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Retractor, <specify> - ARTG 395996

Access comprehensive regulatory information for Retractor, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 395996 and sponsored by Hallmark Surgical Ltd, manufactured by Dorr Kampen bv in Netherlands. The device registration started on September 15, 2022.

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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Class I
ARTG 395996
Class I
Retractor, <specify>
ARTG ID: 395996
Good Name: Hallmark Surgical Ltd - Retractor, <specify>
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Intended Purpose

Silicone Hand Immobiliser Retractor, as an alternative to the traditional Lead Hand. This device has a lead core but is encapsulated with surgical grade silicone to provide complete protection form any exposure to Lead.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
395996
Start Date
September 15, 2022
Effective Date
September 15, 2022
Manufacturer
Country
Netherlands
Address
Haatlanderdijk 25, Kampen, AN, 8263