Use Instructions

Instructions for Use | Anti-Decubitus Air Alternating Pressure Mattress Replacement System
AVA Activity Analytics
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1.4 Purpose of the Device
To ensure the security of patients and users, the device may only be
used for its intended use.
1.4.1 Intended Use
The therapeutic air alternating mattress / cushion system is designed
for patients who endure pressure ulcer and potential patients who wish
to reduce the likelihood of pressure ulcer. The device is intended to
treat and prevent pressure ulcers by facilitating blood circulation and
decreasing pressure of each tissue's contact area.
Contraindications:
Certain patient conditions are not suitable for using this type of
device such as fracture of instable vertebrae and illness of instable
vertebrae. Always consult a physician or health professional before
using this device. The use of this system does not replace the regular
repositioning, monitoring, and nursing of the patient.
1.4.2 Attention
Always consult a physician or health professional before using the
AVA Activity Analytics System. Any and all applications outside of the
conditions specified above are regarded as unapproved. The user
and the operator respectively are exclusively liable for any damage
resulting from the unapproved use.
Additional safety points to be aware of:
Strangulation by extra-long cables and hoses. To avoid
entanglement, keep children clear of hoses.
A Warning indicating that replacement by inadequately trained
personnel could result in hazard.
Do not expose the Home Healthcare System to the sunlight or the
dusty environment.
Keep the Home Healthcare System out of reach of children.
Choking caused by small parts being inhaled or swallowed Identify
any loose or detached small parts that may be an issue.
Potential allergic reactions to materials used in the equipment
Identify any rubber or latex that could be an issue.
Contact Injuries
Check for any skin irritation due to prolonged contact with the
equipment.
Expected service life of this medical air pump is 2 years.
Protection against strangulation or asphyxiation
Means shall be provided to control the risk of strangulation and
asphyxiation of the patient and other to an acceptable level by
routing wires or tubings, and using retention devices.
No modication of this system is allowed.
Intended use
Attention
Important Notes for Safe Use
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