Coronary Stent System
- UID
- IMP/MD/2020/000134_0f0e5f038f5f9be051a98a006bceff3e_74ff44766c3fad29ae059f2eb5bf38d8
- Device class
- Class D
- Brand name
- Yukon Choice 4
- License holder
- Translumina Therapeutics LLP
- Approving authority
- CDSCO
- Product information
- The Yukon® Choice 4 stent system is indicated for intraluminal chronic placement in stenosed coronary artery or aorto-coronary bypass grafts or the tibial anterior and posterior artery of the lower limb with a maximum lesion length of 45 mm, 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
Coronary Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000134_0f0e5f038f5f9be051a98a006bceff3e_74ff44766c3fad29ae059f2eb5bf38d8. 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.