This manual should be used for initial set up of the system and for reference purposes.

1.1 GENERAL INFORMATION

The system is a true low-air-loss mattress system suitable for prevention and treatment of Pressure Ulcers up through Stage IV.

The system has been tested and successfully approved with the following standards:

EN 60601-1

EN 60601-1-2

EN 55011 Class B

IEC61000-3-2

IEC 61000-3-3

FOR US AND CANADA ONLY

Medical Equipment-Air Blower

E228589with respect to electrical shock, fire and 53DGmechanical hazards only in accordance with

UL60601-1 AND CAN/CSA C22.2 NO.601.1

Le produit à ététesté avec des équipementsmédicauxetrespecte les normes UL 60601-1 & CAN/CSA C22.2 No.601.1. prévenant les choc électrique, le feu et les risques de blessures physiques.

1.2 INTENDED USE

This product is intended to help treat and reduce the incidence of pressure ulcers from Stage I – Stage IV, while optimizing patient comfort. It is appropriate for use in home care, long term care and acute care settings.

NOTE:Equipment not suitable for use in the presence of a flammable anesthetic mixture with air or with oxygen or nitrous oxide.

NOTE:L’équipement ne peutêtreutilisés’il y a risque de mélange d’un anesthésique inflammable avec l’airoul’oxygèneouoxydenitreux.

3

11

7.3 AIR FILTER REPLACEMENT

1. Replace the air filter locatedat the bottom of blower.

2.The filter is reusable and can be washed gentlywith a mild detergent and water. Dry the filter before use.

3. Check and replace air filterregularly if environment is dirty.

7.4RECHARGEABLE BATTERY

1.To check if the rechargeable battery has been drained out, unplug the power cord andsee if the Power Failure indicator will light up along with buzzer last for a few minutes.

2.If the Power Failure Alarm is unable to work or the battery might need to be replaced(approximate life expectancy 6 months),user can contact your dealer or notify the

technician for replacement.

8. TROUBLESHOOTING

Problem

 

Solution

Power is not ON

 

Check if the plug is connected to mains.

 

Check if there is any blown fuse.

 

 

 

 

 

 

 

Check if the Quick Connector is rotated to the Lock/on position.

Alarm is on

 

Check if the power is suddenly shut down.

 

Check if the connection between air tube connector to blower unit is

(Audible & visual)

 

 

tightly secured.

 

 

 

 

Check if all tubing connections along mattress are secured.

 

 

 

 

 

Pressure setting might be inadequate for thepatient, adjust comfort

Patient is bottoming out

 

range 1 to 2 levels higherand wait for a few minutes for best

 

 

comfort.

 

 

 

 

 

Check if the fowler boost adaptor is connected and secured to the

Automatic fowler boost is

 

blower unit.

not functioning

 

Check if the fowler boost sensor pad tightly snapped to the

 

 

designated location inside the bottom of the mattress foam pocket.

 

 

 

If the above information does not solve your problems, please contact your local agent directly.They might require a technician totake care the problem.

2. PRODUCT DESCRIPTION

Page 4
Image 4
Drive Medical Design 14000 instruction manual Troubleshooting, Product Description