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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/2018/000129_ad385d73974b2f5492610e9320f0ee13_84e0ac4a27db2a85fd4b8aab2811cbd3. This device is marketed under the brand name Hot Axios Stent and Electrocautery-Enhanced Delivery System. The license holder is Boston Scientific India Pvt. Ltd.,, and it is classified as Device Class Class C. 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.

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CDSCO Registered
Class Class C
Peripheral angioplasty balloon catheter, basic
UID: IMP/MD/2018/000129_ad385d73974b2f5492610e9320f0ee13_84e0ac4a27db2a85fd4b8aab2811cbd3

Brand Name

Hot Axios Stent and Electrocautery-Enhanced Delivery System

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Athletis PTA Balloon Dilatation Catheter is indicated for Percutaneous Transluminal Angioplasty in the peripheral vasculature including upper extremity, renal, iliac, and infrainguinal vessels and the treatment of obstructive lesions of native or synthetic arteriovenous dialysis fistulae. The Athletis PTA Balloon Dilatation Catheter is also indicated for postยญdilatation of stents and stent grafts in the peripheral vasculature

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