Percutaneous Transluminal Angioplasty Balloon Dilatation Catheter
- UID
- IMP/MD/2022/000149_f38a95670092cb334e9bffcd87e3baef_097dac169504bf450848a2ba2cb931c1
- Device class
- Class B
- Brand name
- PTA
- License holder
- Cardinal Health Medical Products India Pvt Ltd
- Approving authority
- CDSCO
- Product information
- The POWERFLEX® PRO PTA catheter is intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal, infra popliteal and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. The device is also indicated for post-dilation 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/2022/000149_f38a95670092cb334e9bffcd87e3baef_097dac169504bf450848a2ba2cb931c1. This device is marketed under the brand name PTA. The license holder is Cardinal Health Medical Products India Pvt Ltd, and it is classified as Device Class Class B. 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.