Fascial tissue dilator, single-use
Australia TGA ARTG Registered Device · William A Cook Australia Pty Ltd · Cook Vandergrift Inc · Class IIa · Started September 24, 2021
Good Name: William A Cook Australia Pty Ltd - Fascial tissue dilator, single-use
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- September 24, 2021
- Effective Date
- September 24, 2021
- Country
- United States of America
- Address
- 1186 Montgomery Lane, Vandergrift, Pennsylvania, 15690
The Curved Inner Femoral Sheath is intended for use in patients requiring the percutaneous retrieval of indwelling catheters, cardiac leads, fragments of catheter tubing or wire guides and other foreign objects.
Access comprehensive regulatory information for Fascial tissue dilator, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by William A Cook Australia Pty Ltd, manufactured by Cook Vandergrift Inc in United States of America. The device registration started on September 24, 2021.
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.