ANTI-DECUBITUS AIR ALTERNATING PRESSURE CUSHION REPLACEMENT SYSTEM
3
English
1.0 Indications
Attention! Please read enclosed
document thoroughly
Authorized Representative
Declaration of Conformity to
Medical Device Directive
Type BF Equipment
Double insulated (Class II)
Dissposal of Electrical &
Electrical Equipment (WEEE)
Manufacturer
Date of manufacture
Catalog number
Protected against solid foreign
objects up to 12.5mm diameter
(finger) and protected against
vertically dripping water.
Machine Wash Warm (Max. 71°C)
Tumble Dry Medium-Gentle
Cycle
DO NOT Iron
DO NOT Dry Clean
DO NOT Bleach
SGS Q certification mark
Indications
This anti-decubitus air alternating
pressure cushion replacement system
is designed for patients who are at high
risk for pressure ulcer to be placed in a
variety of mobile devices and potential
patients who wish to reduce the likelihood
of pressure ulcer. This device is intended
to prevent pressure ulcers by facilitating
blood circulation and decreasing pressure
of each tissue’s contact area. If there’s
any question, please always consult a
physician or health professional before
using this device.
Contraindications
Certain patient conditions (e.g. unstable
cervical fracture, fracture of unstable
vertebrae and illness of unstable
vertebrae) are contraindicated for use with
this device. If there’s any question, please
always consult a physician or health
professional before using this device.
Users
The device should only be used by people
who have been trained in operation and
intended use of the device.
The trained users on the operation and
the dedicated use of the device must
be carried out by the qualified operator
before using the device.
Users are fully responsible for the safe
and correct use of the device. A review of
the functions should be carried out and the
proper conditions of the device should be
checked and confirmed by the user before
each use or transfer for use.
IP22
710262