Eu Ivdd Eu Ivd General On The Market 🇨🇳 China

SARS-CoV-2 IgG Antibody Test Kit (Fluorescence immunochromatography)

Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0

Basic Information

Primary DI
06970877682019
Basic UDI-DI Code
B-06970877682019
Reference
0201
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

This kit is used for quantitative determination of IgG antibody content of new coronavirus (2019 nCoV) in human serum, plasma and whole blood samples in vitro. By detecting the content of IgG antibody against the new coronavirus (2019 nCoV) in the sample, it can be used as an auxiliary means to judge whether there is virus infection experience in the body and the immune response ability of the body to the new coronavirus (2019 nCoV) after virus infection, and can be used as an auxiliary basis to determine the vaccine injection demand.

CND Nomenclature Codes

Code Description
W01021699 RAPID TESTS & POINT OF CARE - IMMUNOCHEMISTRY - OTHER

Similar Devices

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

View all