Arterial Perfusion Cannula - India CDSCO Medical Device Registration

Arterial Perfusion Cannula is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000111_72d4f59aaeb79412f9cc1e035bf7cc72_57c4d166071452670dde5e6e48f2f76b. This device is marketed under the brand name OptiSite Arterial Perfusion Cannula. 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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CDSCO Registered

Class Class D

Arterial Perfusion Cannula

UID: IMP/MD/2018/000111_72d4f59aaeb79412f9cc1e035bf7cc72_57c4d166071452670dde5e6e48f2f76b

Brand Name

OptiSite Arterial Perfusion Cannula

License Holder

Edwards Lifesciences (India) Private Limited,

Device Class

Class D

Approving Authority

CDSCO

Product Information

The Edwards Lifesciences arterial perfusion cannulae are indicated for arterial perfusion in the extracorporeal circuit for less than 6 hours. Cannulation site selection is left to the discretion of the surgeon and may include the femoral artery or the aortic arch. Extracorporeal circuit components with a Duraflo treatment are intended for use in cardiopulmonary bypass when a heparin treated cannula is desired upon initial placement