PCT/CRP Fast Test Kit (Immunofluorescence Assay)

Primary DI

06954414702064

Basic UDI-DI Code

B-06954414702064

Reference

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Device Types

Single use

Regulation

Eu Ivdd

Classification

Eu Ivd General

Status

On The Market

Manufacturer

Getein Biotech, Inc.

PCT/CRP Fast Test Kit (Immunofluorescence Assay) is intended for in vitro quantitative determination of Procalcitonin (PCT) and C-reactive protein (CRP) in serum, plasma or whole blood. The combination of CRP and PCT will be more accurately to determine the degree of infection and inflammation. It helps to identify systemic or local infection, bacterial infection or virus infection, determine the severity of infection and instruct clinical use of antibiotics. Therefore, the combination of PCT and CRP, when using a wider range of applications, more convenient and more accurate diagnosis. For professional use only.

Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).