reach of young children.
23. The air lter shall not be serviced or maintained while the compressor is in use.
24. Warning: No modication of this equipment is allowed.
NOTE This unit employs a temperature and/or current limiting device that will shut o the
entire product should a malfunction occur or in the event of product misuse, abuse, or abnor-
mal operation.
NOTE This is based on the thermal interrupt safety device that is integrated into the motor.
As the unit runs it generates heat and gets warm. If the unit is run for over 30 minutes con-
tinuously the thermal interrupt may trip which would stop the user’s treatment. Some models
of this appliance have a polarized plug (one blade is wider than the other). As a safety feature,
this plug will t in a polarized outlet only one way. If the plug does not t fully in the outlet,
reverse the plug. If it still does not t, contact a qualied electrician. Do not attempt to defeat
this safety feature. If repair or replacement of the cord or plug is necessary, contact your
qualied Drive provider.

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introduction
NOTE The exterior surfaces of the unit and the air outlet connector may become slightly
warm to the touch during use. Warm air can also be felt exiting the vents on the sides of the
case of the unit. This is normal.Your doctor has prescribed a liquid medication to treat your
respiratory condition. To best utilize this liquid medication, he has prescribed a Drive brand
compressor nebulizer. Your Drive compressor nebulizer works to convert the medication to
a high-quality mist of ne particles that penetrates deep into the lungs.
Be sure that you read and understand the information in this instruction guide. By following
these simple instructions and the advice of your physician, your compressor will become
an eective addition to your therapeutic routine.
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 specic drugs for inhalation by a
patient and requires the order of a physician for medical use.
What are Compressor Nebulizer Systems Used For?
People with breathing problems, such as Asthma, Chronic Obstructive Pulmonary Disease
(COPD) or Cystic Fibrosis are often prescribed medicines that minimize or control symp-
toms of their disease. Compressor Nebulizer Systems are a means of delivering these
prescribed medications to the lungs. These medications and the compressor nebulizer
systems should be used as directed by a physician to maximize benets. Compressor
Nebulizer systems can be prescribed for use everyday or periodically as symptoms present
themselves, such as the springtime when Hay Fever or Allergies are normally present.
How Does a Compressor Nebulizer Work?
Most medicines for use with a compressor nebulizer system are created in a liquid form.
This liquid medication is placed in the “cup” of the nebulizer (please refer to this Instruc-
tion Guide for more information on the proper use of a nebulizer). The compressor, which
is connected to the nebulizer by exible tubing, generates a specic pressure and ow of
air that essentially “drives” the nebulizer. The pressurized air produced by the compressor
initiates the nebulizer’s ability to break down the liquid medication into a very ne mist. This
mist, often referred to as an aerosol cloud, is then propelled out the nebulizer and inhaled
into the lungs where the medicine is readily absorbed. Please consult your prescription for
details on the amount of liquid medication that should be placed in the nebulizer. If you
should have any questions about your medication or its use, please contact your physician
or pharmacist.
2

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introduction
How Do I Take a Treatment?
A nebulizer is the optimal delivery method of medication to the lungs. However, some users
may nd it dicult to use, especially very young children. In this case, an aerosol mask
may be used. To ensure that the proper mask is utilized, please consult your home health
provider or physician.
The most important aspect of taking a treatment is the patient’s breathing pattern while
inhaling the medication mist.
It should be slow and deep, all attempts should be made to sit up straight and breathe in
deep.
A general rule of thumb is to attempt to breathe in so deeply that it feels as though the
lungs are completely full of air and inhaling any additional air is impossible.
If possible, hold your breath for 1-2 seconds unless directed otherwise by your physician
and then slowly exhale through the nebulizer mouthpiece or mask. Holding your breath for
1-2 seconds after inhaling the medication allows for optimal absorption of medication in the
lungs.
Repeat this breathing pattern for the entire treatment.
The length of a treatment can last anywhere from 5 to 20 minutes, depending on the
amount of medication and the performance of your compressor and nebulizer system.
When you cannot see any medication in the nebulizer cup and the nebulizer has stopped
producing a mist, the treatment has been completed. Turn o your compressor and follow
the cleaning instructions found in this instruction guide.
If you have any additional questions regarding your equipment, medication, or treatment,
please consult your physician.

