Respirox ASU-200 User manual

Aug. 10, 2017
"RESPİROX" Suction Unit

"RESPİROX" Suction Unit
ASU-200 User Manual

Contents
１、 Introduction ---------------------------------------------------------------- 2
２、 Product Description --------------------------------------------------------2
３、 Set-up ----------------------------------------------------------------------- 3
４、 Operation Instruction-------------------------------------------------------3
５、 Cleaning Maintain -------------------------------------------------------4
６、 Troubleshooting ------------------------------------------------------------4
７、 Technical Specification -----------------------------------------------------5
８、 Power Adapter---------------------------------------------------------------5
９、 Symbol Definitions ---------------------------------------------------------6
１０、Electromagnetic Compatibility---------------------------------------------7

Please read the instruction manual before use
Warning & Caution
1. This device is intended for use by professional. The manufacture recommends that
user train on use this device.
2. Do not place or store product where it can fall or be pulled into a tub or sink.
3. Do not place in or drop into water or other liquid.
4. Do not reach for a product that has fallen into water. Unplu immediately.
5. To reduce the risk of burns, electrocution, fire or injury.
6. This product should never be left unattended when plu ed in.
7. Close supervision is necessary when this product is used by, on, or near children or
invalids.
8. Use this product only for its intended use as described in this manual, do not use
attachments not recommended by the manufacturer.
9. Never operate this product if it has a dama ed cord or plu , if it is not workin
properly, if it has been dropped or dama ed, or dropped into water. Return the
product to the provider for examination and repair.
10. Keep the cord away from heated surfaces.
11. The device can also use for field and/or transport.
1

Cha ter 1. Introduction
1.1 General Information
Intend Use
The device is used to remove fluids from the airway or respiratory support system and infectious
materials from wounds. The device creates a ne ative pressure (vacuum) that draws fluids
throu h disposable tubin that is connected to a collection container. The fluids are trapped in
the collection container for proper disposal. It is for use on the order of a physician only.
THIS DEVICE IS NOT INTENDED FOR HEMOSPASIA
Cha ter 2. Product Descri tion
Product Standard Accessory
(1) Suction unit √
(2) Suction container √
(3) Connection tube √
(4) Bacteria filter
(5) Suction tube
(6) Remote controller
(7) Battery
(8) Power a apter √
(9) Carrying bag √
2

Cha ter 3. Set-u
(1) Connect the connection tube on the vacuum outlet.
(2) Connect the other side of connection tube on the suction container.
(3) Hook up the container with the container connection base.
(4) Connect either end of the suction tubin to the tubin connector then connect the other end to the
bacteria filter. Ensure that the clear side of the bacteria filter is toward elbow and container when
installin /re-installin . Do not reverse direction of filter
(5) Please assure that all connections are secure and without leaks before usin .
Cha ter 4. O eration Instruction
Front Panel
Device O eration
(1) Open the device.
(2) Adjust the pressure.
(3) Verify that unit is at desired suction level before be innin .
(4) Insert the suction tube to a suitable depth in patient’s nostril patient suction
(5) Close the device after use
Do Not Exceed 15 Seconds for Each Thera y
Do Not Block the Exhaust Outlet During Use
No Modification of this Equi ment is Allowed
To Avoid the Risk of Electric Shock, this Equi ment Must only be Connected to a Su ly Mains with
Protective Earth
If the rotect mechanism of the container triggered, turn off the device and disconnect the container
immediately.
3

Cha ter 5. Cleaning & Maintain
(1) Recommend that pour the liquid in the container before met the full line.
(2) Disinfected with diluted medical alcohol to clean the device surface after use.
(3) Disinfected with diluted medical alcohol to clean the accessories, such as suction container, connection
tube, and suction tube…etc.
(4) Char e the device for 3hrs at least once per month.
Cha ter 6. Troubleshooting
Problem Possible Cause Solutions
Pump runs,
but no vacuum
1. Tubin isn’t connected properly.
2. Tubin breaks or leaks.
3. Container do not assembly properly.
4. Container breaks or leaks.
1. Assembly the tube properly.
2. Contact your equipment provider
for repair
Unit does not
workin when
power is opened
1. Switch broken.
2. PCB board broken.
Contact your equipment provider for
repair
Vacuum
delivered, but
au e did not
display the
values
1. Tubin isn’t connected properly.
2. Gau e broken
Contact your equipment provider for
repair
Battery will not
hold a char e.
1. Char in IC broken
2. Battery life expires
1. Ensure that unit is equipped with
battery.
2. Verify that char e li ht turns on.
3. Check electrical connections
durin char in .
4. Contact your equipment provider
for repair
Low vacuum 1. Tubin isn’t connected properly.
2. Pump broken.
3. Suction container full.
1. Assembly the tube properly.
2. Contact your
equipment provider for repair
Abnormal sound
when the device
workin
1. Pump broken
2. Waste liquid or water countercurrent to
the machine
Contact your equipment provider for
repair
4

Cha ter 7. Technical S ecification
Item S ecifications
Power Consumption 35VA
Max Suction Pressure -600 mmH (-80 Kpa)
Exhaust Air Volume 24 L/MIN
Supply Volta e
AC 100-240V, 50/60Hz / DC 18V, 3.34A
Car Char er for DC 12V
Lithium Battery 14.8 VDC, 2.5 AH
Char in time: 3 hours
Usin Time: 60 min, after full char ed
Sound Level <70 dB (A)
Container 1000ml
Unit 190mm(L) x 110mm (W) x 175mm (H)
Wei ht 1.7 K
Temperature Operation: +10~+40˚C
Transport and Stora e: -15~+50˚C
Humidity 10％～90％RH
Operation Pressure 700-1060hPa
Operation Hei ht <3000m
Tube φ6mm* 1φ0mm*1800mm
Output level Hi h vacuum/Hi h flow
NOTE: The manufacturer reserves the right to modify the s ecification without notice
Cha ter 8. Power Ada ter
Part Number Descri tion UOM Manufacturer
UE60-
180334SPAX
AC Power
Cord for
ASU-200
1/ea Don uan Shilon Fuhua Electronic Co.,
Ltd.
The ower ada ter lug is also served to disconnect the device, not to osition the equi ment to make it
difficult to o erate the disconnection device.
5

Cha ter 9. Symbol Definitions
Symbol Ex lain Symbol Ex lain
Type BF applied part
The patient tubin is
applied part. IP21
Protect a ainst solid forei n objects of 50
mm & Protected a ainst vertically φ
fallin water drops
Attention, Consult
accompanyin
documents SN
Serial number of the product
Manufacturer Consult accompanyin documents
Manufacturin Date Authorized representative in the
European Community.
Dispose the waste
equipment accordin
to the national law.
6

Cha ter 10. Electromagnetic Com atibility
7

8

9

6F.-3, No.24, Wuquan 2nd Rd., Xinzhuang Dist.,
New Taipei City 242 Taiwan
IMPORTER :
Ece Tıbbi Cihazlar ve Medikal San.Tic.A.Ş
Mail : [email protected]
Website : www.ecemedikal.net
Telephone : [phone]
Turkey
Sümer Mh. 1782/17 The İstanbul Evleri Prof. Dr. Turan Güneş C
No:57/Ac ZEYTİNBURNUİSTANBUL d.