Lilliput Extracorporeal Membrane Oxygenator(Lilliput 1 and Lilliput 2 )
- UID
- IMP/MD/2018/000439_71046f17cb49130c8b16c5ac324d2488_6441d2f583e6881846f9100f33d07b03
- Device class
- Class C
- Brand name
- DHF- Haemoconcentrator
- License holder
- LIVANOVA INDIA PVT. LTD.
- 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 patient’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
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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