Rheumatoid Arthritis Kit - India CDSCO Medical Device Registration

Rheumatoid Arthritis Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000131_e270e779bcb7b165ae49afdfbb9dac31_add92aa170e822e294c251c60cf4c235. 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.

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CDSCO Registered

Class Class B

Rheumatoid Arthritis Kit

UID: MFG/IVD/2023/000131_e270e779bcb7b165ae49afdfbb9dac31_add92aa170e822e294c251c60cf4c235

Brand Name

Rapid Widal

License Holder

BIOLAB DIAGNOSTICS (I) PVT. LTD.

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Rapid RA is latex slide test for the qualitative determination of the Rhumatoid factor in Serum/Plasma

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Alkaline Phosphatase Kit(Alkaline Phosphatase Kit)

Brand: Rapid Widal

BIOLAB DIAGNOSTICS (I) PVT. LTD.

Rheumatoid Arthritis Kit - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

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Total Protein(Total Protein )

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Microprotein Kit

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