Fast Swab Covid-19 Antigen Rapid Test Kit Clinical Diagnosis Test

Certification:CE; ISO
Minimum Order Quantity:10-100pcs
Delivery Time:3-5working days
Place of Origin:Beijing
Price:USD1.8-3.5/pc
Supply Ability:1million per week
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Location: Wuxi Jiangsu China
Address: Huafa Mansion, Binhu District, Wuxi, Jiangsu Province, China
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CE Antigen Fast Diagnose Test for fresh swabs COVID-19 Antigen Rapid Test Kit Clinical Fast test

PERFORMANCE CHARACTERCS

The assay demonstrated excellent clinical specificity 100% (95% CI: 98.12%-100%). Overall Agreement was 96.21% (93.34%-97.87%).


Clinical Performance of Antigen Test for fresh swabs

Using 127 fresh NP swabs which were collected freshly in Extraction Buffer in the kit to evaluate the Clinical performance of the COVID-19 Antigen Rapid Test Kit. 67 Patients who presented within 7 days of symptom onset and 60 normal persons were included in the initial primary evaluation. The Result is below:


Sansure Covid-19 RT-PCR Assay
PositiveNegativeTotal
Kewei COVID-19 Antigen Rapid AssayPositive64064
Negative36063
Total6760127

The assay demonstrated acceptable clinical sensitivity for fresh swab samples is 95.52% (95% CI: 87.64%-98.47%) when compared to a molecular device produced by Sansure Inc. The assay demonstrated excellent clinical specificity 100% (95% CI: 93.98%-100%). Overall Agreement was 97.64% (93.28%-99.19%). The assay demonstrated acceptable total clinical sensitivity is 91.08% (95% CI: 85.59%-94.61%) when compared to a molecular device produced by Sansure Inc. The assay demonstrated excellent clinical specificity 100% (95% CI: 98.54%-100%). Overall Agreement was 96.64% (94.44%-97.99%).


1. Overall Clinical Performance of Antigen Test Kit

A total of above 157 positive samples and 260 negative samples were detected to evaluate the clinical performance of the COVID-19 Antigen Rapid Test Kit. The Result is below:

Sansure Covid-19 RT-PCR Assay
PositiveNegativeTotal
Kewei COVID-19 Antigen Rapid AssayPositive1430143
Negative14260274
Total157260417

The assay demonstrated acceptable total clinical sensitivity is 91.08% (95% CI: 85.59%-94.61%) when compared to a molecular device produced by Sansure Inc. The assay demonstrated excellent clinical specificity 100% (95% CI: 98.54%-100%). Overall Agreement was 96.64% (94.44%-97.99%).


2. Limit of Detection(LoD)


Limit of detection (LoD) was determined by evaluating different concentrations of heat inactivated SARS-CoV-2 virus. LoD of the SARS-CoV-2 antigen rapid kit was confirmed as 38.5 TCID50/ml.


3. High-dose Hook effect

No high dose hook effect was observed when test with up to a concentration of 6.3×105 TCID50/ml of heat inactive SARS-CoV-2 virus from Academy of Military Sciences PLA China.




China Fast Swab Covid-19 Antigen Rapid Test Kit Clinical Diagnosis Test supplier

Fast Swab Covid-19 Antigen Rapid Test Kit Clinical Diagnosis Test

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