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/2022/000042_72d4f59aaeb79412f9cc1e035bf7cc72_57c4d166071452670dde5e6e48f2f76b. This device is marketed under the brand name Fem-Flex IIโข Femoral Arterial 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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Brand Name
Fem-Flex IIโข Femoral Arterial Cannula
License Holder
Edwards Lifesciences (India) Private Limited,Device Class
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
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