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Periotome, reusable - ARTG 162182

Access comprehensive regulatory information for Periotome, reusable in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 162182 and sponsored by Medi-Dent Pty Ltd, manufactured by PDT Inc in United States of America. The device registration started on June 03, 2009.

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 162182
Class I
Periotome, reusable
ARTG ID: 162182
Good Name: Medi-Dent Pty Ltd - Periotome, reusable
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Intended Purpose

For use in dentistry during tooth extraction to cut the periodontal ligament that binds the tooth to the surrounding marginal and alveolar bone to reduce trauma to the surrounding tissue.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
162182
Start Date
June 03, 2009
Effective Date
June 03, 2009
Manufacturer
Country
United States of America
Address
8275 Highway 10 West, Missoula, MT, 59808