A&D UN-019 User manual

Compressor Nebulizer
Model UN-019
Instruction Manual
Original
Manuel dinstructions
Traduction
Manual de Instrucciones
Traducción
Manuale di Istruzioni
Traduzione
Bedienungsanleitung
Übersetzung
1WMPD4004706

English 1
1. DEAR CUSTOMERS .................................................................. Page 2
2. PRELIMINARY REMARKS ......................................................... Page 2
3. SYMBOLS ................................................................................... Page 2
4. IMPORTANT SAFEGUARDS ..................................................... Page 3
5. INTRODUCTION ......................................................................... Page 5
6. SPECIFICATIONS ...................................................................... Page 5
7. PARTS IDENTIFICATION ........................................................... Page 6
8. OPERATING INSTRUCTIONS ................................................... Page 7
9. CLEANING .................................................................................. Page 8
10. MAINTENANCE .......................................................................... Page 8
11. TROUBLESHOOTING ................................................................ Page 9
12. TECHNICAL DATA .................................................................... Page 10
13. EMD TECHNICAL DATA ........................................................... Page 10
14. CORRECT DISPOSAL OF THIS PRODUCT
(WASTE ELECTRICAL & ELECTRONIC EQUIPMENT) ............. Page 13
CONTENTS

English 2
1. DEAR CUSTOMERS
Thank you for purchasing the UN-019 Compressor Nebulizer.
This device is a compact medical device designed to deliver the medication
prescribed by your doctor.
The compressor creates a stream of air that travels through the clear tubing to
the nebulizer which generates a mist of medicinal particles small enough to
reach the furthest parts of your lungs to provide maximum benefit for the
treatment of asthma, allergies and other respiratory disorders.
This device should be used only as directed. Do not use this device for
anything other than as prescribed by your doctor.
Before use, read this instruction manual thoroughly.
2. PRELIMINARY REMARKS
This device conforms to the European Directive 93/42 EEC for Medical
Products. This is proved the CE conformity marking CE1639. (1639: The
identification number of the Notified Body.)
3. SYMBOLS
Symbols Meaning
Caution Attention or Consult accompanying documents
Type BF Equipment
Alternating Current
Double Insulation
Indoor use only
Manufacturer
Refer to instruction manual
WEEE label
EU-representative
1639
EC directive medical device label

English 3
4. IMPORTANT SAFEGUARDS
CAUTION:
1. Federal Law restricts the sale or use of this device to an order by a physician.
2. Follow the instructions of your physician when operating this device.
3. This device is a nebulizer for the inhalation of medical aerosols and is
suitable for solutions used by children. Use only the type and amount of
medication prescribed by the patients doctor.
4. This device is intended for aerosol therapy only. Any other use is not
recommended.
5. Do not twist the air tube during operation.
6. Do not pour more than 6ml of solution into the device.
DANGER: Risk of electrocution.
7. Always disconnect the power cord from the electrical outlet immediately after
using.
8. Do not use while bathing.
9. Do not place or store the unit where it can fall or be pulled into a tub or
sink.
10. Do not place or drop the device into water or other liquid.
11. Do not reach for a product that has fallen into water. Disconnect the power cord
from the electrical outlet immediately.

English 4
WARNING: Risk of burns, electrocution, fire or injury
1. Electrical Shock Hazard: Do not remove the cabinet or open the cover.
2. Disconnect the power cord from the electrical outlet before cleaning or
servicing.
3. Do not place this device near hot, sparking or burning objects.
4. Do not use oil or grease on or near this device.
5. Turn the unit off when it is not in use.
6. Keep the cord away from HEATED or HOT surfaces.
7. NEVER drop or insert any object into any opening.
8. NEVER block the air openings of the product or place it on a soft surface,
such as a bed or couch, where the air openings may be blocked.
9. Avoid operating in wet or damp locations.
10. Disconnect the power cord from the electrical outlet before filling the
nebulizer cup.
11. When using this device near TVs, microwave ovens, pulse telephones, X-
rays, or other strong electric field, there may be electrical interference. It is
recommended to be far away from these devices when using this device.
WARNING: Risk of infection
1. This device is intended for both adult and pediatric patient use.
2. Cleaning of the device is recommended after each aerosol treatment.
Disinfecting is recommended once a day. Please follow cleaning and
disinfecting instructions in this manual.
This device is not suitable for use in anesthetics breathing systems.
This device is not suitable for solutions in suspension or high viscosity
liquids. In such cases information should be sought from the drug supplier.