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available accessories
Product Identification
MODELS DESCRIPTIONS
MQ5800 Compact Compressor Nebulizer with JetNeb Kit
MQ5900 Compact Compressor Nebulizer with JetNeb Kit and
Neb Kit 500
MQ5900P Compact Compressor Nebulizer with JetNeb Kit, Neb
Kit 500 and JetNeb Pediatric Mask
Available Accessories
18260 18260 JetNeb Kit with mouthpiece, tubing (12/cs)
NEB KIT 500 Disposable Nebulizer Kit with mouthpiece, 7’ tubing (50/cs)
MASK 001P Pediatric Aerosol Mask (50/cs)
MQ92692 Replacement Filter (5/bag)
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available accessories
How to Operate Your Compressor
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.
Daily Use Operation
CAUTION The Compressor is designed for intermittent use only. Do not
operate it continuously for more than 30 minutes for a single
use without turning it o and following a cooling period for
least 30 minutes.
1. Before each use inspect the Compressor and nebulizer cup assembly
for damage or wear, replace as needed.
2. Place the Compressor on a table or other at stable surface. Be sure
you can easily reach the controls when seated. Do not use this device on
the oor.
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-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 found at the
bottom of the nebulizer cup.
7. Turn on the 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 o the compressor by pressing the
power switch to O (OFF) position and unplug the unit from the electrical
outlet.
10. Always unplug this device immediately after use.
Equipment not suitable for use in the presence of a ammable anesthetic
mixture with air or with oxygen or nitrous oxide. This device has no AP or
APG protection not intended for use with oxygen or oxygen enriched
environments.
operation
4

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11. DO NOT use this product in or near explosive environments, or where aerosol
(spray) products are being used.
12. DO NOT pump combustible liquids or vapors with the product or use in or near an
area where ammable or explosive liquids or vapors may exist.
13. DO NOT operate this product in an oxygen enriched environment, i.e. oxygen tent
or oxygen hood.
14. Use only in well ventilated areas.
Safety Overload
NOTE Do not exceed 30 minutes of continuous operation.
NOTE This is based on the thermal interrupt safety device that is integrated into the mo-
tor. As the unit runs it generates heat and gets warm. The thermal interrupt will cut
power to the unit if the temperature inside gets to an unsafe level. Once the unit
cools o it will work normally. If the unit is run for over 30 minutes continuously the
thermal interrupt may trip which would stop the user’s treatment
1. The motor of this device has a built-in thermal overload protector. Should the mo-
tor overheat, the protector will automatically shut o 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 o the motor frequently, you may have an unstable
voltage situation.

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Nebulizer Cleaning (JetNeb Kit)
All parts of the nebulizer, except tubing, should be cleaned according to the following
instructions. Your physician and/or drug provider may specify a certain cleaning procedure.
If so, follow their recommendations.
WARNING: Clean nebulizer after each use. Risk of bacteria
growth, infection, illness from contamination due to dirty nebulizer.
Cleaning:
1. Ensure that the power cord is disconnected from the power outlet.
2. Disconnect nebulizer from tubing and compressor. Do not wash or
submerge the air tubing.
3. Disassemble all parts of nebulizer by twisting the top and bottom,
separating the pieces,
4. Clean nebulizer in warm soapy water.
5. Rinse all parts with clear water to remove any residue.
6. Allow the nebulizer and all parts to air dry completely and store in a clean plastic
bag or container.
The 18260 JetNeb Nebulizer is intended for single patient
use and should not be shared with other people. This unit
should be replaced every thirty days.
Use and Cleaning of NEBKIT 500: refer to the user manual of NEBKIT 500 which is included
in the accessory pack of NEBKIT 500 independently
Compressor Cleaning
1. With power switch in the “O” position, unplug power cord from wall outlet.
2. Wipe outside of the compressor cabinet with a clean damp cloth to
keep dust-free.
CAUTION: do not use any powdered cleaners or soap
pads which may damage the nish.
WARNING: Do not submerge the compressor in water;
doing so will result in compressor damage.
Filter Change
cleaning and maintenance
5
WARNING!
WARNING!
CAUTION
CAUTION

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Change lter every 30 days or when lter turns gray.
CAUTION: Never operate the unit without a lter.
Do not substitute cotton or any other
materials for the lters. Do not attempt to clean the
lters or reuse a lter.
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.
Maintenance
All maintenance must be performed by a qualied Drive provider or authorized
service center.
Electric shock hazard. Do not remove compressor cabinet.
All disassembly and maintenance must be done by a qualied
Drive provider.
Filter Cover
CAUTION
WARNING!

