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Cobalt Chromium Coronary Stent System - India CDSCO Medical Device Registration

Cobalt Chromium Coronary Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000564_480c36db004746cd8625cbc9ff462bd9_f5f3526e56091e838e9631dde5e73ffe. This device is marketed under the brand name CYGNUS II. The license holder is Envision Scientific Pvt. Ltd., 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.

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CDSCO Registered
Class Class D
Cobalt Chromium Coronary Stent System
UID: IMP/MD/2021/000564_480c36db004746cd8625cbc9ff462bd9_f5f3526e56091e838e9631dde5e73ffe

Brand Name

CYGNUS II

Device Class

Class D

Approving Authority

CDSCO

Product Information

It is intended for use in the treatment of patients with clinical symptoms of myocardial ischemia related to the pathological conditions of one or more coronary arteries. Recognized use of intracoronary stents currently include but is not limited to the treatment of de novo or restenostic lesions in native coronary arteries and in de novo lesions of saphenous vein grafts. CYGNUS III is available for intracoronary implantation for inner vessel diameters of 2.25 to 5.00 mm

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