Chikungunya IgG/Igm Rapid Test - India CDSCO Medical Device Registration

Chikungunya IgG/Igm Rapid Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000109_b238930cf8812b7a8d66813e2adef8c7_63275b76d70dbf12ce4b4c0fe7048a5e. This device is marketed under the brand name 3 Parameters. The license holder is Biotrol Laboratories Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is West Delhi Division.

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CDSCO Registered

Class Class B

Chikungunya IgG/Igm Rapid Test

UID: MFG/IVD/2021/000109_b238930cf8812b7a8d66813e2adef8c7_63275b76d70dbf12ce4b4c0fe7048a5e

Brand Name

3 Parameters

License Holder

Biotrol Laboratories Pvt. Ltd.

Device Class

Class B

Approving Authority

West Delhi Division

Product Information

The Chikungunya IgG/IgM Rapid Test is lateral flow chromatographic immunoassay for the qualitative detection of IgG/IgM anti-chikungunya virus (3 Parameters) in human serum, plasma or whole blood. It is intended to be used as screening test and as an aid in the diagnosis of infection with CHK. Any reactive specimen with the chikunguniya IgG/IgM rapid test must be confirmed with alternative testing method and clinical findings

Class B

HSV IgG/Igm Rapid Test

Brand: 3 Parameters

Biotrol Laboratories Pvt. Ltd.

Class B

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Chikungunya IgG/Igm Rapid Test - India CDSCO Medical Device Registration

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