Diagnostics Rapid test reagent/ kits for Dengue COMBO - India CDSCO Medical Device Registration

Diagnostics Rapid test reagent/ kits for Dengue COMBO is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000064_32c396c6b99926493bab240edf8cd9e7_fb3c0a0712175401006c33d9407f0ab9. This device is marketed under the brand name Dry Fluorescence Immunoassay. The license holder is M/s Allied Biotechnology India Pvt Ltd, and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West Zone.

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CDSCO Registered

Class Class C

Diagnostics Rapid test reagent/ kits for Dengue COMBO

UID: MFG/IVD/2022/000064_32c396c6b99926493bab240edf8cd9e7_fb3c0a0712175401006c33d9407f0ab9

Brand Name

Dry Fluorescence Immunoassay

License Holder

M/s Allied Biotechnology India Pvt Ltd

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

Dengue Combo Test is a rapid immunochromatographic assay for the qualitative detection of dengue NS1 antigen and IgG and IgM antibodies in human Serum/Plasma Samples