Australia TGA ARTG record

Dressing, wound-nonadherent, permeable

Australia TGA ARTG Registered Device · Sentry Medical Pty Ltd · Shanghai ISO Medical Products Co Ltd · Class IIb · Started May 27, 2020

Good Name: Sentry Medical Pty Ltd - Dressing, wound-nonadherent, permeable

Device classification

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

Registration information

Start Date: May 27, 2020
Effective Date: May 27, 2020

Sponsor

Name: Sentry Medical Pty Ltd

Manufacturer

Name: Shanghai ISO Medical Products Co Ltd
Country: China
Address: 999 Liuchen Road Pudong New Area, Shanghai

Intended purpose

The dressing is intended for use as a primary contact layer where wound tissue or surrounding skin has been identified as sensitive or fragile. Its silicone coating prevents adherence, thereby reducing potential damage to, or removal of, tissue, and the pain dressing removal may cause. As the pores enable exudate drainage, it can be used on wounds with any level of exudate, including dry or non-exuding wounds. It can be used with other wound care products or medications to manage a variety of wound conditions and types.

About this record

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 Sentry Medical Pty Ltd, manufactured by Shanghai ISO Medical Products Co Ltd in China. The device registration started on May 27, 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.