Lilliput Extracorporeal Membrane Oxygenator
- UID
- IMP/MD/2018/000439_1eea6503cba0e60cba764705e0814182_ec2eba0389a525ca565778097f70f314
- Device class
- Class C
- Brand name
- DHF- Haemoconcentrator
- License holder
- LIVANOVA INDIA PVT. LTD.
- Approving authority
- CDSCO
- Product information
- The Lilliput 2 Ecmo Oxygenator is extracorporeal circulations device used to partially or fully support the patient respiratory function during extended respiratory support application oxygenating and removing carbon dioxide from the blood. The device is used to maintain or restore normothermic blood temperature. Lilliput 2 Ecmo oxygenator is intended to be used for 5 days or less
Lilliput Extracorporeal Membrane Oxygenator is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000439_1eea6503cba0e60cba764705e0814182_ec2eba0389a525ca565778097f70f314. 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.
This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.