English 5
5. INTRODUCTION
This compressor nebulizer is designed to deliver a prescribed medication
solution to treat patient respiratory disorders, such as asthma, allergies and
bronchitis. The device converts the medication solution into an aerosolized
mist which is inhaled by the patient through the mouthpiece or nosepiece or
mask. Read this manual thoroughly before using the device and store it for
future reference.
6. SPECIFICATIONS
Electrical Requirements 230 V / 50 Hz
Power Consumption Below 60 W
Rated Current Below 0.70 A
Dimensions Length 250mm × Width 118mm ×
Height 175mm
Weight 1.4kg(3.09lbs)
Sound Pressure Level 55 dBA
Max. Compression Pressure 35 psi to 50 psi (241 kPa to 345 kPa)
Neb. Operating Pressure 9-16 psi (62 kPa to 110 kPa)
Liter Flow Range 5-8 L/min
Average Nebulization Rate: Approx. 0.33 ml/min (6 ml medicine
can be nebulized within 18 minutes)
Maximum nebulizer solution capacity 6 ml
Maximum residual medicine volume 0.5 ml
Particle size (MMAD) Approximately 3 m
Operating Temperature/Humidity +10°C to + 40°C, 30% RH to 85% RH
Storage/Transport Temperature
Range/ Humidity - 20°C to + 70°C, 10% RH to 95% RH
Operating and Storage/Transport
Atmospheric Pressure 700 hPa to 1,060 hPa
Protection against electric shock
- Classified as Type
- Type BF applied parts: Mouthpiece, nosepiece, masks
Degree of safety in the presence of flammable anesthetics or oxygen 
No AP/APG (not suitable for use in the presence of flammable anesthetics or
oxygen)
Mode of operation  Continuous
IP21  Protection against harmful ingress of water is Ordinary.

English 6
7. PARTS IDENTIFICATION
1. Main unit
2. Adult mask
3. Child mask
4. Mouthpiece
5. Nosepiece
6. Air tube
7. Nebulizer cup
8. Air filters
9. Instruction manual
10. Carrying pouch
(Plug shape) C-plug: UN-019A-EC1B, BF-plug: UN-019A-EC2B
Replacement parts list
Appearance Part name Part code Qty Material
Adult mask UNB-014A-01EC 1 PVC
Child mask UNB-014A-02EC 1 PVC
Air tube UNB-014A-03EC 1 PVC
Air filter UNB-014A-04EC 5 urethane sponge
Nebulizer cup UNB-014A-05EC 1 PP, SAN
Mouthpiece
Nosepiece
UNB-014A-11EC 1 PP
Power switch
(" ":ON, " ":OFF)
Filter cover
Air outlet connector
1 2 3 4
5 6 7
8 9 10

English 7
8. OPERATING INSTRUCTIONS
1. Place the device on a stable, sturdy and flat surface so that the device
can be easily reached when you are seated.
2. Make sure that the device is in the "Off" (O) position by pressing on the
upper side of switch.
3. Plug power cord into a wall outlet.
4. Connect one end of the air tube into the air outlet connector on the device.
5. Add the prescribed solution through the opening on the cup using an eye
dropper or pre-measured dose container.
The "6cc" marking on the nebulizer cup is the maximum level.
Medication cannot be filled beyond the maximum level.
6. Insert the mouthpiece into the top of the nebulizer cup.
If nosepiece is used, insert it into the mouthpiece.
If a mask is used, connect the bottom of the mask to the top of the
nebulizer cup.
7. Connect another end of the air tube to nebulizer air inlet connector on the
bottom of the nebulizer cup.
8. Turn the power on to start the unit.
9. Initiate the treatment by placing the mouthpiece between the teeth.
Inhale through the mouthpiece and exhale through your nose.
If nosepiece is used, inhale through the nosepiece and exhale your mouth.
10. If a mask is used, place the mask over the mouth and nose.

