Kewei COVID-19 total antibody ELISA Test Kit
Manufactured by Beijing Kewei Clinical Diagnostic Reagent Inc., China - en.keweidiagnostic.com/
Device identification number
1111
CE Marking
✓Yes
HSC common list (RAT)
×No
Format
Automated, Manual
Target type
Antibody
Specimen
Plasma, Serum
Commercial Status
Commercialised
Last Update
2022-08-24 09:08:01 CET
Comments
http://en.keweidiagnostic.com/index.php?m=content&c=index&a=show&catid=199&id=175
Assay Type
Immuno-Antibody
Rapid Diagnostic
No
Reader Required
Yes
Method
ELISA
Measurement
Qualitative
Time
60 minutes
Subclass
Sandwich, Double
Accuracy
96 %
Clinical Sensitivity
94.71 %
Clinical Specificity
99.6 %
Notes
Manual or automated microtiter plate Sandwich, Double
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