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LDH Reagent Test Kit - India CDSCO Medical Device Registration

LDH Reagent Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000015_a5f88fda33f8767a45d5be789cef5380_02281761ebd964448256910ae1c7fedb. The license holder is DiaSys Diagnostics India Private Limited, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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CDSCO Registered
Class Class B
LDH Reagent Test Kit
UID: MFG/IVD/2022/000015_a5f88fda33f8767a45d5be789cef5380_02281761ebd964448256910ae1c7fedb

Device Class

Class B

Approving Authority

Kokan Division

Product Information

Diagnostic reagent for in vitro quantitative determination of LDH in human serum on photometric analyzers

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