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COVID-19 In Vitro Diagnostic Devices and Test Methods Database

COVID-19 In Vitro Diagnostic Medical Device - detail

Novel Coronavirus (SARS-Cov-2) Antigen Rapid Test Cassette (swab)

Manufactured by Innovation Biotech(Beijing) Co. Ltd., China - www.invbio.com 

Device identification number
2278
CE Marking
Yes
HSC common list (RAT)
Yes
Format
Near POC / POC
Physical Support
Cassette
Target type
Antigen
Targets
nucleocapsid protein
Specimen
Nasal swab
Cross-reactivity (pathogens tested)
Alpha Coronavirus 229E (HCoV-229E), Alpha Coronavirus Nl63 (HCoV-Nl63), Beta Coronavirus HKU1 (HCoV-HKU1), Beta Coronavirus OC43 (HCoV-OC43), Coronaviruses (HCoV), Human Metapneumovirus (HMPV), Parainfluenza Virus Type 1, Parainfluenza Virus Type 2, Parainfluenza Virus Type 3, Parainfluenza Virus Type 4
Lineages detected
B.1.1.7 (Alpha), B.1.351 (Beta), P.1 (Gamma)
Commercial Status
Commercialised
Last Update
2022-08-24 09:08:01 CET
Comments
The Novel Coronavirus (SARS-Cov-2) Antigen Rapid Test Cassette (swab) is a rapid chromatographic immunoassay for the qualitative detection of N protein antigens to SARS-CoV-2 present in nasal swab . This test is for professional used only, as an aid to early diagnosis of SARS-CoV-2 infection in patient. The result of this test should not be the sole basis for the diagnosis; confirmatory testing is required
Assay Type
Immuno-Antigen
Rapid Diagnostic
Yes
Method
Immunochromatography
Time
15 minutes
Subclass
Sandwich, Double
LOD
1 AU
Calibration
Evaluated
Analysis of cross reactivity
Evaluated
False positives
5.26 AU
False negatives
1 AU
Precision
Evaluated
Accuracy
98.21 %
Reproducibility
Evaluated
Robustness
Evaluated
Clinical Sensitivity
95.6 %
Clinical Specificity
100 %
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