Carotid Artery Stent System - India CDSCO Medical Device Registration

Carotid Artery Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2021/000078_448ae1c2d6fa3f77339c3855cd566431_06622ed0fd500927eaf6279298561c9c. This device is marketed under the brand name Flow Re-Direction Endoluminal Device. The license holder is Faith Biotech 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

Carotid Artery Stent System

UID: IMP/MD/2021/000078_448ae1c2d6fa3f77339c3855cd566431_06622ed0fd500927eaf6279298561c9c

Brand Name

Flow Re-Direction Endoluminal Device

License Holder

Faith Biotech Pvt. Ltd.

Device Class

Class D

Approving Authority

CDSCO

Product Information

The CASPER Carotid Stent System is indicated for use in patients with carotid arterial atherosclerotic disease

Class D

Brand: Flow Re-Direction Endoluminal Device

Class D