ARTG 302638Wound retractor, intermediate/deep
ARTG ID: 302638 · Zimmer Biomet Pty Ltd · Biomet UK Ltd · Class I · Started May 04, 2018
Good Name: Zimmer Biomet Pty Ltd - Wound retractor, intermediate/deep
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 302638
- Start Date
- May 04, 2018
- Effective Date
- May 04, 2018
- Name
- Biomet UK Ltd
- Country
- United Kingdom
- Address
- Waterton Industrial Estate, Bridgend, South Glamorgan, CF31 3XA
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.
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 registered under ARTG number 302638 and 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.