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Lilliput Extracorporeal Membrane Oxygenator(Lilliput 1 and Lilliput 2 ) - India CDSCO Medical Device Registration

Lilliput Extracorporeal Membrane Oxygenator(Lilliput 1 and Lilliput 2 ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000439_71046f17cb49130c8b16c5ac324d2488_6441d2f583e6881846f9100f33d07b03. This device is marketed under the brand name DHF- Haemoconcentrator. The license holder is LIVANOVA INDIA PVT. LTD., and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered
Class Class C
Lilliput Extracorporeal Membrane Oxygenator(Lilliput 1 and Lilliput 2 )
UID: IMP/MD/2018/000439_71046f17cb49130c8b16c5ac324d2488_6441d2f583e6881846f9100f33d07b03

Brand Name

DHF- Haemoconcentrator

Device Class

Class C

Approving Authority

CDSCO

Product Information

The Lilliput Oxygenators are extracorporeal circulations devices used to replace the patient respiratory function during cardiopulmonary bypass procedures. They are used in an extracorporeal perfusion circuit to oxygenate and remove carbon dioxide from the blood, and to cool or warm the blood during cardiopulmonary bypass procedures. The lilliput hard-shell venous reservoirs are extracorporeal circulation devices allowing oxygenators to exploit gas exchange function of patient lungs during cardiopulmonary bypass procedures, providing dynamic patientโ€™s venous blood collection. They also defoam and filter venous blood and suction blood through a filtering system made of antifoam agent and filter screen. The lilliput devices must be used up to 6 hours or less

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