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Rotary/reciprocating endodontic file/rasp, single-use

Access comprehensive regulatory information for Rotary/reciprocating endodontic file/rasp, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Henry Schein Halas, manufactured by Micro Mega SA in France. The device registration started on September 23, 2020.

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 IIa
Class IIa
Rotary/reciprocating endodontic file/rasp, single-use
Australia TGA ARTG Registered Device
Good Name: Henry Schein Halas - Rotary/reciprocating endodontic file/rasp, single-use
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Intended Purpose

The medical device Remover is a Nickel-Titanium instrument used for the desobturation/removal during a non-surgical endodontics retreatment in continuous rotation

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
September 23, 2020
Effective Date
September 23, 2020
Manufacturer
Country
France
Address
12 rue du Tunnel, Besancon, France, 25000