Australia TGA ARTG record

Synthetic polymer semi-permeable film dressing, wound-nonadherent

Australia TGA ARTG Registered Device · Device Services Australia Pty Ltd · Reskin Medical nv · Class I · Started March 24, 2020

Good Name: Device Services Australia Pty Ltd - Synthetic polymer semi-permeable film dressing, wound-nonadherent

Device classification

Risk Class: Class I
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: March 24, 2020
Effective Date: March 24, 2020

Sponsor

Name: Device Services Australia Pty Ltd

Manufacturer

Name: Reskin Medical nv
Country: Belgium
Address: Poort West-Limburg 1399 Industrieweg 114, Tessenderlo, 3980

Intended purpose

A non-sterile, single-use, transparent, semi-permeable covering applied to wounded or diseased tissue intended to provide protection and/or promote healing. It may be applied directly to tissue or used in combination with other dressings to protect skin or wounds from microbial or other contamination and from fluid strikethrough.

About this record

Access comprehensive regulatory information for Synthetic polymer semi-permeable film dressing, wound-nonadherent in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Device Services Australia Pty Ltd, manufactured by Reskin Medical nv in Belgium. The device registration started on March 24, 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.