Mesh
- UID
- IMP/MD/2022/000017_710fdb6adb881b408116ef95335e1961_47d2b9f68c02581fc5c2a6530f7dfacc
- Device class
- Class C
- Brand name
- Ventralight ST Mesh
- License holder
- Becton Dickinson India Private Limited
- Approving authority
- CDSCO
- Product information
- Phasix ST Mesh is indicated for use in the reinforcement of soft tissue, where weakness exists, in procedures involving soft tissue repair, such as for the repair of hernias, including hiatal hernias
Mesh is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000017_710fdb6adb881b408116ef95335e1961_47d2b9f68c02581fc5c2a6530f7dfacc. This device is marketed under the brand name Ventralight ST Mesh. The license holder is Becton Dickinson India Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO.
This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.