True Source TS-S0X User manual

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.

11
7. Operating Principle
This is an air pump using air compressor to fill up the pressure air
mattress.
It is an air pump delivers air through air outlet to pressure air
mattress by an air compressor which auto detects pressure by
control PCB and stops/re-fills the pressure when deemed necessary.
Description
Use air pump to inflate or deflate the air cells, which can regularly
and automatically change the distribution of body pressure.
8. Air Pump Settings Contents
(Representative Model: TS-S00)
Button Function Area
(1) Comfort Knob:
Select a setting according to the patient’s weight . Knob numbers
from left to right with equivalent pressure settings.
User Weight Limited in 0~250Kg.
(2) MAX Button:
During nursing, it can be difficult to turn a patient and nurse if the
mattress is too soft. This can harden the mattress in the quickest way
for easy nursing. However, after 30 minutes, the unit will forcefully
resume the setting before the button is pressed in order to protect
the patient from the risk of developing pressure ulcers because the
mattress becomes too hard. Press the button when necessary.

12
(3) Audible Mute Button:
The alarm becomes audible when Low Pressure Alarm problem
occurrence. The alarm can be muted with this button when it is
necessary to turn off the function of the alarm sound.
But after 7 minutes the alarm will detect and sound again if still low
pressure.
LED Indicate Area
(1) Low Pressure Alarm Indicate:
When Low Pressure Alarm occurrence, orange indicator is on.
Lights will be on until the issue is solved.
*But if orange LED is on, the Check symbol LED will not light up.
(2) Check Mode Indicate:
Green indicator is blinking it means normal air pumping inside the
mattress.
When check symbol Green indicator is on it means pressure
monitoring and is normal.
*If check LED is on, triangle LED will not light up.
(3) MAX Indicate:
When the green indicator is on, this means that the MAX Button is
activated. Press again and it will cancel. Or after 30 minutes it will
auto cancel and back to the last settings.

13
9. Routine Maintenance and Cleaning
1. Avoid using the unit when the air is poor. Do not smoke especially
to prevent nicotine and greasy tar-like substance from entering the
unit and resulting in the deterioration of internal pipes and the need
for frequent replacement of the air cotton filter.
2. Thoroughly wipe down the dust or smear stuck on the exterior of
the unit with a dry cloth and the 70%-75% ethanol. It is
recommended to clean the pump once a week.. (Caregivers must
wear gloves and masks and protected with disinfection.)
3. An air purifier can also be used to maintain the air quality.
4. Replacement of the air cotton filter: it is recommended to replace
the filter once a month. (Please purchase the filters from the dealer.)
10. Storage
How to store the Air Pump
1. It is necessary to turn off the power switch in side panel , unplug
the power cord.
2. Disconnect the Air Pump and the power cord; disconnect the Air
Pump and the hose at the feet end of the mattress.
3. Put the Air Pump and the power cord in the box and place in a dry
place.
4. When the Air Pump is put away and not in constant use, it is
better to switch it on at regular intervals to lengthen its life.
5. Follow the national requirement to dispose the Air Pump.

14
11. Troubleshooting
Symptom
Inspection Procedure
Possible Solution
1. Air Pump
does not
operate.
1.1) Check if the two
ends of the power
cord are safely
connected to the Air
Pump and the
socket.
1.1) Confirm if the wall
socket has power
supply.
1.2) Check if the power
switch on the side of
the Air Pump is
switched to “ON”.
1.2) If not, switch to “ON”.
1.3) Check if the fuse has
burnt out or not
properly installed.
1.3) Turn off the power
and check the fuse.
2. Air Pump is
working, but
mattress is
not inflating.
2.1) Check if air comes
out of the Air Pump
and if the connector
is properly
connected.
2.1) If the unit operates
normally but no air
comes out, it is
possible that the Air
Pump has something
wrong inside and
needs repair.
2.2) Check if the CPR lid
falls off.
2.2) Repair or replacement
is needed if the lid is
damaged.
2.3) Check if the mattress
connector is bent or
falls off.
2.3) Repair or replacement
is needed if the
connector is deformed
and cannot be
restored or the
material is not in its
normal state.

15
2.4) Check if the air hose
is damaged.
2.4) Repair or replacement
is needed if the air
hose is damaged.
2.5) Check if the air
cotton filter is
heavily soiled and
the air is blocked.
2.5) Replace the filter if it is
heavily soiled.
3. Bottom in
contact with
the overlay
3.1) Check weight
setting.
3.1) Increase weight
setting.
3.2) Check if air leaks
from the mattress.
3.2) Replace the air cells if
damaged.
3.3) Check if the air
cotton filter is
heavily soiled and
the air is blocked.
3.3) Replace the filter if it is
heavily soiled.
4. Others
Problems other than the
above.
Contact the local
distributor for handling.

