Typhoid Antibody Test - India CDSCO Medical Device Registration

Typhoid Antibody Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000131_c6863c3b2f94d079f9849d45154ffa06_b51341a83bf04a1e79e459f2f8dcc11a. 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

Typhoid Antibody Test

UID: MFG/IVD/2023/000131_c6863c3b2f94d079f9849d45154ffa06_b51341a83bf04a1e79e459f2f8dcc11a

Brand Name

Rapid Widal

License Holder

BIOLAB DIAGNOSTICS (I) PVT. LTD.

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Rapid Typhoid IgG/IgM test is a lateral flow immunoassay for the detection and differentiation of anti-Salmonella typhi IgG and IgM in human serum or plasma

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Alkaline Phosphatase Kit(Alkaline Phosphatase Kit)

Brand: Rapid Widal

BIOLAB DIAGNOSTICS (I) PVT. LTD.

Typhoid Antibody Test - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

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Rheumatoid Arthritis Kit

Lipase(Lipase )

Creatinine FK

Total Protein(Total Protein )

Malaria Stain

Microprotein Kit

LDH Kit(LDH-L )