Albumin Test Reagent for Nanolab 200 Analyzer - India CDSCO Medical Device Registration

Albumin Test Reagent for Nanolab 200 Analyzer is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000037_f49680c6ef8142939a49b09105963f01_91099b01d3a58c4eaeebda5298ecac65. 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

Albumin Test Reagent for Nanolab 200 Analyzer

UID: MFG/IVD/2020/000037_f49680c6ef8142939a49b09105963f01_91099b01d3a58c4eaeebda5298ecac65

Brand Name

by UV method

License Holder

Trivitron Healthcare Pvt. Ltd

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

ClinReact SyPA Albumin Test Reagent (by UV method) for Nanolab 200 Analyzer is intended for the quantitative measurement of Albumin concentrations in serum or plasma samples specifically for use with Nanolab 200 analyser.,α-Amylase Test Reagent (by UV method) for Nanolab 200 Analyzer(by UV method)-ClinReact SyPA α-Amylase Test Reagent (by UV method) for Nanolab 200 Analyzer is intended for the quantitative measurement of α-Amylase concentrations in serum or plasma samples specifically for use with Nanolab 200 Analyzer