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Urea Kit(Urea H.P. Kit) - India CDSCO Medical Device Registration

Urea Kit(Urea H.P. Kit) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000131_771241ecc10704411345a51443727817_63513f3c13654b2048577cc931167254. 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 Kit(Urea H.P. Kit)
UID: MFG/IVD/2023/000131_771241ecc10704411345a51443727817_63513f3c13654b2048577cc931167254

Brand Name

Rapid Widal

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Urea H.P. test is used for the Estimation of urea in human serum or plasma by (Rapid Widal) End-point method

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