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COVID-19 In Vitro Diagnostic Devices and Test Methods Database

COVID-19 In Vitro Diagnostic Medical Device - detail

COVID-19 Neutralizing Antibody Detection Kit

Manufactured by New Gene (Hangzhou) Bioengineering Co. Ltd., China - www.new-gene.net/ 

Device identification number
2305
CE Marking
Yes
HSC common list (RAT)
×No
Format
Manual, Near POC / POC
Physical Support
Cassette, Lateral flow, Strip
Target type
Antibody
Specimen
ACD plasma, Peripheral blood, Plasma, Serum
Cross-reactivity (pathogens tested)
Adenovirus, Influenza A, Influenza A H1N1, Influenza A H3N2, Influenza A H5N1, Influenza B, Influenza B Victoria, Influenza B Yamagata, Mumps Virus (MuV), Mycoplasma Pneumoniae, Respiratory Syncytial V (RSV)
Lineages detected
B.1.1.7 (Alpha), B.1.351 (Beta), B.1.427 (Epsilon), B.1.429 (Epsilon), B.1.617.1 (Kappa), B.1.617.2 (Delta), B.1.617.3, P.1 (Gamma)
Commercial Status
Commercialised
Last Update
2022-08-24 09:08:01 CET
Comments
This product is intended for the qualitative detection of neutralizing antibodies for SARS-CoV-2 spike glycoproteins. The test results can help to identify individuals with an adaptive immune response to SARS-CoV-2, which is acquired from recent or prior infection or vaccination. The COVID-19 Neutralization Antibody Detection Kit should not be used to diagnose acute SARS-CoV-2 infection.
Assay Type
Immuno-Antibody
Reader Required
No
Subcategory
Sample collection device
Method
Immunoassay
Measurement
Quantitative
Time
20 minutes
Subclass
Neutralization Antibody (NAb)
LOD
1 AU
Calibration
Evaluated
Analysis of cross reactivity
Evaluated
False positives
0.84 % (1 out of 118)
False negatives
1.63 % (2 out of 122)
Precision
Evaluated
Accuracy
98.8 % ( (Antibody))
Reproducibility
Evaluated
Robustness
Evaluated
Clinical Sensitivity
98.4 % ( (Antibody))
Clinical Specificity
99.2 % ( (Antibody))
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