Pure Global

PEEK ANCHOR WITH SUTURE - India CDSCO Medical Device Registration

PEEK ANCHOR WITH SUTURE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000003_7564abda3f76a900438768c9a272f2fc_fc99e49ec58efc6dbddf510d18c06f9a. This device is marketed under the brand name HEALIX ADVANCE BR ANCHOR WITH DYNACORD SUTURE. The license holder is Johnson & Johnson 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
PEEK ANCHOR WITH SUTURE
UID: IMP/MD/2019/000003_7564abda3f76a900438768c9a272f2fc_fc99e49ec58efc6dbddf510d18c06f9a

Brand Name

HEALIX ADVANCE BR ANCHOR WITH DYNACORD SUTURE

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Healix Advance Anchor is indicated in soft-tissue to bone fixation in association with post-operative immobilization as follows: Shoulder- Rotator Cuff Repair, Bankart Repair, SLAP Lesion Repair, Biceps Tenodesis, Acromioclavicular Separation Repair, Deltoid Repair, Capsular Shift or Capsulolabral Reconstruction; Foot/Ankle- Lateral Stabilization, Medial Stabilization, Achilles Tendon Repair; Knee- Medial Collateral Ligament Repair, Lateral Collateral Ligament Repair, Posterior Oblique, Ligament Repair, Iliotibial Band Tenodesis; Elbow- Biceps Tendon Reattachment, Ulnar Collateral Ligament Reconstruction, Radial Collateral Ligament Reconstruction; Hip- Capsular Repair, Acetabular Labral Repair

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing