Dengue IgM ELISA
- UID
- MFG/IVD/2018/000001_d717357c62a66962b29fe6b3023a302c_4ab390147f9347d89bbe60f4e2943dd4
- Device class
- Class B
- Brand name
- LiquiMAX, Lyphomax, Automax and other OEM Brands
- License holder
- Avecon Healthcare Pvt. Ltd
- 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
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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