LDH-P Test Reagent Kit For Nanolab 500 Analyzer - India CDSCO Medical Device Registration

LDH-P Test Reagent Kit For Nanolab 500 Analyzer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000037_f21bc0924fa108698dbb98c6d482c008_666cc093ce30920143cc9d1428c907ae. This device is marketed under the brand name by UV method. The license holder is Trivitron Healthcare Pvt. Ltd, and it is classified as Device Class Class B. The approving authority is Tamil Nadu.

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CDSCO Registered

Class Class B

LDH-P Test Reagent Kit For Nanolab 500 Analyzer

UID: MFG/IVD/2020/000037_f21bc0924fa108698dbb98c6d482c008_666cc093ce30920143cc9d1428c907ae

Brand Name

by UV method

License Holder

Trivitron Healthcare Pvt. Ltd

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

ClinReact SyPA LDH-P Test Reagent Kit (by UV method) for Nanolab 500 Analyzer is intended for the quantitative measurement of Lactate Dehydrogenase (by UV method) concentration in serum or plasma samples specifically for use with Nanolab 500 Analyzer

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