PTA Balloon Dilatation Catheter - India CDSCO Medical Device Registration
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.
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Brand Name
Radial Jaw 4 Single-Use Biopsy Forceps
License Holder
Boston Scientific India Pvt. Ltd.,Device Class
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
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