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Polymer orthopaedic cement restrictor, non-absorbable, sterile - ARTG 430770

Access comprehensive regulatory information for Polymer orthopaedic cement restrictor, non-absorbable, sterile in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 430770 and sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by Depuy International in United Kingdom. The device registration started on December 13, 2023.

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 IIb
ARTG 430770
Class IIb
Polymer orthopaedic cement restrictor, non-absorbable, sterile
ARTG ID: 430770
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Polymer orthopaedic cement restrictor, non-absorbable, sterile
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Intended Purpose

To be inserted into the medullary canal of a bone during orthopaedic surgery to prevent cement progression.

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
430770
Start Date
December 13, 2023
Effective Date
December 13, 2023
Manufacturer
Country
United Kingdom
Address
St Anthony's Road, LEEDS, WEST YORKSHIRE, LS118DT