16
12. Technical Specifications
Air Pump
Power Input : AC220-240V,50/60Hz or AC100-120V,60Hz
Power Consumption: 10W max
Fuse Rating: T1AL/250V
Weight: 1.5Kg (approx.)
Dimension: L26cm*W8cm*H13cm
Air flow rate : 6-8 liter/min (approx.)
Pressure Control Range: 20-50mmHg (+/-5)
Air Mattress
The air pump only use with the air mattress that
manufacturer provided together. If in doubt, please
contact the manufacturer for more information.
4”cells mattress loading weight: 30-120kg
5”cells mattress loading weight: 30-150kg
6”cells mattress loading weight: 30-180kg
8”cells mattress loading weight: 30-200kg / 30-250kg optional
Environment Condition:
Usage
Transport
Storage
Temperature
5 °C ~40 °C
-25°C ~ 70 °C
-25 °C ~70 °C
Humidity
15% to 93%
- 25 °C without relative
humidity control; and + 70 °C at
a relative humidity up to 93 %,
non-condensing
Atmospheric
Pressure
700hPa to
1060hPa
500hPa to
1060hPa
500hPa to
1060hPa
Air Pump Expected Service Life: 5 years.

17
13. EMC table
Guidance and manufacturer’s declaration – electromagnetic
emissions
The model TS-S00 is intended for use in the electromagnetic
environment specified below. The customer or the user of the
model TS-S00 should assure that it is used in such an environment.
Emissions test
Compliance
Electromagnetic environment
– guidance
RF emissions
CISPR 11
The model TS-S00 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
The model TS-S00 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.
Harmonic
emissions
IEC 61000-3-2
Voltage
fluctuations/
flicker emissions
IEC 61000-3-3

18
Recommended separation distances between
portable and mobile RF communications equipment and the model
TS-S00
The model TS-S00 is intended for use in an electromagnetic
environment in which radiated RF disturbances are controlled. The
customer or the user of the model TS-S00 can help prevent
electromagnetic interference by maintaining a minimum distance
between portable and mobile RF communications equipment
(transmitters) and the model TS-S00 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
d = 1,2
80 MHz to
800 MHz
d = 1,2
800 MHz to 2,5 GHz
d = 2,3
0,01
0,12
0,12
0,23
0,1
0,38
0,38
0,73
1
1,2
1,2
2,3
10
3,8
3,8
7,3
100
12
12
23
For transmitters rated at a maximum output power not listed above,
the recommended separation distanced in meters (m) can be
estimated 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 reflection
from structures, objects and people.
P
P
P

19
Guidance and manufacturer’s declaration – electromagnetic
immunity
The model TS-S00 is intended for use in the electromagnetic
environment specified below. The customer or the user of the
model TS-S00 should assure that it is used in such an environment.
Immunity test
IEC 60601
test level
Compliance
level
Electromagnetic
environment –
guidance
Electrostatic
discharge
(ESD)
IEC 61000-4-2
±6 kV
contact
±8 kV air
±6 kV
contact
±8 kV air
Floors should be
wood, concrete or
ceramic tile. If
floors are covered
with synthetic
material, the
relative humidity
should be at least
30 %.
Electrical fast
transient/burst
IEC 61000-4-4
±2 kV for
power
supply lines
±1 kV for
input/output
lines
±2 kV for
power
supply lines
±1 kV for
input/output
lines
Mains power
quality should be
that of a typical
commercial or
hospital
environment.
Surge
IEC 61000-4-5
±1 kV line(s)
to line(s)
±2 kV line(s)
to earth
±1 kV line(s)
to line(s)
±2 kV line(s)
to earth
Mains power
quality should be
that of a typical
commercial or
hospital
environment.
interruptions
and
voltage
variations
<5 % UT
(>95 % dip in
UT)
for 0,5 cycle
<5 % UT
(>95 % dip in
UT)
for 0,5 cycle

20
on power
supply
input lines
IEC
61000-4-11
40 % UT
(60 % dip in
UT)
for 5 cycles
70 % UT
(30 % dip in
UT)
for 25 cycles
<5 % UT
(>95 % dip in
UT)
for 5 sec
40 % UT
(60 % dip in
UT)
for 5 cycles
70 % UT
(30 % dip in
UT)
for 25 cycles
<5 % UT
(>95 % dip in
UT)
for 5 sec
Power
frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
3 A/m
3 A/m
NOTE UT is the a.c. mains voltage prior to application of the test
level.
Guidance and manufacturer’s declaration – electromagnetic
immunity
The model TS-S00 is intended for use in the electromagnetic
environment specified below. The customer or the user of the
model TS-S00 should assure that it is used in such an environment.
Immunity
test
IEC
60601
test
level
Compliance
level
Electromagnetic
environment – guidance
Portable and mobile RF
communications equipment