Pure Global AI
CDSCO UID MFG/IVD/2023/000134_9eba7df9a942c66303eac660c71e22e2_0e0300d9240c41fcc1b68c0246114d71

Urea reagent test kit

DiaSys Diagnostics India Private LimitedDevice Class Class BIndia CDSCO
VerifiedCDSCO · official registry
Registration details
UID
MFG/IVD/2023/000134_9eba7df9a942c66303eac660c71e22e2_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
About this record

Urea reagent test kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000134_9eba7df9a942c66303eac660c71e22e2_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 the facts attached to this CDSCO registry row. Other records from the same license holder are available through the database search link without adding aggregation queries to this page. 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.