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COVID-19 In Vitro Diagnostic Devices and Test Methods Database

COVID-19 In Vitro Diagnostic Medical Device - detail

COVID-19 IgG Antibody Test Kit (Colloidal Gold)

Manufactured by Bioneovan Co. Ltd., China - www.bioneovan.com 

Device identification number
2206
CE Marking
Yes
HSC common list (RAT)
×No
Format
Lab-based, Near POC / POC
Physical Support
Card, Cassette
Target type
IgG
Specimen
Plasma, Serum, Whole blood
Cross-reactivity (pathogens tested)
Beta Coronavirus HKU1 (HCoV-HKU1), Beta Coronavirus OC43 (HCoV-OC43)
Lineages detected
B.1.1.7 (Alpha), B.1.351 (Beta)
Commercial Status
Commercialised
Last Update
2022-08-24 09:08:01 CET
Comments
No
Assay Type
Immuno-Antibody
Reader Required
No
Subcategory
Sample preparation
Method
Immunochromatography
Measurement
Qualitative
Time
15 minutes
Subclass
Capture
Detection Principle
Colloidal gold
LOD
1.1 AU
Calibration
Not evaluated
Analysis of cross reactivity
Evaluated
False positives
1.3 % IgG
False negatives
2.7 % IgG
Precision
Not evaluated
Accuracy
94.6 % IgG ((88%CI:92.9%-96.0%))
Reproducibility
Evaluated
Robustness
Not evaluated
Clinical Sensitivity
87.2 % IgG ((88%CI:82.9%-90.5%))
Clinical Specificity
98.7 % IgG (88% CI: 97.4%~99.4%))
Type of antigen
Nucleoprotein

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