Dressing, wound-nonadherent, permeable
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 sponsored by Device Services Australia Pty Ltd, manufactured by Reskin Medical nv in Belgium. The device registration started on June 15, 2019.
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.
A silicon based sterile wound dressing intended to prevent adherence to the wound bed, thereby decreasing the potential for trauma to the wound and surrounding skin and causing pain upon removal. This is a single-use device.