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Connect the pump to the mains power supply using the supplied cable.
Set the 

Run/Standby

 switch (on the side of the pump) to the Run ( 

|

 ) position.

The 

Run/Standby

 indicator is illuminated when the pump is running.

In the event of mains failure, the 

Power Fail

 alarm indicator will start flashing and an audible alarm will sound. 

The pitch of the alarm will increase in time. If the power supply is returned the audible alarm will stop, but the 

alarm light will remain illuminated until the system is reset using the 

Run/Standby

 switch.

The 

Low Pressure 

indicator will flash whenever the pump detects low pressure in the cushion. An audible 

alarm will sound. The pitch of the alarm will increase at 60 second intervals. 
The indicator will extinguish once normal pressure is reached. Check the tubeset is connected properly.

Comfort Control  - 

The seat cushion cell pressure can be manually adjusted for patient comfort using the 

Pressure Control.

Note:

 An internal battery will power an audible and visual alarm if the power supply is interrupted prior to 

switching off. For example, if the mains lead is removed before switching to Standby mode.
The pump alarm can be reset by switching the pump to Standby and back to Run again using the 

Run/

Standby

 switch on the side panel.

This Quick Reference Guide has been produced to assist Healthcare Professionals and other users with only the functional 

aspects of the system. This guide does not replace the general safety warnings, cautions and recommendations provided in 

the product 

Instructions for Use

, part number 500935EN.  

Refer to the product 

Instructions for Use

 before using this product.

Caution

:  Active therapy (alternating) cushions may be unsuitable for patients with poor sitting posture or pelvic deformity; 

advice from a seating specialist should be sought.

Contraindication

: Do not use the system for patients with unstable spinal fractures.

Caution

:  If patients have other unstable fractures, or conditions which may be complicated by a soft or moving surface, 

advice should be sought from an appropriate clinician before use.

Indications:

• 

The Aura cushion is designed for patients weighing up to 120 kg (264 lb).

• 

The Aura systems are indicated for the prevention and/or management of all categories

1

 of pressure ulcer, when 

combined with an individualised, comprehensive pressure ulcer protocol.

1. NPUAP/EPUAP International Pressure Ulcer Guideline, 2014.

Aura

500937EN_03 · 05/2019

QUICK REFERENCE GUIDE

Aura

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