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Coronary Stent System - India CDSCO Medical Device Registration

Coronary Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000134_0f0e5f038f5f9be051a98a006bceff3e_0a42fe6128753b4c9a02a6dd28391025. This device is marketed under the brand name Yukon Choice 4. The license holder is Translumina Therapeutics LLP, 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
Coronary Stent System
UID: IMP/MD/2020/000134_0f0e5f038f5f9be051a98a006bceff3e_0a42fe6128753b4c9a02a6dd28391025

Brand Name

Yukon Choice 4

Device Class

Class D

Approving Authority

CDSCO

Product Information

The YUKON CC Stent System is indicated for intraluminal chronic placement in stenosed coronary artery or aortocoronary bypass grafts or the tibial anterior and posterior artery of the lower limb with a maximum lesion length of 45mm, in order to obtain vessel patency following acute or subacute artery obstruction. It is also indicated in restenosis or arterial dissection after PTCA procedures. Patients being considered for stent implantation should be acceptable candidates for balloon angioplasty

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