Australia TGA ARTG recordEndoscope accessory, filter, laser
Australia TGA ARTG Registered Device · Beaver-Visitec International Australia Pty Ltd · Beaver-Visitec International Inc · Class I · Started March 28, 2022
Good Name: Beaver-Visitec International Australia Pty Ltd - Endoscope accessory, filter, laser
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- March 28, 2022
- Effective Date
- March 28, 2022
- Country
- United States of America
- Address
- 39 Sycamore Avenue, LITTLE SILVER, NEW JERSEY, 07739
Medical device intended to filter the laser light produced by an endoscopy system so it is not visible.
Access comprehensive regulatory information for Endoscope accessory, filter, laser in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Beaver-Visitec International Australia Pty Ltd, manufactured by Beaver-Visitec International Inc in United States of America. The device registration started on March 28, 2022.
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.