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Invacare Softform
Premier Active 2
Active 2 Pump Service Manual
EN
Mattresses
User Manual
DE
Matratzen
Gebrauchsanweisung
FR
Matelas
Manuel dutilisation
ES
Colchones
IT
Materassi
Manuale duso
PT
Colches
Manual de instrues
SV
Madrasser
Bruksanvisning
NO
Madrasser
Brukerveiledning
DA
Madrasser
Brugsanvisning
1|Page
2|Page
CONTENTS PAGE
General
Symbols
Intended Use
Service Life
Guarantee
Standard Invacare Terms
Quality and Flame Retardancy
Product Description
Features
Technical Specifications
10
Tools Required
11
12
13
3|Page
15
16
17
18
20
21
22
23
24
26
27
28
Section 16 Troubleshooting
29
31
4|Page
General
1.1
Symbols
Signal words are used in this manual and apply to hazards or unsafe practices which could result in
personal injury or property damage. See the information below for definitions of the signal words.
Warning indicates a potentially hazardous situation which, if not avoided, could result in death or
serious injury. Caution indicates a potentially hazardous situation which, if not avoided, may result in
property damage or minor injury or both.
Indicates a hazardous situation that could result in damage to property if it is not avoided.
Gives useful tips, recommendations and information for efficient, trouble-free use.
This product complies with Directive 93/42/EEC concerning medical devices. The launch date of this
product is stated in the EC declaration of conformity.
5|Page
1.2
Intended Use
This pressure redistribution mattress and pump is intended to be used in conjunction with an appropriately
sized bed frame, as part of an overall pressure ulcer prevention program of care. It can be used safely in
static mode (deflated) for static pressure redistribution, or in dynamic mode (inflated) should an
alternating pressure support surface be required. This product has been designed to deliver effective
pressure reduction to users, when the product is in normal use which is defined by Invacare Ltd as when
the support surface is covered with a cotton, cotton combination or linen bed sheet, and any one of these
would be the only item deployed between the support surface and the user.
1.3
Service Life
We estimate a life expectancy of five years for these products, provided they are used in strict
accordance with the intended use as set out in this document and all maintenance and service requirements
are met.
The estimated life expectancy can be exceeded if the product is carefully used and properly maintained,
and provided technical and scientific advances do not result in technical limitations. The life expectancy
can also be considerably reduced by extreme or incorrect usage. The fact that we estimate a life
expectancy for these products does not constitute an additional warranty.
1.4
Guarantee
We provide a manufacturers warranty for the product in accordance with our General Terms and
Conditions of Business. Guarantee claims can only be made through the relevant specialist dealer.
1.5
This is to certify that your Softform Premier Active 2 Mattress is warranted by Invacare Ltd for a
period stated in the Table Technical Data of this user guide. The Warranty of your Invacare
Softform product is valid from time of shipping. If a defect or fault is discovered the Invacare dealer
or Local Business
Development Manager from whom the appliance was obtained must be notified immediately. The
manufacturer will not accept responsibility for damage caused by misuse or non-observance of the
instructions set out in this user guide. During the period of the warranty any products that have become
defective due to faulty workmanship or materials will be renewed without charge. The warranty will be
forfeited should any unauthorized alteration be made to the equipment. Both warranty and fire retardancy
Certification will become null and void if non-Invacare spares are used on any Invacare Softform
Mattress products.
The purchasers statutory rights under the Consumer Protection Act are not affected.
1.6
1.7
Product Description
7|Page
The Softform Premier Active 2 mattress system acts as a static pressure reducing support/mattress
for patients at high risk that can, by facilitating the air pump, introduce effective alternating pressure if
the patients condition requires alternating pressure therapy. The water-resistant cover provides a
vapour-permeable, multi stretch surface, to promote patient comfort and to maximise the effectiveness
of the foam core. The complete system comprises of:
A mattress insert comprised of alternate air cells that connect to a twin air connector hose.
A Micro-processor controlled air pump unit.
A 5 metre power lead.
8|Page
Features
Main Enclosure
Technical Specifications
Main Supply
220/240V AC, 50 Hz
1 Amp
Supply Fuse
1 Amp
Noise Level
< 32 db
Classification
Class 2 Type BF
Cycle Time
10 Min
Size
Weight
1.75kg
Air Flow
4 l/min
Operating Pressure
60mmHg +- 10%
Power
10W
Warranty on pump
24 Months
24 Months
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Tools Required:
1 x ESD mat and strap (Recommendation RS components 681-1235)
1 x Phillips screwdriver
1 x Flat head screwdriver
1 x 4BA Open end spanner
1 x Bloc Lube Red (RS components 196-5245)
1 x Snips
2 x Sphygmomanometers (Pressure test kit)
1 x Active2 Air insert
1 x Star lock Applicator
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unit.
Figure 2.1
the
Figure 2.2
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Yes
Not working
Fixed
working
Faulty micro
power PCB
Not
OK
Replacement of
Yes
switch. Replace
Rotor PCB
Return to
Not working
manufacturer/
Supplier
Fixed
OK
Systems ok
(10mins)
OK
Pump is ok for
use.
