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C-Reactive Protein Test Reagent kit for Nanolab 500 Analyzer - India CDSCO Medical Device Registration

C-Reactive Protein 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/2020/000053_72dd74017862a0e1c26b802dc3947007_549799dfe6f318346d069a7bc164306d. This device is marketed under the brand name Immunoreactive Tripsinogen. The license holder is Trivitron Healthcare Pvt. Ltd, and it is classified as Device Class Class C. The approving authority is Central Drug Standard Control Organisation, South Zone.

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 C
C-Reactive Protein Test Reagent kit for Nanolab 500 Analyzer
UID: MFG/IVD/2020/000053_72dd74017862a0e1c26b802dc3947007_549799dfe6f318346d069a7bc164306d

Brand Name

Immunoreactive Tripsinogen

Device Class

Class C

Approving Authority

Central Drug Standard Control Organisation, South Zone

Product Information

ClinReact SyPA C-Reactive Protein Test Reagent kit (Immunoreactive Tripsinogen) for Nanolab 500 Analyzer is intended for the quantitative determination of Creactive protein (Immunoreactive Tripsinogen) in human serum or plasma, specifically for use with Nanolab 500 Analyser

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DJ Fang

DJ Fang

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