Arterial Perfusion Cannula
- UID
- IMP/MD/2022/000042_72d4f59aaeb79412f9cc1e035bf7cc72_57c4d166071452670dde5e6e48f2f76b
- Device class
- Class D
- Brand name
- Fem-Flex II™ Femoral Arterial Cannula
- License holder
- Edwards Lifesciences (India) Private Limited,
- 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
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 II™ 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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