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Wound retractor, intermediate/deep

Access comprehensive regulatory information for Wound retractor, intermediate/deep in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Zimmer Biomet Pty Ltd, manufactured by Biomet UK Ltd in United Kingdom. The device registration started on May 04, 2018.

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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Class I
Class I
Wound retractor, intermediate/deep
Australia TGA ARTG Registered Device
Good Name: Zimmer Biomet Pty Ltd - Wound retractor, intermediate/deep
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Intended Purpose

A hand-held, non-self-retaining surgical instrument intended to be used to separate/draw aside the margins of a wound/incision to allow access to tissues/organs during open surgery; It includes a shaped/hooked blade with a handle/holding portion and is available in a wide variety of designs, such as a double- or single-ended blade that may be fenestrated (pronged); deep wound retractors are typically designed with a long, curved blade that may also be intended to retract organs; it may include a light. This is a reusable device.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
May 04, 2018
Effective Date
May 04, 2018
Manufacturer
Country
United Kingdom
Address
Waterton Industrial Estate, Bridgend, South Glamorgan, CF31 3XA