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CAUTION
WARNING!
Size 7.5 in X 3.7 in X 5.7 in
Weight 3.0 lbs
Operating Voltage 120VAC, single phase, 60Hz
Current Consumption 2A (Max)
Storage/Transport Temperature Range -13 to 158°F, (-25 to 70°C)
Storage/Transport Humidity 10 – 95%
Operating Humidity 10 – 95%
Operating Temperature Range 50 to 104°F, (10 to 40°C)
Compressor Flow Rate ≥9 L/minute
Operating Pressure Range 8~13 psi /55Kpa~90Kpa
Operating Noise Level 52 +\-5 dB(A)
Service Life 1080 hours
18260 JetNeb Nebulizer
Min & Max lling volume 2~8 ml
Particle size (MMAD) <5 µm
Nebulization rate ≥0.25 ml/min.
Disposable nebulizer 30 days
For specification of NEBKIT 500: refer to the user manual of NEBKIT 500, which is
included in the accessory pack of NEBKIT 500 independently.
Equipment Classifications:
Protection against electric shock: Class II
Degree of protection against electric shock: Type BF
Equipment not suitable for use in the presence of ammable anaesthetic mixture with air.
Not intended for use with oxygen enriched environments such as oxygen hoods or tents.
*Conditions may vary based on altitude above sea level,barometric pressure, and temperature.
**Value determined with minimum ow rate through the nebulizer (20°C, sea level).
There are no hazardous materials used in the construction of this unit, therefore, there are
no known risks associated with disposal of the equipment.
This product complies with the following electromagnetic compatibility standard:
IEC 60601-1-2
Please dispose of this nebulizer in accordance with local, municipal, state
and federal law for electronic devices
specications
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Particle size (MMAD) – tested with Cascade impactor for 18260
Features Drug Resul
Particle Size (MMAD) (μm)
Albuterol Sulfate (2.5 mg/3 ml) 3.40±0.44
Ipratropium Bromide (0.5 mg/2.5 ml) 2.87±0.0.21
Cromolyn Sodium (20 mg/2.0 ml) 3.43±0.81
Geometric Standard Deviation
Albuterol Sulfate (2.5 mg/3 ml) 3.07±0.35
Ipratropium Bromide (0.5 mg/2.5 ml) 3.38±0.23
Cromolyn Sodium (20 mg/2.0 ml) 3.74±0.97
Total Dose Delivered (μg)
Albuterol Sulfate (2.5 mg/3 ml) 759±62
Ipratropium Bromide (0.5 mg/2.5 ml) 161±13
Cromolyn Sodium (20 mg/2.0 ml) 3494±508
Total Respirable Dose (0.5-5 um) (μg)
Albuterol Sulfate (2.5 mg/3 ml) 343±24
Ipratropium Bromide (0.5 mg/2.5 ml) 72±9
Cromolyn Sodium (20 mg/2.0 ml) 1528±169
Coarse Particle Dose (>4.7 um) (μg)
Albuterol Sulfate (2.5 mg/3 ml) 390±49
Ipratropium Bromide (0.5 mg/2.5 ml) 77±11
Cromolyn Sodium (20 mg/2.0 ml) 1758±492
Fine Particle Dose (<4.7 um) (μg)
Albuterol Sulfate (2.5 mg/3 ml) 369±18
Ipratropium Bromide (0.5 mg/2.5 ml) 84±7
Cromolyn Sodium (20 mg/2.0 ml) 1736±168
Ultra-Fine Particle Dose (<1.0 um) (μg)
Albuterol Sulfate (2.5 mg/3 ml) 117±4
Ipratropium Bromide (0.5 mg/2.5 ml) 29±4
Cromolyn Sodium (20 mg/2.0 ml) 606±66
Recommended separation distances between portable and mobile RF
communications equipment and the Compressor Nebulizer.
The Compressor Nebulizer is intended for use in an electromagnetic environment in which
radiated RF disturbances are controlled. The customer or the user of the Compressor
Nebulizer can help prevent electromagnetic interference by maintaining a minimum dis-
tance between portable and mobile RF communications equipment (transmitters) and the
Compressor Nebulizer as recommended below, according to the maximum output power
of the communications equipment.

