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_63f055effa39cc497ec4a50ce6320851. 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.

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CDSCO Registered

Class Class D

Balloon Dilatation Catheter

UID: IMP/MD/2021/000004_16eb53f14e746dc332d80db12a830d7a_63f055effa39cc497ec4a50ce6320851

Brand Name

Artimes

License Holder

Veiva Scientific India Pvt. Ltd.

Device Class

Class D

Approving Authority

CDSCO

Product Information

The balloon dilatation catheter is intended for balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis for the purpose of improving myocardial perfusion, and also intended for balloon dilatation of a stent after implantation (Artimes).