Pure Global

Mesh - India CDSCO Medical Device Registration

Mesh is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000017_710fdb6adb881b408116ef95335e1961_1ff6ade5bd784748762222c8d0f7f07a. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
Mesh
UID: IMP/MD/2022/000017_710fdb6adb881b408116ef95335e1961_1ff6ade5bd784748762222c8d0f7f07a

Brand Name

Ventralight ST Mesh

Device Class

Class C

Approving Authority

CDSCO

Product Information

Ventralight ST Mesh is indicated for use in the reconstruction of soft tissue deficiencies, such as for the repair of hernias and chest wall defects. The Echo PS Positioning System is intended to be used to facilitate the delivery of soft tissue prostheses during laparoscopic hernia repair

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing