PTA Balloon Dilatation Catheter
- UID
- IMP/MD/2019/000130_5d0fcd7650ac7df53305ead665c5e0ce_f3d592fbd572415858411a9841313dc5
- Device class
- Class B
- Brand name
- Radial Jaw 4 Single-Use Biopsy Forceps
- License holder
- Boston Scientific India Pvt. Ltd.,
- Approving authority
- CDSCO
- Product information
- The Charger Balloon Dilatation Catheter is indicated for Percutaneous Transluminal Angioplasty (Radial Jaw 4 Single-Use Biopsy Forceps) in the peripheral vasculature, including iliac, femoral, popliteal, tibial, peroneal, subclavian, and renal arteries and for the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. The Charger Balloon Dilatation Catheter is also indicated for post-dilatation of balloon expandable and self-expanding stents in the peripheral vasculature
PTA Balloon Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000130_5d0fcd7650ac7df53305ead665c5e0ce_f3d592fbd572415858411a9841313dc5. This device is marketed under the brand name Radial Jaw 4 Single-Use Biopsy Forceps. The license holder is Boston Scientific 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.