True Source TS-S0X Manual de usuario
TRUE SOURCE
User Manual
Air Pump
Model：TS-S0X (E2)
(X=0-9,A-Z)
UM-S0X-EN V1.1
Date: 20201015 Copyright by TRUE SOURCE Technology Co., Ltd.
2
Table of Contents
1. Safety Criteria/ Label content template
3
2. Warnings
5
3. Product Setup Contents
7
4. Product Features
8
5. Product description
9
6. Installation
10
7. Operating Principle
11
8. Air Pump Settings Contents
11
9. Routine Maintenance and Cleaning
13
10. Storage
13
11. Troubleshooting
14
12. Technical Specifications
16
13. EMC table
17
14. Warranty
23
15. Warranty Card
24
16. Contact
25
3
1. Safety Criteria
CE Marking
ISO 15223-1:2016 Ref no: 5.7.7 Medical Device
ISO 15223-1:2016 Ref no: 5.1.1 Manufacturer
ISO/DIS 20417 2019 Section 3.26 Single Patient -
multiple use
ISO 15223-1:2016 Ref no: 5.2.8 Do not use if
package is damaged
ISO 15223-1:2016 Ref no: 5.1.3 Date of
manufacture
ISO 7010-W012： Warning, electricity
ISO 15223-1:2016 Ref no: 5.1.7 Serial number
ISO 15223-1:2016 Ref no: 5.1.6 Catalogue number
ISO 15223-1:2016 Ref no: 5.1.9 Distributor
ISO 15223-1:2016 Ref no: 5.1.2 Authorized
representative in the European Community
ISO 15223-1:2016 Ref no:5.7.10 Unique Device
Identifier
ISO 15223-1:2016 Ref no: 5.2.7 Non-sterile
IEC 60417-5333： TYPE BF APPLIED PART
ISO 15223-1:2016 Ref no:5.3.7 Temperature
limitation
IEC 60417-5172： Class II Equipment
ISO 7000-0434A： Caution
4
ISO 7010-M002： Follow Instructions for Use
EN 50419 - Marking of electrical and electronic
equipment in accordance with article 11(2) of
Directive 2002/96/EC Separate collection for
waste of electrical and electronic equipment.
IEC 60417-5008： “OFF” (power)
IEC 60417-5007： “ON” (power)
No AP/APG
Non-applicable to the presence of flammable
anesthetics or a high concentration of oxygen in the
environment (AP or APG).
IP21
IEC 60529： Protected against solid foreign objects
of 12.5 mm ∅ and greater; Protection against
vertically falling water drops.
Label content template
Located at back of the air pump
5
2. Warnings
The product is only to be used as an auxiliary device. The
manufacturer does not have the absolute responsibility and
obligation to guarantee its full effects.
◼Intended Use: For purpose of aiding the prevention of pressure
ulcers and effective treatment of patients.
◼The air pump only use with the air mattress that manufacturer
provide together.
◼This Air pump for medical equipment used.
◼This Air pump is Continuous Operation.
◼Do not modify this equipment without authorization of the
manufacturer.
◼Users to be considered:
A) Installation personnel – only by manufacturer trained and
authorized technician for both device and mattress
B) Cleaning personnel – by professional healthcare personnel,
general personnel or lay user
C) Maintenance/repair personnel – only by manufacturer
trained and authorize technician
D) Operating personnel – Professional healthcare personnel,
general personnel or lay user which matches the user profile.
◼The equipment is intended for infant or adults by professional
healthcare personnel, general personnel or lay user which
matches the user profile.
◼The patient may also be an intended operator.
◼Please contact the manufacturer and local authorities if any
serious incident has occurred.
◼When getting severe back pain or feeling sick please consult
healthcare profession and stop using this device.
6
◼If there is any problem in setting up, using, maintaining, or to
report unexpected operation or events, please contact the
manufacturer or local distributor, do not try to repair the
defective equipment.
◼Potential allergic reactive may occur due to material sensitivity,
do not lie on the mattress directly with no clothes on.
◼Keep away from children, pests or pests when not using the
equipment.
