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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.

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.

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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

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

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