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COVID-19 In Vitro Diagnostic Devices and Test Methods Database

COVID-19 In Vitro Diagnostic Medical Device - detail

fluorecare SARS-CoV-2 Antibody Test Kit (Fluorescence Immunoassay)

Manufactured by Shenzhen Microprofit Biotech Co. Ltd., China - www.microprofit-bio.com 

Device identification number
2182
CE Marking
Yes
HSC common list (RAT)
×No
Format
Manual
Physical Support
Cassette
Target type
Antibody
Specimen
Plasma, Serum
Lineages detected
B.1.1.7 (Alpha), B.1.351 (Beta)
Commercial Status
Commercialised
Last Update
2022-08-24 09:08:01 CET
Comments
www.microprofit-bio.com
Assay Type
Immuno-Antibody
Reader Required
Yes
Method
Immunochromatography
Measurement
Quantitative
Time
15 minutes
Detection Principle
Fluorescence
LOD
0.001 AU
Calibration
Evaluated
Analysis of cross reactivity
Evaluated
False positives
6 %
False negatives
0.3 %
Precision
Evaluated
Accuracy
99.13 % ( (97.48%~99.82%))
Reproducibility
Evaluated
Robustness
Evaluated
Clinical Sensitivity
93.33 % ((77.93%~99.18%))
Clinical Specificity
99.68 % ( (98.24%~99.99%))
Type of antigen
Other

The database contains publicly available In Vitro Diagnostic Medical Devices for COVID-19 and it is being updated periodically. Please note that additional performance (as retrieved from manufacturers web pages) is provided only for devices commercially available with CE-IVD mark. Acknowledgements