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Percutaneous Transluminal Coronary Angioplasty Balloon Catheter - India CDSCO Medical Device Registration

Percutaneous Transluminal Coronary Angioplasty Balloon Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000323_f8ede927a0a44c59b2d567265891d4eb_8596f4d359027751171532c68182265e. This device is marketed under the brand name PTCA. The license holder is M/s S3V Vascular Technologies Pvt. Limited, 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
Percutaneous Transluminal Coronary Angioplasty Balloon Catheter
UID: MFG/MD/2022/000323_f8ede927a0a44c59b2d567265891d4eb_8596f4d359027751171532c68182265e

Brand Name

PTCA

Device Class

Class D

Approving Authority

Sub Zonal Bangalore

Product Information

"The PTCA Balloon Dilatation Catheter is intended for use in the treatment of patients with clinical symptoms of myocardial ischemia related to the pathological condition of one or more coronary arteries."

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