More Details

Materials
* Foam base
* Gel cube pad overlay

Cover
* Removable washable stretch

Application
* The supplier states that the cushion is suitable for users requiring mild to moderate postural pelvic support.

Considerations

* All cushions must be monitored to prevent 'bottoming out'. This occurs when the user's weight bears down so hard on the product material that it is flattened and the bony parts are pressed against the surface below the cushion. Where bottoming out occurs even with correct use (eg correct choice and depth of foam, correct inflation level) , a different product may need to be considered.
* The gel cells or fluid on the top layer of the cushion can be punctured
* Ensure that the item is not accidentally placed upside down or back to front.
* It is advisable that a health professional be consulted when considering a suitable pressure care product.

Place Of Manufacture

Novis Healthcare brand from various sites but mostly Asia or Europe

Price Guide

Price is from Novis Healthcare

Models

Only one model available - Gel Seat Pad Code WSGS9641

Standards

Standards
Some assistive technology needs to meet Australian or other standards. Standards may relate to materials, manufacturing and installation. Products that meet Australian or international standards will have written certification. To find out if a product meets Australian Standards ask the supplier to show you the certificate. For more information about standards also see
http://at-aust.org/home/assistive_technology/standards.html

TGA
Many of the items on the Assistive Technology Australia website are categorised as a Medical Device. Medical devices that are approved for use in Australia have been entered into a national database called the Australian Register of Therapeutic Goods (ARTG), which is maintained by the Therapeutic Goods Administration (TGA). You can ask the supplier for the ARTG number for the device you wish to purchase and search the ARTG for the entry. To access information on the ARTG visit www.tga.gov.au

When buying a medical device it is advisable to only choose a medical device that is recommended by a healthcare professional and has been included on the ARTG.

Please note that custom made devices are not required to undergo pre-market assessment by the TGA or to be included on the ARTG before supply. Custom made medical devices do not include medical devices that have been adapted or modified to accommodate an individual patient.