ARTG 474971Clinical goniometer, manually-operated
ARTG ID: 474971 · Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes · DePuy Ireland UC · Class I · Started January 03, 2025
Good Name: Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes - Clinical goniometer, manually-operated
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- ARTG ID
- 474971
- Start Date
- January 03, 2025
- Effective Date
- January 03, 2025
- Name
- DePuy Ireland UC
- Country
- Ireland
- Address
- Loughbeg Ringaskiddy, Co Cork
A reusable manually-operated device that is used to measure the range of motion of the limb of a patient by measuring the angle of movement achieved at the joint.
Access comprehensive regulatory information for Clinical goniometer, manually-operated in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 474971 and sponsored by Johnson & Johnson Medical Pty Ltd t/a DePuy Synthes, manufactured by DePuy Ireland UC in Ireland. The device registration started on January 03, 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.