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Balloon Dilatation Catheter - India CDSCO Medical Device Registration

Balloon Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000004_16eb53f14e746dc332d80db12a830d7a_38a9fea0d3c95ac8b33afb0f28c0e7a9. This device is marketed under the brand name Artimes. The license holder is Veiva Scientific India Pvt. Ltd., and it is classified as Device Class Class D. 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 D
Balloon Dilatation Catheter
UID: IMP/MD/2021/000004_16eb53f14e746dc332d80db12a830d7a_38a9fea0d3c95ac8b33afb0f28c0e7a9

Brand Name

Artimes

Device Class

Class D

Approving Authority

CDSCO

Product Information

The balloon dilatation catheter is indicated for balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis for the purpose of improving myocardial perfusion

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