Peripheral angioplasty balloon catheter, basic
- UID
- IMP/MD/2019/000130_ad385d73974b2f5492610e9320f0ee13_89f7051db8533a51ceb8ac5be47de124
- 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 Mustang 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 Mustang Balloon Dilatation Catheter is also indicated for post-dilatation of balloon expandable and self-expanding stents in the peripheral vasculature. Mustang Balloon Dilatation Catheters with balloons up to 120 mm in length are indicated for the treatment of biliary strictures.
Peripheral angioplasty balloon catheter, basic is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000130_ad385d73974b2f5492610e9320f0ee13_89f7051db8533a51ceb8ac5be47de124. 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.
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