Australia flagARTG 481887

Elevator, orthopaedic, periosteal

ARTG ID: 481887 · Device Technologies Australia Pty Ltd · Scanlan International · Class I · Started March 06, 2025

Good Name: Device Technologies Australia Pty Ltd - Elevator, orthopaedic, periosteal

Device classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration information
ARTG ID
481887
Start Date
March 06, 2025
Effective Date
March 06, 2025
Sponsor
Manufacturer
Country
United States of America
Address
One Scanlan Plaza, SAINT PAUL, MN, 55107
Intended purpose

A device intended to elevate the periosteum during orthopaedic surgery.

About this record

Access comprehensive regulatory information for Elevator, orthopaedic, periosteal in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 481887 and sponsored by Device Technologies Australia Pty Ltd, manufactured by Scanlan International in United States of America. The device registration started on March 06, 2025.

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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