PTCA-Percutaneous Transluminal Coronary Angioplasty Catheter
- UID
- IMP/MD/2019/000385_4abba7cc35a5cca7d38f3541beb5ae1e_12e802b2ef29c41d9a004210f2ea9bfb
- Device class
- Class D
- Brand name
- VEGA
- License holder
- Nano Therapeutics Pvt. Ltd.
- Approving authority
- CDSCO
- Product information
- The Vega Catheter is intended for use in the treatment of patients with clinical symptoms of myocardial ischemia elated to the pathological condition of one or more coronary arteries. It is therefore indicated to dilate the diseased segment(VEGA) in a coronary artery or a coronary bypass, to improve myocardial perfusion
PTCA-Percutaneous Transluminal Coronary Angioplasty Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000385_4abba7cc35a5cca7d38f3541beb5ae1e_12e802b2ef29c41d9a004210f2ea9bfb. This device is marketed under the brand name VEGA. The license holder is Nano Therapeutics 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.