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CE 1pc Neutralising Antibody Test Kit 3mm Strip 15min NAbs Test

Categories Neutralizing Antibody Rapid Test
Brand Name: Aichek
Model Number: COVID-19-G02001A
Certification: CE
Place of Origin: China
MOQ: 5000 Test
Price: 1.2 USD
Payment Terms: T/T
Supply Ability: negotiable
Packaging Details: 40box/carton
Storage: 2℃-30℃
User: Everyone
Accuracy: 99.05% (95% CI: 97.58%~99.63%)
Certificate: CE ISO 13485
Key words: SARS-CoV-2 neutralizing Antibody Rapid Test Kit CE certificate
OEM: OEM customized packing avaliable
Formats: 25T/box 1T/box
Sample: Blood
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CE 1pc Neutralising Antibody Test Kit 3mm Strip 15min NAbs Test

SARS-CoV-2 neutralizing Antibody Rapid Test Kit CE certificate

For professional and in vitro diagnostic use only.

Product NameSARS-CoV-2 neutralizing Antibody Rapid Test Kit CE certificate
FormatsStrip(3mm)Device(4mm) uncut sheet
Place of OrigenChina
SpecimenBlood
Read Time15 minutes
Shelf life2 years
Package25T/Box
Storage2℃-30℃

For professional and in vitro diagnostic use only.


[INTENDED USE]


The product is suitable for qualitative detection of neutralizing antibodies (NAbs) against SARS-CoV-2 that block the interaction between the receptor binding domain (RBD) of the spike glycoprotein and the Angiotensin converting enzyme Ⅱ (ACE2) receptor. The device can be instrumental in vaccine and therapeutic development as it is suitable for all antibody isotypes. It may also help in current COVID-19 investigations of sero-prevalence, assessment of human immunity, longevity of protective immunity, efficacy of different vaccine candidates as well as tracking infection.


[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:

cPassTMTotal
PositiveNegative

Test

reagent

Positive96298
Negative9221230
Total105223328

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%).


[WARNINGS AND PRECAUTIONS]

  • For in vitro diagnostic use only.
  • For healthcare professionals and professionals at point of care sites.
  • Do not use after the expiration date.
  • Do not mix reagents from different batches.
  • Please read all the information in this leaflet before performing the test.
  • The test device should remain in the hermetic bag until use.
  • All specimens should be considered potentially hazardous and handled in the same manner as an infectious agent.
  • The used test device should be discarded according to federal, state and local regulations.


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