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Urea Berthelot Test Kit - India CDSCO Medical Device Registration

Urea Berthelot Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000134_7e1e382102e931345665c229628c2a53_0e0300d9240c41fcc1b68c0246114d71. The license holder is DiaSys Diagnostics India Private Limited, 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 Berthelot Test Kit
UID: MFG/IVD/2023/000134_7e1e382102e931345665c229628c2a53_0e0300d9240c41fcc1b68c0246114d71

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Diagnostic reagent for quantitative determination of Urea in human serum or plasma on photometric analyzers

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