CDSCO UID IMP/MD/2019/000225_59affb4d0c3082dbd602d4c89860e6d5_f958eaaf33c134d600efb85ede6d0806

Valve System

Edwards Lifesciences (India) Private Limited,·Device Class Class D·India CDSCO·Brand: Inspiris Resilia Aortic Valve
Registration details
UID
IMP/MD/2019/000225_59affb4d0c3082dbd602d4c89860e6d5_f958eaaf33c134d600efb85ede6d0806
Device class
Class D
Brand name
Inspiris Resilia Aortic Valve
Approving authority
CDSCO
Product information
The Valve is indicated for patients whose aortic valvular disease is sufficiently advanced to warrant replacement of their native valve with a prosthetic valve. These devices are also intended to use in patients with a previously implanted aortic valve that requires replacement. In the latter case, the previously implanted prosthesis is surgically excised and replaced with the model 8300AB valve
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About this record

Valve System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000225_59affb4d0c3082dbd602d4c89860e6d5_f958eaaf33c134d600efb85ede6d0806. This device is marketed under the brand name Inspiris Resilia Aortic Valve. The license holder is Edwards Lifesciences (India) Private Limited,, and it is classified as Device Class Class D. The approving authority is CDSCO.

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