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Bone nail guidewire, single-use

Access comprehensive regulatory information for Bone nail guidewire, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by ConMed Linvatec Australia Pty Ltd, manufactured by ConMed Corporation in United States of America. The device registration started on February 01, 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 IIa
Class IIa
Bone nail guidewire, single-use
Australia TGA ARTG Registered Device
Good Name: ConMed Linvatec Australia Pty Ltd - Bone nail guidewire, single-use
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Intended Purpose

A sterile, single-use, long, thin, metal rod designed to be drilled into bone to create a channel and act as a guide for the implantation of a fracture fixation device such as a nail.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
February 01, 2023
Effective Date
February 01, 2023
Manufacturer
Country
United States of America
Address
525 French Road Utica, New York, 13502-5994