Dengue IgM ELISA - India CDSCO Medical Device Registration

Dengue IgM ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2018/000001_d717357c62a66962b29fe6b3023a302c_4ab390147f9347d89bbe60f4e2943dd4. This device is marketed under the brand name LiquiMAX, Lyphomax, Automax and other OEM Brands. The license holder is Avecon Healthcare Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is Haryana.

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CDSCO Registered

Class Class B

Dengue IgM ELISA

UID: MFG/IVD/2018/000001_d717357c62a66962b29fe6b3023a302c_4ab390147f9347d89bbe60f4e2943dd4

Brand Name

LiquiMAX, Lyphomax, Automax and other OEM Brands

License Holder

Avecon Healthcare Pvt. Ltd

Device Class

Class B

Approving Authority

Haryana

Product Information

DENGUE IgM ELISA is designed for in-vitro qualitative detection of Dengue IgM Antibodies in human serum or plasma and is used as a screening test for testing of collected blood samples suspected for DENGUE