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Synthetic polymer semi-permeable film dressing, wound-nonadherent

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.

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TGA ARTG Official Data
Class I
Class I
Synthetic polymer semi-permeable film dressing, wound-nonadherent
Australia TGA ARTG Registered Device
Good Name: Device Services Australia Pty Ltd - Synthetic polymer semi-permeable film dressing, wound-nonadherent
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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.

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
Manufacturer
Country
Belgium
Address
Poort West-Limburg 1399 Industrieweg 114, Tessenderlo, 3980