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One step rapid test kit for differential detection of Chikungunya IgM & IgG Ab - India CDSCO Medical Device Registration

One step rapid test kit for differential detection of Chikungunya IgM & IgG Ab is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000017_fbf3c3a389890566d27f2508a34dc507_e4ddabea46669b3e55afc686a3180019. This device is marketed under the brand name Standard F TSH FIA. The license holder is SD Biosensor 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
One step rapid test kit for differential detection of Chikungunya IgM & IgG Ab
UID: MFG/IVD/2020/000017_fbf3c3a389890566d27f2508a34dc507_e4ddabea46669b3e55afc686a3180019

Brand Name

Standard F TSH FIA

Device Class

Class B

Approving Authority

Haryana

Product Information

It is an immunochromatographic assay for the detection of IgM/IgG antibodies against Chikungunya virus in human serum, plasma or whole blood specimen

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