Non-sterile scar management dressing, reusable - ARTG 209830
Access comprehensive regulatory information for Non-sterile scar management dressing, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 209830 and sponsored by Total Patient Care Pty Ltd, manufactured by Biodermis in United States of America. The device registration started on May 22, 2013.
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 non-sterile covering made of a silicone-based material (e.g., silicone gel) that is applied directly to the skin for the management of hypertrophic or keloid scars. The device is typically in the form of an elastic sheet that occludes the skin to hydrate and reduce red, dark, or raised scars resulting from surgery, accidents, cuts, burns, or other injuries. The device may be self-adhesive or fixed by tape; it may be washable. This is a reusable device.