◼Strangulation may be occurred due to excessive length of the
power cord or the air tube, please place the cord and tubing
where it can be easily disconnected and where unlikely to be in
contact with children or pets.
◼The age of the expected object is 20-60 years old, and the
expected load is defined according to different mattress types,
and the expected maximum is 250Kg.
◼When you need to dispose of your products, please follow the
guidance of your local authority or follow national
requirements.
◼This medical device can be used in home use environment and
professional healthcare.
Caution:
Do not open the Air Pump without guidance to prevent danger.
Do not insert items into any opening of the Air Pump.
Do not drop the Air Pump.
Do not use the Air Pump in places exposed to water, liquids, oil,
smoke, and flammable chemicals.
Use fuses as marked: T1A / 250V.
The device doesn’t be used in the presence of flammable The
device doesn’t be used in the presence of flammable
anesthetics mixture with air, oxygen or nitrous oxide
environment (No AP/APG).
7
Use a power cord that matches the voltage of the power outlet,
which has been approved and complies with the safety
standard of your particular country.
To prevent the risk of electric shock, make sure power cord is
unplugged from wall socket. To fully disengage the power to the
unit, please disconnect the power cord from the AC outlet.
The AC outlet shall be readily available and accessible.
For plug-in equipment, the power outlet socket must be located
near the equipment and must be easily accessible.
Turn off the power switch on the side panel and unplug the
power cord to ensure complete and safe shutdown of the
device.
3. Product Setup Contents
8
4. Product Features
Enhanced Design Features of the Air Pump
1. Air Pump integrated MPU is a “digital control system” that has
multiple smart options.
2. For hanging, the safest iron material is used for hanging hooks
and its withstanding ability is far higher than plastic material.
3. For shock absorption, the deflation pump inside is equipped
with a specially designed suspension shock absorption system
and a foot mat is provided outside the unit in order to reduce
the shock.
4. The compact size feature: The system is of a compact size,
making it easy for placement and storage and taking into
account the streamlined system appearance and practicality.
5. The cotton air filter is to be replaced outside. Therefore, the
replacement can be done without opening the unit.
6. Double external fuse holders allow the unit to provide better
safety protection.
7. The specialized power management with an independent
power cord and a master power switch on the side can better
ensure safety.
9
5. Product description
1. Control Panel 2. Knob 3.Front Case 4. Air Outlet (Quick
Coupling) 5. AC Inlet 6. Off/On Power Switch 7. Rear Case
A. Bed Hooks B. Fuses (T1A/250V) C. Label D. Air Filter
10
6. Installation
Step 1: Hang the Air Pump on the hospital bed at the feet end.
Step 2: Connect the hose at the feet end of the mattress to the air
outlet of the Air Pump.
Step 3: Connector the power cord to the AC Inlet of the Air Pump.
Step 4: Plug the power cord of the Air Pump to a socket with power
supply.
Step 5: Turn “ON” the power switch on the side of the Air Pump, and
the green indicator turns on. Air starts to enter the hose in a
few seconds.
Step 6: Weight setting Range “Knob” select comfort setting 1 to 10,
See” Air Pump Settings Contents”
Step 7: Please wait until all the air cells are inflated by at least 2/3 of
their volume (approx. 10mmHg) or for 30 minutes before the
user is allowed to lie on the mattress.
Note: Ensure that the patient does not bottom out.
◎Power-off procedure: Turn off the side power switch first, and
then unplug the power plug.
Tabla de contenidos
Otros manuales de Bomba de agua de True Source
Manuales populares de Bomba de agua de otras marcas
Sykes AmeriPumps
Sykes AmeriPumps GP100M Guía de solución de problemas
DUROMAX
DUROMAX XP WX Series Manual de usuario
BRINKMANN PUMPS
BRINKMANN PUMPS SBF550 Manual de usuario
Franklin Electric
Franklin Electric IPS Manual de usuario
Xylem
Xylem e-1532 Series Manual de usuario
Milton Roy
Milton Roy PRIMEROYAL Manual de usuario