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Polymer free Hydroxyapatite coated Sirolimus Eluting Coronary Stent System - India CDSCO Medical Device Registration

Polymer free Hydroxyapatite coated Sirolimus Eluting Coronary Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000008_6fe54519b39bd65e1cbb3277b234f344_29a838d528b5e8cccd9e594da3d7816b. This device is marketed under the brand name Vestasync Sirolimus Eluting Coronary Stent System. The license holder is PURPLE MICROPORT CARDIOVASCULAR PRIVATE LIMITED, 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
Polymer free Hydroxyapatite coated Sirolimus Eluting Coronary Stent System
UID: MFG/MD/2019/000008_6fe54519b39bd65e1cbb3277b234f344_29a838d528b5e8cccd9e594da3d7816b

Brand Name

Vestasync Sirolimus Eluting Coronary Stent System

Device Class

Class D

Approving Authority

Central Drug Standards Control Organization, Ahmedabad

Product Information

Product is indicated for improving coronary luminal diameter in patients with symptomatic ischemic heart disease in de novo coronary artery lesion in native coronary arteries in patients eligible for percutaneous Transluminal Coronary Angioplasty (Vestasync Sirolimus Eluting Coronary Stent System)

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DJ Fang

DJ Fang

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