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Hangzhou Aichek Medical Technology Co.,Ltd
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OEM 25 Packs Neutralizing Antibody Rapid Test 96.6% Accuracy

Hangzhou Aichek Medical Technology Co.,Ltd
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OEM 25 Packs Neutralizing Antibody Rapid Test 96.6% Accuracy

Brand Name : Aichek

Model Number : COVID-19-G02001A

Certification : CE

Place of Origin : China

MOQ : 5000 Test

Price : negotiable

Payment Terms : T/T

Supply Ability : negotiable

Packaging Details : 40box/carton

Storage : 2℃-30℃

User : Everyone

Accuracy : 96.6% (95% CI: 92.4%~100%).

Certificate : CE ISO 13485

Key words : SARS-CoV-2 ISO13485 Rapid Neutralizing Antibody Test Kit 96.6%

OEM : OEM customized packing avaliable

Formats : 25T/box 1T/box

Sample : Blood

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SARS-CoV-2 ISO13485 Rapid Neutralizing Antibody Test Kit 96.6%

For professional and in vitro diagnostic use only.

Product Name SARS-CoV-2 ISO13485 Rapid Neutralizing Antibody Test Kit 96.6%
Formats Strip(3mm)Device(4mm) uncut sheet
Place of Origen China
Specimen Blood
Read Time 15 minutes
Shelf life 2 years
Package 25T/Box
Storage 2℃-30℃

For professional and in vitro diagnostic use only.

Advantage

  • It can not only screen in the window period of infection oneset but also indicate the previous infection and reduce the rate of missed diagnosis
  • Blood sample detection , simple samplig, simple operation
  • Combined with nucleic acid kit to improve the screening rate of suspected patients
  • Rapid screening within 10-15minutes, resukts effective for 15minutes
  • Single detection, visual interpretation, no equipment, to adapt to the community
  • Easy operation, compatible with different samples
  • Room temperature storage

[PERFORMANCE CHARACTERISTICS]

Sensitivity

The sensitivity to S-mIgG1 neutralizing antibody can reach 2ug/mL.

Accuracy

A side-by-side comparison was conducted by the results of SARS-Cov-2 Neutralizing Antibody Test Device (Test Reagent) developed by Hangzhou Deangel Biological Engineering Co., Ltd. and cPassTM from Genscript CO., Ltd. 328 clinical specimens from Professional Point of Care site were evaluated, 105 were positive and others negative. Base on the results from the clinical studies, the statistical analysis was made as follows:

cPassTM Total
Positive Negative

Test

reagent

Positive 96 2 98
Negative 9 221 230
Total 105 223 328

For test reagent, the clinical sensitivity with the “Compared Reagent” was 91.4% (95% CI: 77.7%~100%), the clinical specificity was 99.1% (95% CI: 97.2%~100%), the coincidence rate was 96.6% (95% CI: 92.4%~100%).

[SUMMARY]

The novel coronaviruses belong to the β genus. COVID-19 is an acute respiratory infectious disease. People are generally susceptible. Currently, the patients infected by the novel coronavirus are the main source of infection; asymptomatic infected people can also be an infectious source. Based on the current epidemiological investigation, the incubation period is 1 to 14 days, mostly 3 to 7 days. The main manifestations include fever, fatigue and dry cough. Nasal congestion, runny nose, sore throat, myalgia and diarrhea are found in a few cases.

OEM 25 Packs Neutralizing Antibody Rapid Test 96.6% Accuracy

OEM 25 Packs Neutralizing Antibody Rapid Test 96.6% Accuracy


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25 Packs Neutralizing Antibody Rapid Test

      

OEM 25 Packs Antibody Rapid Test

      

Neutralizing Antibody Rapid Test 96.6%

      
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