Chikungunya Antibody test - India CDSCO Medical Device Registration

Chikungunya Antibody test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000131_1aa55ff929d4f386b2b8d923e91d49ab_d34359ac68de57cfea6897e71ae9d9a6. This device is marketed under the brand name Rapid Widal. The license holder is BIOLAB DIAGNOSTICS (I) PVT. LTD., and it is classified as Device Class Class B. The approving authority is Kokan Division.

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 B

Chikungunya Antibody test

UID: MFG/IVD/2023/000131_1aa55ff929d4f386b2b8d923e91d49ab_d34359ac68de57cfea6897e71ae9d9a6

Brand Name

Rapid Widal

License Holder

BIOLAB DIAGNOSTICS (I) PVT. LTD.

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Rapid Chikungunya IgM is a lateral flow immunoassay for the qualitative detection and Chromatographic immunoassay for the qualitative detection IgM anti-chikungunyain human serum, plasma and whole blood. It is intended to be used as a screening test and aid in the diagnosis of infection with Chikungunya

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Alkaline Phosphatase Kit(Alkaline Phosphatase Kit)

Brand: Rapid Widal

BIOLAB DIAGNOSTICS (I) PVT. LTD.

Chikungunya Antibody test - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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Amylase(Amylase )

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Rheumatoid Arthritis Kit

Lipase(Lipase )

Creatinine FK

Total Protein(Total Protein )

Typhoid Antibody Test

Malaria Stain

Microprotein Kit