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Tourniquet cuff bandage, non-latex - ARTG 481611

Access comprehensive regulatory information for Tourniquet cuff bandage, non-latex in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class Is is registered under ARTG number 481611 and sponsored by Zimmer Biomet Pty Ltd, manufactured by Zimmer Surgical Inc in United States of America. The device registration started on March 04, 2025.

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 Is
ARTG 481611
Class Is
Tourniquet cuff bandage, non-latex
ARTG ID: 481611
Good Name: Zimmer Biomet Pty Ltd - Tourniquet cuff bandage, non-latex
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Intended Purpose

A sterile single use device intended to help protect a patientโ€™s limb during tourniquet cuff use from possible wrinkling, pinching and shearing of skin and soft tissues.

Device Classification
Risk Class
Class Is
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
481611
Start Date
March 04, 2025
Effective Date
March 04, 2025
Manufacturer
Country
United States of America
Address
200 W Ohio Avenue, Dover, OH, 44622