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Balloon Peripheral Angioplasty Catheter - India CDSCO Medical Device Registration

Balloon Peripheral Angioplasty Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000129_03730532770d4b3c09e23cb5c886d05c_be290bc0aa82f1cacd73a5a67142b5d3. This device is marketed under the brand name XXL Esophageal Balloon Dilatation Catheter. 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.

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CDSCO Registered
Class Class B
Balloon Peripheral Angioplasty Catheter
UID: IMP/MD/2018/000129_03730532770d4b3c09e23cb5c886d05c_be290bc0aa82f1cacd73a5a67142b5d3

Brand Name

XXL Esophageal Balloon Dilatation Catheter

Device Class

Class B

Approving Authority

CDSCO

Product Information

XXL Balloon Dilatation Catheters are indicated for percutaneous transluminal angioplasty of narrowed segments in the Iliac arteries in the peripheral vasculature. XXL Balloon Dilatation Catheters are not indicated for use in coronary arteries nor in the neurovasculature

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