Nitinol Stent System - India CDSCO Medical Device Registration
Nitinol Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000230_d3f45bd0320504207a059bd641665ff3_7c02596b335988dff54621e329adbdf4. This device is marketed under the brand name S.M.A.R.T.® CONTROL®. The license holder is Cardinal Health Medical Products India Pvt Ltd, and it is classified as Device Class Class C. 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.
Brand Name
S.M.A.R.T.® CONTROL®
License Holder
Cardinal Health Medical Products India Pvt LtdDevice Class
Approving Authority
CDSCO
Product Information
The Cordis S.M.A.R.T.® CONTROL® Nitinol Stent System is indicated for use in patients with atherosclerotic disease of peripheral arteries, including iliac and superficial femoral arteries.
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