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Surgical procedure kit, orthopaedic, reusable - ARTG 425931

Access comprehensive regulatory information for Surgical procedure kit, orthopaedic, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 425931 and sponsored by Endocare ANZ Pty Ltd, manufactured by Jiangsu Bonss Medical Technology Co Ltd in China. The device registration started on October 18, 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 I
ARTG 425931
Class I
Surgical procedure kit, orthopaedic, reusable
ARTG ID: 425931
Good Name: Endocare ANZ Pty Ltd - Surgical procedure kit, orthopaedic, reusable
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Intended Purpose

Reusable Surgical Instrument kit used during orthopedic (spinal) surgery

Device Classification
Risk Class
Class I
Product Type
Procedure Pack
ARTG Category
General
Registration Information
ARTG ID
425931
Start Date
October 18, 2023
Effective Date
October 18, 2023
Manufacturer
Country
China
Address
Building #7 No 898 China Medical City Avenue Hailing District, Taizhou City, Jiangsu, 225316