Urea (Urea ) - India CDSCO Medical Device Registration

Urea (Urea ) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000131_7653796960792e61cf1b30218d02723a_cbccb5dba09f29f6ff3b97195290556e. 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

Urea (Urea )

UID: MFG/IVD/2023/000131_7653796960792e61cf1b30218d02723a_cbccb5dba09f29f6ff3b97195290556e

Brand Name

Rapid Widal

License Holder

BIOLAB DIAGNOSTICS (I) PVT. LTD.

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Urea GLDH kit is used for the estimation of Urea and BUN in human serum or plasma

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Alkaline Phosphatase Kit(Alkaline Phosphatase Kit)

Brand: Rapid Widal

BIOLAB DIAGNOSTICS (I) PVT. LTD.

Urea (Urea ) - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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Alkaline Phosphatase Kit(Alkaline Phosphatase Kit)

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Alkaline Phosphatase Kit(Alkaline Phosphatase Kit)

Amylase(Amylase )

Cholesterol Total & HDL(Cholesterol Total & HDL )

Rheumatoid Arthritis Kit

Lipase(Lipase )

Creatinine FK

Total Protein(Total Protein )

Typhoid Antibody Test

Malaria Stain

Microprotein Kit