Vascular Reconstruction Device - India CDSCO Medical Device Registration
Vascular Reconstruction Device is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000236_89ebc02df6d024249a3f673317b07013_7e017c93a8cfc3a6ae562cb166b38907. This device is marketed under the brand name Stent. 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.
Brand Name
Stent
License Holder
Johnson & Johnson Private LimitedDevice Class
Approving Authority
CDSCO
Product Information
The Enterprise 2 Vascular Reconstruction Device is intended for use with occlusive devices in the treatment of intracranial aneurysms
C-Section Kit
Brand: PROLENE*
Coronary Artery Bypass Graft
Brand: PROLENE*
Coronary Artery Bypass Graft
Brand: PROLENE*
NON-STERILE NON-ABSORBABLE SURGICAL SUTURE U.S.P.
Brand: BLACK BRAIDED SILK
Coronary Artery Bypass Graft(ETHICON* CABG KIT)
Brand: PROLENE*
NON ABSORBABLE SURGICAL SUTURE U. S. P.
Brand: PROLENE*
NON ABSORBABLE SURGICAL SUTURE U. S. P.
Brand: BLACK BRAIDED SILK
NON ABSORBABLE SURGICAL SUTURE U. S. P.
Brand: PROLENE*
ABHY-ADV KIT
Brand: PROLENE*
Hernia Kit
Brand: PROLENE*