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Fixed
Pump alarms
with Rotor
Failure on the
Replace Rotor
Return to
PCB
manufacturer/
Supplier
Display Screen
No
Pump is alarming
with Low
Pressure on the
display screen
Yes
mattress CPR
Pressure test
connector is
securely attached
Fixed
Rotor PCB
No
pressure
Faulty
No
Fixed
Transducer.
Check/replace
Replace Display
compressor
Replace Display
PCB
Fixed
PCB
Fixed
Display screen
Ok
to the unit.
Fixed
Fixed
No display txt on
No pressure
Not Working
Return to
manufacturer/
Supplier
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Securing screws
Phillips screwdriver
2-
3.
Figure4.1. Remove
Rear lid
Securing screws
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Figure 5.1
the
and
the
Spare
Fuse
Figure 5.2
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Figure 6.2
Figure 6.3
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Figure 7.1
Figure 7.2
Figure 7.3
Figure 7.5
Figure 7.6
Figure 7.7
Figure 7.4
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cap.
Black plastic
cap
1.
2.
3.
4.
5. Remove the 2 screws that secure the power PCB board to the case enclosure.
Figure 8.2
6. Gently pull the power PCB board towards the back of the case ensuring you do
not damage 5 pin female connections that connects to the Rotor PCB 5 pin
male. Figure 8.3
7. To re-install power PCB board and plastic cap, reverse steps 2-6.
8. Run the pump to ensure it works.
Figure 8.3
20 | P a g e
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transducer
tube
Figure 9.1
Finger brackets
and
Figure 9.2
Top
Middle
Bottom
Figure 9.3
Figure 9.4
NOTE: For this procedure, refer to figures 10.1 to 10.4, and 8.1 Page 21.
DANGER
To prevent electrical shock, ALWAYS disconnect from the power supply before removing the rear lid.
Tools required 1 x Phillips screwdriver.
1 x Snips.
Cable
Cable tie x1
tie x2
Figure 10.1
Figure 10.2
23 | P a g e
Figure 11.1
Unplug from the power supply.
Remove the rear lid. Refer to Case enclosure and rear lid on page 15.
Cut the cable tie shown on figure 11.1
Carefully pull the air tube away ensuring you do not snap the plastic rivets.
Remove the yellow capillary tube from the transducer on the Display PCB.
Figure 11.2
Remove the compressor power supply. Figure 11.3
Remove the compressor.
Compressor power supply
To re-install reverse steps 2-10.
Figure 11.3
Run the pump to ensure it works.
Figure 11.2
24 | P a g e
Figure 12.1
1. Connect the pump Male CPR connector to the female cross connector.
2. Connect the Active2 Air insert female connector to the male cross connector.
3. Connect the Sphygmomanometers to the 2 pipes (one each side) Figure 12.2,
Please ensure an air tight fit.
4. Ensure that the Sphygmomanometers are turned on.
5. Connect the Active2 Pump to the mains and switch on. Please allow 10minutes
for the system to setup.
Figure 12.2
6. When the pump has settled and displaying System OK on the display screen, Inspect the air pressures
on the sphygmomanometer over a short period to ensure the pump is hitting the correct pressures and
25 | P a g e
alternating.
7. The air pressure should be at 60mmHg =/- 10%. The 10minute cycle is broken down to a 5min/5min section
which makes up the 10min cycle.
8. The air pressure on the sphygmomanometers should also mirror what pressures have been selected on the
display screen. Figures 12.3 and 12.4
Figure 12.3
Figure 12.4
9. Monitor the pressures for at least one full cycle (10 minutes)
10. Finish testing by switching the pump off and disconnecting the test equipment.
11. If the air pressures fail to meet the specified requirements during the stage of pressure testing, firstly
check for any leaks on the test equipment (connections/air cells). If your checks pass without any leaks
detected please proceed to the Page 14 Service Procedure Flowchart (Pump is alarming with Low
Pressure on the display screen) for further indication.
Please note that the Air pressure is defaulted at 60mmHg if the pump is turned off and switched back on.
26 | P a g e
Figure 13.1
Figure 13.2
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Figure 14.1
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Figure 15.1
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Section 16 Troubleshooting
Fault
Cause
Initial Checks
No Power (Continuous
alarm)
Power cord
disconnected
Replace fuse
Check compressor
Rotor Failure
(Buzzer is beeping)
Micro switch
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Section 16
User manual Pump Menu Display
Task
1. Power up.
Action
Switch pump on.
Display
3 Audible beeps and LCD illuminates and
green light illuminates.
System set up displayed.
After 5 to 10 minutes System OK
displayed.
2.Menu option
3. Disconnection of CPR or
hose in mattress
disconnected.
32 | P a g e
Pressure displayed.
Press OK.
33 | P a g e
Invacare UK Ltd.
Pencoed Technology Park, Pencoed, Bridgend, CF35 5AQ,
UK_Tel: +44 1656 776200 Fax: +44 1656 776201
Technical Services Tel: +44 1656 776333 Fax: +44 1656 776330
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