Pure Global

Balloon Expandable Coronary Stent System - Cobalt Chromium (Prozeta - Balloon Expandable Coronary Stent System - Cobalt Chromium ) - India CDSCO Medical Device Registration

Balloon Expandable Coronary Stent System - Cobalt Chromium (Prozeta - Balloon Expandable Coronary Stent System - Cobalt Chromium ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000521_f0c353ec806c4b55b3fa1b282fea6c3c_3e94fec6e3b556fdf19a066cf4e9f19b. This device is marketed under the brand name Cobalt Chromium. The license holder is Vascular Concepts 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class D
Balloon Expandable Coronary Stent System - Cobalt Chromium (Prozeta - Balloon Expandable Coronary Stent System - Cobalt Chromium )
UID: IMP/MD/2019/000521_f0c353ec806c4b55b3fa1b282fea6c3c_3e94fec6e3b556fdf19a066cf4e9f19b

Brand Name

Cobalt Chromium

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Prozeta Coronary Stent System is indicated for use in patients with symptomatic ischemic heart disease due to discrete de novo coronary artery lesions with a reference vessel diameter ranging from 2.0mm to 4.0mm (Cobalt Chromium) and is intended for treatment of coronary arteries

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing