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AST Reagent Test Kit - India CDSCO Medical Device Registration

AST Reagent Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000152_abcc9d259b2ae1f6852e60dd10c32de9_78ec9fadb4be1c698098d80bc992a3ef. This device is marketed under the brand name LDH. The license holder is M/s JITM C Genes Private Limited, and it is classified as Device Class Class B. The approving authority is Uttar Pradesh.

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
AST Reagent Test Kit
UID: MFG/IVD/2023/000152_abcc9d259b2ae1f6852e60dd10c32de9_78ec9fadb4be1c698098d80bc992a3ef

Brand Name

LDH

Device Class

Class B

Approving Authority

Uttar Pradesh

Product Information

Diagnostic reagent for in vitro quantitative determination of AST/SGOT in human serum or plasma on photometric analyzers

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