Meniscal Repair System
- UID
- IMP/MD/2019/000335_f6899d34faf34550e361aff1bf7645c8_0426f0e2f3449f9301c92f68164936cf
- Device class
- Class D
- Brand name
- Healix Advance Knotless PEEK Anchor
- License holder
- Johnson & Johnson Private Limited
- Approving authority
- CDSCO
- Product information
- The OMNISPAN System is intended for use in the arthroscopic fixation of soft tissue procedures such as meniscal repair
Meniscal Repair System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000335_f6899d34faf34550e361aff1bf7645c8_0426f0e2f3449f9301c92f68164936cf. This device is marketed under the brand name Healix Advance Knotless PEEK Anchor. The license holder is Johnson & Johnson Private Limited, and it is classified as Device Class Class D. 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.