English 8
9. CLEANING
1. Turn the power off and unplug from the wall outlet.
2. Remove the air tube from the air inlet connectors.
3. TO CLEAN: Remove the mouthpiece, nosepiece, mask, and disassemble the
nebulizer cup (cup, cap, and baffle), and wash these items in hot water with
dish-washing detergent. Rinse these items thoroughly to remove the detergent
and air dry.
4. TO DISINFECT: Mix one part of white vinegar with 3 parts hot water in a
clean container. Submerge mouthpiece, nosepiece, mask, and parts of
nebulizer cup for half an hour in the solution. Remove from solution and let
air dry.
5. There is no need to clean the tube. If necessary wipe the surface regularly.
Note:
Replace the nebulizer accessories including adult mask, child mask,
mouthpiece, nosepiece, nebulizer cup, Air tube after using 6 months.
Replace the filter every 30 days or if the filter turns grey.
CAUTION: The device must be changed if it becomes clogged.
CAUTION: The device and accessories must not be boiled.
10. MAINTENANCE
1. The air filter should be replaced when it turns gray. Additional filters can be
procured from your dealer.
2. Only authorized personnel shall make repairs to this device.
CAUTION: The device may be damaged if used with a dirty filter or if
the air filter is replaced by some other material such as
cotton. Do NOT operate without the dedicated air filter.

English 9
11. TROUBLESHOOTING
Check the following if the device should fail during operation. You can also
refer to the pages of this manual for complete instructions.
Problem Cause Remed
y
Nothing happens
when the power
switch is pressed.
The power cord is not
connected correctly to the
electrical outlet.
Check that the plug is inserted in
an electrical outlet. Unplug then
reinsert the plug if necessary.
No nebulization or
low nebulization
rate when the
power is on.
There is no medication in
the nebulizer cup.
Add the correct amount of
medication to the nebulizer
cup.
There is too much/little
medication in the nebulizer
cup.
The cap of nebulizer cup is
missing or not assembled
correctly.
Attach the cap of nebulizer cup
correctly.
The accessory for inhale is
not assembled correctly.
Assemble the accessory for
inhale correctly.
The nozzle of nebulizer cup
is blocked.
Make sure that the nozzle is free
of blockages.
The nebulizer cup is tilted
at a sharp angle.
Make sure that the nebulizer kit
is not tilted at an angle of more
than 45 degrees.
The air tube is not
connected correctly.
Make sure that the air tube is
correctly connected to the
compressor and accessory
for inhale.
The air tube is folded or
damaged.
Make sure that the air tube does
not contain kinks.
The air tube is blocked. Make sure that the air tube is
free of blockages.
The air filter is dirty. Replace the air filter with a new
one.
The device is
abnormally loud.
The air filter cover is not
attached correctly.
Attach the air filter cover
correctly.
The device is very
hot.
The device is covered by
something.
Do not cover the device with
any type of cover during use.
The device was operated
continuously for over 20
minutes.
Limit use to 20 minutes at a
time, and allow a 40 minute rest
interval before using the device
again.
NOTE: If the suggested remedy does not solve the problem, do not try
to repair the device. No parts of the unit are user serviceable.
Return the unit to an authorized retail outlet or distributor.

English 10
12. TECHNICAL DATA
Particle Size: **MMAD * approximately 3 um
Appropriate Medication Quantities: 2 ml minimum  6 ml maximum
Nebulization rate: 0.33 ml/min (by weight loss)
Aerosol Output: **0.33 ml (2 ml, 1%NaF)
Aerosol Output Rate: **0.06 ml/min (2ml, 1%NaF)
Result of cascade impactor **measurements for particle size
MMAD = Mass Median Aerodynamic Diameter
13. EMD TECHNICAL DATA
Medical Electrical Equipment needs special precautions regarding EMD and needs
to be installed and put into service according to the EMD information provided in
the following.
Portable and mobile RF communication equipment (e.g. cell phones) can affect
Medical Electrical Equipment. The use of accessories and cables other than those
specified may result in increased emissions or decreased immunity of the unit.

English 11
Table 1 - EMISSION Limits -
Phenomenon Compliance
Conducted and radiated RF EMISSION CISPR 11 Group 1 Class B
Harmonic distortion IEC 61000-3-2 Class A
Voltage fluctuations and flicker IEC 61000-3-3 Compliance
Table 2 - IMMUNITY TEST LEVELS : Enclosure Port -
Phenomenon IMMUNITY TEST LEVELS
Electrostatic discharge
IEC 61000-4-2
±8 kV contact
±2 kV, ±4 kV, ±8 kV, ±15 kV air
Radiated RF EM fields
IEC 61000-4-3
10 V/m
80 MHz - 2.7 GHz
80 % AM at 1 kHz
Proximity fields from RF wireless communications
equipment IEC 61000-4-3 See table 4
Rated power frequency magnetic fields
IEC 61000-4-8
30 A/m
50 Hz or 60 Hz
Table 3 - IMMUNITY TEST LEVELS : Input a.c. power Port -
Phenomenon IMMUNITY TEST LEVELS
Electrical fast transients / bursts
IEC 61000-4-4
±2 kV
100 kHz repetition frequency
Surges Line-to-line IEC 61000-4-5 ±0.5 kV, ±1 kV
Conducted disturbances induced by
RF fields IEC 61000-4-6
3 V 0.15 MHz - 80 MHz
6 V in ISM and amateur radio bands between 0.15
MHz and 80 MHz 80 % AM at 1 kHz
Voltage dips IEC 61000-4-11
0 % UT; 0.5 cycle
At 0°, 45°, 90°, 135°, 180°, 225°, 270°, and 315°
0 % UT; 1 cycle And 70 % UT; 25/30 cycle
Single phase: at 0°
Voltage interruption IEC 61000-4-11 0% UT; 250/300 cycle
NOTE UT is the AC mains voltage prior to application of the test level.

English 12
Table 4 - Test specifications for ENCLOSURE PORT IMMUNITY to RF wireless
communications equipment -
Test
frequency
(MHz)
Band
(MHz) Service Modulation
Maximum
power
(W)
Distance
(m)
IMMUNITY
TEST
LEVEL
(V/m)
385 380 - 390 TETRA 400
Pulse
modulation
18 Hz
1.8 0.3 27
450 430 - 470 GMRS 460
FRS 460
FM
±5 kHz
deviation
1 kHz sine
2 0.3 28
710
704 - 787 LTE Band 13,17
Pulse
modulation
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
18 Hz
2 0.3 28 870
930
1720
1700 -1990
GSM 1800
CDMA 1900
GSM 1900
DECT
LTE Band 1,3,4,25
UMTS
Pulse
modulation
217 Hz
2 0.3 28 1845
1970
2450 2400 - 2570
Bluetooth
WLAN 802.11 b/g/n
RFID 2450
LTE Band 7
Pulse
modulation
217 Hz
2 0.3 28
5240
5100 - 5800 WLAN 802.11 a/n
Pulse
modulation
217 Hz
0.2 0.3 9 5500
5785

English 13
14. CORRECT DISPOSAL OF THIS PRODUCT
(WASTE ELECTRICAL & ELECTRONIC EQUIPMENT)
This marking shown on this product and its literature, indicates that it
should not be disposed of with other household wastes at the end of its
working life. To prevent possible harm to the environment or human health
from uncontrolled waste disposal, please separate this from other types of
wastes and recycle it responsibly to promote the sustainable reuse of
material resources.
Household users should contact either the retailer where they purchased this
product, or their local government office for details of where and how they
can dispose this item for environmentally safe recycling.
This device does not contain any hazardous substances.

English 14
MEMO

A
&D Company, Ltd.
1-243 Asahi , Kitamoto-shi, Saitama 364-8585, JAPAN
Telephone: [81] (48) 593-1111 Fax: [81] (48) 593-1119
Shenzhen Bi-rich Medical Devices Co.Ltd,
The 1st Building of No. 10, Xinqiao GangZai Road, Xinqiao Street, Bao'An District ,518125,
Shenzhen City,Guangdong Province, P. R. China
SUNGO Cert GmbH
Lindenstraße 48-52, 40233 Dusseldorf, Germany
A&D INSTRUMENTS LIMITED
Unit 24/26 Blacklands Way, Abingdon Business Park, Abingdon, Oxfordshire OX14
1DY United Kingdom
Telephone: [44] (1235) 550420 Fax: [44] (1235) 550485
A&D ENGINEERING, INC.
4622 Runway Boulevard, Ann Arbor, MI 48108 USA
Telephone: [1] [phone]
A&D AUSTRALASIA PTY LTD
32 Dew Street, Thebarton, South Australia 5031, AUSTRALIA
Telephone: [61] (8) 8301-8100 Fax: [61] (8) 8352-7409
OOO A&D RUS OOO " "
121357, , . , . , 17
( Business-Center "Vereyskaya Plaza-2" 121357, Russian Federation, Moscow,
Vereyskaya Street 17 )
.: [7] [phone] : [7] [phone]
A&D Technology Trading(Shanghai) Co. Ltd
855 32 C,D 200120
(32CD, World Plaza, No.855 South Pudong Road,China (Shanghai) Pilot
Free Trade Zone, 200120, China)
: [86] (21) 3393-2340 : [86] (21) 3393-2347
A&D INSTRUMENTS INDIA PRIVATE LIMITED
( 509, Udyog Vihar, Phase- , Gurgaon - 122 016, Haryana, India )
: 91-124-4715555 : 91-124-4715599
1639