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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 MFG/MD/2021/000368_a30ff1f1f11823fa1792c61d531ea934_ca1b628251acff38be7dabe1e8ea0bcd. This device is marketed under the brand name Endorser, Patron, Hotron, Flextron. The license holder is Veritas Bioventions Pvt. Ltd, and it is classified as Device Class Class D. The approving authority is Central Drug Standards Control Organization, Ahmedabad.

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: MFG/MD/2021/000368_a30ff1f1f11823fa1792c61d531ea934_ca1b628251acff38be7dabe1e8ea0bcd

Brand Name

Endorser, Patron, Hotron, Flextron

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

The 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 2.00 mm to 4.50 mm and is intended to improve coronary luminal diameter

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