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Recommended separation distances between portable and mobile RF communications equipment and
the []
The Device is intended for use in an electromagnetic environment in which radiated RF disturbances are con-
trolled. The customer or the user of the Device can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the Device as
recommended below, according to the maximum output power of the communications equipment.
Rated maximum output
power of transmitter
W
Separation distance according to frequency of transmitter
m
150 kHz to 80
MHz (out ISM
and amateur
radio bands)
d = 1.2√p
150 kHz to 80
MHz (in ISM and
amateur radio
bands)
d = 2√p
80MHz to
800MHz
d = 1.2√p
800MHz to
2.7GHz
d = 2.3√p
0,01 0.12 0.2 0.12 0.23
0,1 0.38 0.632 0.38 0.73
11.2 21.2 2.3
10 3.8 6.32 3.8 7.3
100 12 20 12 23
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in
metres (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maxi-
mum 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 aected by absorption
and reection from structures, objects and people.
Guidance and manufacturer’s declaration - electromagnetic emissions
The Device is intended for use in the electromagnetic environment specied below. The customer or the user of
the Device should assure that 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 Includ- ing domestic and those directly connected to the public
low-voltage power supply network that supplies buildings
used for domestic purposes.
Harmonic emissions
IEC 61000-3-2 Class A
Voltage uctuations/
icker emissions
IEC 61000-3-3
Complies

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Guidance and manufacturer’s declaration - electromagnetic Immunity
The Device is intended for use in the electromagnetic environment specied below. The customer or the user of
the Device should assure that it is used in such an environment
Immunity Test IEC 60601
Test level
Compliance level Electromagnetic environment - gui-
dance
Electrostatic
discharge (ESD)
IEC 61000-4-2
±8 kV contact
±15 kV air ±8 kV contact ±15 kV air Floors should be wood, concrete or ceramic tile. If oors are covered with
synthetic material, the relative humidity
should be at least 30 %
Electrical fast tran-
sient/burst
IEC 61000-4-4
Power supply lines:
±2 kV
input/output lines:
±1 kV
Power supply lines:
±2 kV Mains power quality should be that of a typical commercial or hospital environ-
ment.
Surge
IEC 61000-4-5 line(s) to line(s): ±1 kV.
line(s) to earth:
±2 kV.
100 kHz repetition
frequency
line(s) to line(s): ±1 kV.
100 kHz repetition
frequency
Mains power quality should be that of a
typical commercial or hospital environ-
ment.
Voltage dips, short
interruptions and
voltage variations on
power supply input
lines
IEC 61000-4-11
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
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
Mains power quality should be that of a
typical commercial or hospital environ-
ment.
Power frequency
(50/60Hz)
magnetic eld
IEC 61000-4-8
30 A/m
50Hz/60Hz 30 A/m 50Hz/60Hz Power frequency magnetic elds should be at levels characteristic of a typical loca-
tion in a typical commercial or hospital
environment.
NOTE UT is the a.c. mains voltage prior to application of the test level.

.............................................................................................................................
DRIVE COMPRESSOR/NEBULIZER MODEL MQ5800, MQ5900, MQ5900P
.............................................................................................................................
17
Guidance and manufacturer’s declaration - electromagnetic Immunity
The Device is intended for use in the electromagnetic environment specied below. The customer or the user of
the Device should assure that it is used in such an environment
Immunity
Test
IEC 60601
Test level
Compliance
level
Electromagnetic environment - guidance
Conduced RF
IEC61000-4-6 150KHz to 80MHz:
3Vrms
6Vrms (in ISM
and amateur
radio bands)
80% Am at
1kHz
150KHz to
80MHz:
3Vrms
6Vrms (in ISM
and amateur
radio bands)
80% Am at 1kHz
Portable and mobile RF communications equipment should
be used no closer to any part of the Device ,including
cables, than the recommended separation distance calcu-
lated from the equation appropriate for the frequency of the
transmitter. Recommended separation
distances:
d = 1.2√P;
d = 2√P
Radiated RF
IEC61000-4-3 10V/m 10V/m 80MHz to 800MHz:
d=1.2
800MHz to
2.7 GHz:
d = 2.3√P
Where P is the maximum output power
rating of the transmitter in watts (W) ac-
cording to the transmitter manufacturer,
d is the recommended separation dis-
tance in meters (m) Field strengths from
xed RF transmitters, as determined by
an electromagnetic site surveya ,should
be less than the compliance level in each
frequency range b
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 aected by absorption
and reection from structures, objects and people.
a 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 the [XXXXX] is used exceeds
the applicable RF compliance level above, the [XXXXX] should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as re-orienting or relocating the [XXXXX].
b Over the frequency range 150 kHz to 80 MHz, eld strengths should be less than 3 V/m.

.............................................................................................................................
DRIVE COMPRESSOR/NEBULIZER MODEL MQ5800, MQ5900, MQ5900P
.............................................................................................................................
18
Guidance and manufacturer’s declaration - electromagnetic Immunity
The Device is intended for use in the electromagnetic environment specied below. The customer or the user of
the Device should assure that it is used in such an environment
Radiated RF
IEC61000-4-3
(Test specifica-
tions for
ENCLOSURE
PORT
IMMUNITY to
RF wireless
communications
equipment)
Test
Frequency
(MHz)
Band a)
(MHz)
Service a) Modulation b) Modulation b)
(W)
Distance
(m)
IMMUNITY
TEST LEVEL
(V/m)
385 380
–390
TETRA 400 Pulse
modulation b)
18 Hz
1,8 0,3 27
450 380
–390
GMRS 460,
FRS 460
FM c)
± 5 kHz devia-
tion
1 kHz sine
20,3 28
710 704 –
787
LTE Band 13,
17
Pulse
modulation b)
217 Hz
0,2 0,3 9
745
780
810 800 –
960
GSM 800/900,
TETRA 800,
iDEN 820,
CDMA 850,
LTE Band 5
Pulse
modulation b)
18 Hz
20,3 28
870
930
1720 1 700 –
1 990
GSM 1800;
CDMA 1900;
GSM 1900;
DECT;
LTE Band 1, 3,
4, 25; UMTS
Pulse
modulation b)
217 Hz
20,3 28
1845
1970
2450 2 400 –
2 570
Bluetooth,
WLAN,
802.11 b/g/n,
RFID 2450,
LTE Band 7
Pulse
modulation b)
217 Hz
20,3 28
5240 5 100 –
5 800
WLAN 802.11
a/n
Pulse
modulation b)
217 Hz
0,2 0,3 9
5240
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:
E=6/d √P
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.

.............................................................................................................................
DRIVE COMPRESSOR/NEBULIZER MODEL MQ5800, MQ5900, MQ5900P
.............................................................................................................................
19
Five-Year Limited Warranty on Compressor Parts
Your Drive brand product is warranted to be free of defects in materials and workmanship
for ve years of the original consumer purchaser.
This device was built to exacting standards and carefully inspected prior to shipment. This
5 year Limited Warranty is an expression of our condence in the materials and
workmanship of our products and our assurance to the consumer of years of dependable
service.
This warranty does not cover device failure due to owner misuse or negligence, or normal
wear and tear. The warranty does not extend to non-durable components which are
subject to normal wear and need periodic replacement.
If you have a question about your Drive device or this warranty, please contact an
authorized Drive dealer.
Save These Instructions
limited warranty
7

.............................................................................................................................
DRIVE COMPRESSOR/NEBULIZER MODEL MQ5800, MQ5900, MQ5900P
.............................................................................................................................
20
importantes medidas de seguridad
Encindido Apagaoo Atención, consulte
Medidas Importantes De Seguridad
Cuando use productos eléctricos, especialmente si los niños están presentes, siempre se
deben tomar precauciones de seguridad. Lea todas las instrucciones antes de usarlo. La
información importante está resaltada por estos términos:
PELIGR Información se seguridad urgente sobre peligros que pueden ocasionar
lesiones graves o la muerte.
ADVERTENCIA Información de seguridad importante sobre peligros que pueden
ocasionar lesiones graves.
PRECAUCIÓN Información para evitar dañar el producto.
NOTA Información a la que debe poner atención especial.
Lea Todas las Instrucciones Antes de Su Uso
Para reducir el riesgo de choque eléctrico:
1. Siempre desconecte este producto inmediatamente
después de usarlo.
2. No lo use mientras se está bañando.
3. No coloque o almacene el producto donde se pueda caer o jalar dentro de una
bañera o lavabo.
4. No lo coloque dentro o introduzca en agua u otro líquido.
5. No trate de sacar un producto que ha caído dentro del agua. Desconéctelo
inmediatamente.
ADVERTENCIA Si alguna de las partes de la carcasa del
motor debe desprenderse o roto la exposición de la de
cualquier otra operación componente eléctrico del motor o debería suspenderá de inmedi-
ato para evitar lesiones personales o daños mayores producto.
Para reducir el riesgo de quemaduras, descarga eléctrica, incendio o lesio-
nes a personas:
1. Nunca debe dejar el producto sin atender cuando esté conectado.
¡PELIGRO!
¡ADVERTENCIA!
1
Corriente
Alterna
WEEE
Residuos de
aparatos eléctricos
y electrónicos
IP21: Protección contra cuerpos extraños de un
diámetro igual o superior a 12.5 mm y contra la
caída de gotas de agua en forma vertical
Por prescripción médica únicamente: La ley
federal (EE. UU.) restringe la venta de este dis-
positivo a médicos o por prescripción facultativa
Tipo BF
Parte
Aplicada
Equipo de
Clase II
Encindido Apagaoo
Atención, consulte Consulte el
manual de
instrucciones /
folleto
IP 21