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Angioplasty PTCA Balloon Catheter - India CDSCO Medical Device Registration

Angioplasty PTCA Balloon Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2019/000029_6ae3f5754ad5e5986ec431b3ba90fb45_42ab1d44000a896d036432fcbab1ff50. This device is marketed under the brand name 3V SIRIS. The license holder is S3V Vascular Technologies Pvt Ltd, and it is classified as Device Class Class D. The approving authority is Sub Zonal Bangalore.

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 D
Angioplasty PTCA Balloon Catheter
UID: MFG/MD/2019/000029_6ae3f5754ad5e5986ec431b3ba90fb45_42ab1d44000a896d036432fcbab1ff50

Brand Name

3V SIRIS

Device Class

Class D

Approving Authority

Sub Zonal Bangalore

Product Information

Treatment of patients with clinical symptoms of Myocardial ischemia related to the pathological condition of one or more coronary arteries

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