Percutaneous Transluminal Angioplasty Balloon Dilatation Catheter
- UID
- IMP/MD/2022/000140_f38a95670092cb334e9bffcd87e3baef_d1cd88144ec68dcb398a3412d9539baf
- Device class
- Class C
- Brand name
- PALMAZ GENESIS®
- License holder
- Cardinal Health Medical Products India Pvt Ltd
- Approving authority
- CDSCO
- Product information
- The Cordis AVIATOR™ PLUS PTA Balloon Dilatation Catheter is indicated for Percutaneous Transluminal Angioplasty in the peripheral vasculature, including iliac, femoral, ilio-femoral, popliteal, infra popliteal, renal, and carotid arteries, and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. This device is also indicated for post-dilatation of balloon-expandable and self-expanding stents in the peripheral vasculature.
Percutaneous Transluminal Angioplasty Balloon Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000140_f38a95670092cb334e9bffcd87e3baef_d1cd88144ec68dcb398a3412d9539baf. This device is marketed under the brand name PALMAZ GENESIS®. The license holder is Cardinal Health Medical Products India Pvt Ltd, and it is classified as Device Class Class C. 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.