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Bone graft funnel - ARTG 474469

Access comprehensive regulatory information for Bone graft funnel in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 474469 and sponsored by Medtronic Australasia Pty Ltd, manufactured by Medtronic Sofamor Danek USA Inc in United States of America. The device registration started on December 23, 2024.

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 474469
Class I
Bone graft funnel
ARTG ID: 474469
Good Name: Medtronic Australasia Pty Ltd - Bone graft funnel
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Intended Purpose

An orthopedic manual surgical instrument intended for use in surgical procedures to deliver bone graft filling material.

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
474469
Start Date
December 23, 2024
Effective Date
December 23, 2024
Manufacturer
Country
United States of America
Address
1800 Pyramid Place, Memphis, Tennessee, 38132