Technical Data - Stryker CF302 Sof-Care Notice D'utilisation

English
CF302 Series Inflation Unit
Instructions for Use
Figure 1
Figure 2
CONTRAINDICATIONS
Air support therapy is not recommended when spinal stability is a concern.
INDICATIONS
The Sof·Care ® Care·Free ® Companion Pump (CF302) Series is for use with
®
only Gaymar Sof·Care and duo·gard
designed to assist in the prevention and treatment of pressure ulcers.
The Sof·Care ® Care·Free ® Companion Pump (CF302) unit will inflate and
maintain Sof·Care ® overlays at therapeutic pressure levels, even when minor
punctures occur. The Sof·Care ® overlay redistributes the patient's weight
over the surface and effectively reduces tissue interface pressure.
SAFETY PRECAUTIONS
DANGER
If a bulge in the top surface of the overlay is noticed, discontinue use and
call your dealer.
A bulge may cause the patient to roll over when not desired, potentially
resulting in serious injury or death.
CAUTION
• Check patient's skin regularly. Consult physician if any redness or skin
break occurs. Serious injury could result if the patient's skin condition
is left untreated.
• Do not place the pump in the patient's bed, in contact with the patient,
or under sheets or other coverings. This could cause serious injury or
could affect pump performance.
INSTRUCTIONS
1. Set up overlay and pump as shown in Figure 1. Place corner straps
around bed mattress.
2. Place the pump near the bed. If placing it on footboard, place the unit
on the outside (not the patient side), with the rubber feet against the
footboard as shown in Figure 2.
3. Turn unit on using illuminated on/off switch. Unit will take
approximately 40 minutes to inflate the overlay.
4. Place the patient on the overlay and set the comfort control knob to the
appropriate setting based on patient comfort.
5. Perform Hand Check.
A Hand Check must be performed every 8 hours to verify proper
operation.
To perform the Hand Check:
With the patient on his or her back, slide hand, flat and palm up,
between the overlay and the mattress. Hand should be directly under
the air cell that is under the patient's buttocks (or other bony area).
2012/09
®
overlays. These products are
101099 Rev D.0
HAND CHECK
Properly inflated
If the patient's body is not in direct contact with hand, the system is
operating correctly. The patient's body is in direct contact with flat hand, the
system is not operating properly. Adjust the pressure control to a higher
setting. Wait 10 minutes and repeat the Hand Check. If the Hand Check fails,
check that the hoses are not kinked or pinched. If repeated Hand Check fails
and hoses are not kinked, contact Dealer or Gaymar for further instruction.
CPR DEFLATE.
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WARNING
Deflate before CPR or CPR will be ineffective.
CLEANING
The pump housing should be cleaned between patients.
Before cleaning, unplug the pump. Clean housing with a mild detergent and
damp cloth. Wipe pump dry with a clean cloth before operating. Do not
submerge. Do not autoclave.

TECHNICAL DATA

Voltage: 230 VAC
Current: 0.05A
Wattage: 10 Watts
Overcurrent Protection: Fused, Rated 1A 250 VAC
Frequency: 50 Hz
Operating Temperature: 15°C to 32°C, (60°F to 90°F)
Classification:
• EN 60601-1, EN 60601-1-2
• IPXO, enclosed equipment without protection against ingress of water
• Not suitable for use in the presence of a flammable anaesthetic mixture
with air or with oxygen (O2) or nitrous oxide (N2O).
• Continuous operation
The control unit is warranted for one (1) year.
SYMBOLS
Caution, consult
accompanying
documents
Dangerous voltage
Type BF equipment
CUSTOMER SERVICE
If you have purchased this pump through a local dealer and are experiencing
problems, please contact that local dealer for assistance. For additional
assistance, contact our Customer Service Department at:
Stryker Medical, 3800 East Centre Avenue, Portage, Michigan 49002 USA
Telephone: 1-800-327-0770
Under-inflated
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Double Insulation
Consult Operating Instructions
Disposal: Contact local
distributor who will take the
necessary steps according to
your national market.
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