Nitinol Stent System
- UID
- IMP/MD/2022/000230_d3f45bd0320504207a059bd641665ff3_88fe93e167abf9fb2c8e9108ad229b44
- Device class
- Class D
- Brand name
- OPTEASE®
- License holder
- Cardinal Health Medical Products India Pvt Ltd
- Approving authority
- CDSCO
- Product information
- The Cordis PRECISE® PRO Rx Nitinol Stent System is indicated for use in patients with stenotic lesions of the carotid artery(OPTEASE®)
Nitinol Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2022/000230_d3f45bd0320504207a059bd641665ff3_88fe93e167abf9fb2c8e9108ad229b44. This device is marketed under the brand name OPTEASE®. The license holder is Cardinal Health Medical Products India Pvt Ltd, and it is classified as Device Class Class D. The approving authority is CDSCO.
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