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Skin semi-occlusive dressing, non-sterile, antimicrobial

Access comprehensive regulatory information for Skin semi-occlusive dressing, non-sterile, antimicrobial in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Ausmed Supplies Pty Ltd, manufactured by Kerecis AG in Switzerland. The device registration started on April 20, 2022.

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 IIb
Class IIb
Skin semi-occlusive dressing, non-sterile, antimicrobial
Australia TGA ARTG Registered Device
Good Name: Ausmed Supplies Pty Ltd - Skin semi-occlusive dressing, non-sterile, antimicrobial
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Intended Purpose

A non-sterile substance intended to be topically applied to injured skin, where the dermis is breached to expedite skin healing and re-epithelialization primarily through semi-occlusive properties which reduce moisture transmission from the wound to the environment by means of a physical barrier; it also includes an antimicrobial agent(s). For home/healthcare facility use to treat open skin wounds (e.g., abrasions, lacerations, burns, surgical wounds, ulcers) and/or conditions (e.g., eczema, psoriasis, scars.

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
April 20, 2022
Effective Date
April 20, 2022
Manufacturer
Country
Switzerland
Address
Webereistrasse 61, Adliswil, 8134