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Reamer, orthopaedic

Access comprehensive regulatory information for Reamer, orthopaedic in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by OrthoCentric Pty Ltd, manufactured by OrthoCentric Pty Ltd in Australia. The device registration started on February 16, 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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Class I
Class I
Reamer, orthopaedic
Australia TGA ARTG Registered Device
Good Name: OrthoCentric Pty Ltd - Reamer, orthopaedic
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Intended Purpose

A manual orthopaedic surgical instrument used to open and enlarge the medullary canal for the insertion of various devices during prosthesis implantation or fracture fixation procedures.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
February 16, 2023
Effective Date
February 16, 2023
Manufacturer
Country
Australia
Address
21/76 Reserve Road, ARTARMON, NSW, 2064