Dressing, wound-nonadherent, permeable - ARTG 337132
Access comprehensive regulatory information for Dressing, wound-nonadherent, permeable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 337132 and sponsored by Sentry Medical Pty Ltd, manufactured by Shanghai ISO Medical Products Co Ltd in China. The device registration started on May 27, 2020.
This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.
The dressing is intended for use as a primary contact layer where wound tissue or surrounding skin has been identified as sensitive or fragile. Its silicone coating prevents adherence, thereby reducing potential damage to, or removal of, tissue, and the pain dressing removal may cause. As the pores enable exudate drainage, it can be used on wounds with any level of exudate, including dry or non-exuding wounds. It can be used with other wound care products or medications to manage a variety of wound conditions and types.