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COVID-19 In Vitro Diagnostic Devices and Test Methods Database

COVID-19 In Vitro Diagnostic Medical Device - detail

Rapid New Coronavirus (COVID19) Neutralizing Antibody Test

Manufactured by Immunospark s.r.l., Italy - www.immunospark.com 

Device identification number
1904
CE Marking
Yes
HSC common list (RAT)
×No
Format
Manual, Near POC / POC
Physical Support
Cassette
Target type
Antibody
Specimen
Peripheral blood, Plasma, Serum, Whole blood
Commercial Status
Commercialised
Last Update
2022-08-24 09:08:01 CET
Comments
competitive assay that provide a multiple interpretatino of the protection level
Assay Type
Immuno-Antibody
Reader Required
No
Subcategory
Other ()
Method
Immunochromatography
Measurement
Qualitative
Time
10 minutes
Subclass
Neutralization Antibody (NAb)
LOD
40 AU
Calibration
Evaluated
Analysis of cross reactivity
Evaluated
False positives
A smal amount of results did not correltaed with the reference but correlated with rapid test
False negatives
A smal amount of results did not correltaed with the reference but correlated with rapid test
Precision
Evaluated
Accuracy
99 %
Reproducibility
Evaluated
Robustness
Evaluated
Clinical Sensitivity
93 %
Clinical Specificity
99 %
Type of antigen
Other
Notes
Colloidal Gold detection

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