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Peripheral angioplasty balloon catheter, basic - India CDSCO Medical Device Registration

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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CDSCO Registered
Class Class B
Peripheral angioplasty balloon catheter, basic
UID: IMP/MD/2019/000130_ad385d73974b2f5492610e9320f0ee13_89f7051db8533a51ceb8ac5be47de124

Brand Name

Radial Jaw 4 Single-Use Biopsy Forceps

Device Class

Class B

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.

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