End Of Life Disposal - arjo Flowtron Instrucciones De Uso

Indications
•
• Enhancement of venous & arterial
circulation.
•
• Assistance in the healing of cutaneous
ulcers, including venous ulcers.
• Reduction of acute & chronic edema.
• Reduction of lower limb pain due to trauma
or surgery.
• Reduction of compartment pressures.
Contraindications
IPC should not be used in the following
conditions
•
vascular diseases.
•
•
heart may be detrimental.
•
• Any local condition in which the garments
would interfere, including gangrene, recent
skin graft, dermatitis or untreated, infected
leg wounds.
• If you are unsure of any contraindications
refer to the patient's physician before using
the device.
Serious Incident
If a serious incident occurs in relation to this
then the user or patient should report the serious
incident to the medcial device manufacturer or
the distributor.
report the serious incident to the Competent
Authority in the member state where they are
located.
Recommendations
• Continuous intermittent pneumatic compres-
sion is recommended until the patient is fully
is recommended.
• In the non-surgical patient, the system
should be initiated immediately once the risk
• Garments should be removed regularly
to inspect the skin for signs of redness or
pressure points.
Cautions
• Garments should be removed immediately
if patient experiences tingling, numbness or
pain.
•
use is recommended and any interruption
of therapy for a substantial length of time
should be at the discretion of physician.
•
walk with the foot garments on.
• This product cannot be adequately cleaned
and / or sterilized by the user in order
to facilitate safe reuse and is therefore
intended for single patient use. Attempts to
clean or sterilize these devices may result in
a biocompatibility, infection or product failure
risk to the patient.

End of Life Disposal

Garment material or any other textiles, polymers
or plastic materials etc. should be sorted as
combustible waste.
CE marking indicating conformity with
European Community harmonised
legislation
Indicates the product is a Medical
EN
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