Pure Global

Refobacin® Bone Cement R - Orthopaedic cement, medicated - ARTG 450208

Access comprehensive regulatory information for Refobacin® Bone Cement R - Orthopaedic cement, medicated in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 450208 and sponsored by Zimmer Biomet Pty Ltd, manufactured by Biomet France in France. The device registration started on May 30, 2024.

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.

Free Database
Powered by Pure Global AI
TGA ARTG Official Data
Class III
ARTG 450208
Class III
Refobacin® Bone Cement R - Orthopaedic cement, medicated
ARTG ID: 450208
Good Name: Zimmer Biomet Pty Ltd - Refobacin® Bone Cement R - Orthopaedic cement, medicated
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Intended Purpose

Refobacin® Bone Cement R is indicated to be used for stable anchoring of suitable joint prostheses to the bone, in hip and knee primary arthroplasty operations, also in case an infection with gentamicin-sensitive strains is a potential risk.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
450208
Start Date
May 30, 2024
Effective Date
May 30, 2024
Manufacturer
Country
France
Address
Plateau de Lautagne, Valence, 26000