SARS-COV-2/Influenza A&B Rapid Antigen Test
Manufactured by Joinstar Biomedical Technology Co. Ltd., China - www.joinstar.cn
Device identification number
1777
CE Marking
✓Yes
HSC common list (RAT)
×No
Format
Manual
Physical Support
Lateral flow
Target type
Antigen
Specimen
Nasal swab
Commercial Status
Commercialised
Last Update
2022-08-24 09:08:01 CET
Assay Type
Immuno-Antigen
Rapid Diagnostic
Yes
Reader Required
No
Method
Immunochromatography
Measurement
Qualitative
Time
15 minutes
Detection Principle
Colorimetry
LOD
0 U/ml
Calibration
Not evaluated
Analysis of cross reactivity
Evaluated
False positives
3 %
False negatives
1 %
Precision
Evaluated
Accuracy
98.9 %
Reproducibility
Evaluated
Robustness
Evaluated
Clinical Sensitivity
97.1 %
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