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Lilliput Extracorporeal Membrane Oxygenator(Dideco D901 Lilliput 1 and Dideco 902 Lilliput 2 ) - India CDSCO Medical Device Registration

Lilliput Extracorporeal Membrane Oxygenator(Dideco D901 Lilliput 1 and Dideco 902 Lilliput 2 ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000439_279216160fed4eaa94e43ee7088c7740_6207c3484be97b37a626b0ba7d6bb7b0. 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(Dideco D901 Lilliput 1 and Dideco 902 Lilliput 2 )
UID: IMP/MD/2018/000439_279216160fed4eaa94e43ee7088c7740_6207c3484be97b37a626b0ba7d6bb7b0

Brand Name

DHF- Haemoconcentrator

Device Class

Class C

Approving Authority

CDSCO

Product Information

Lilliput D901: It is intended for use in cardiopulmonary bypass circuits as a device to replace the function of the lungs in order to control the arterial/venous temperature and as a venous blood reservoir. It is indicated for use in procedures on patient with a body weight of less than 8 kg (DHF- Haemoconcentrator). The device should not be used longer than 6 hours. Lilliput D902: It is intended for use in infants not exceeding 20 kg (DHF- Haemoconcentrator) who undergo cardiopulmonary bypass surgery requiring extracorporeal circulation. It provides oxygenation and carbon dioxide removal from venous blood. The device should not be used longer than 6 hours

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