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China factory - Hangzhou Aichek Medical Technology Co.,Ltd

Hangzhou Aichek Medical Technology Co.,Ltd

  • China,Hangzhou ,Zhejiang
  • Active Member

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China IVD In Vitro Diagnostic Test Kits Nasal Swab Rapid Antigen Self Test
China IVD In Vitro Diagnostic Test Kits Nasal Swab Rapid Antigen Self Test

  1. China IVD In Vitro Diagnostic Test Kits Nasal Swab Rapid Antigen Self Test

IVD In Vitro Diagnostic Test Kits Nasal Swab Rapid Antigen Self Test

  1. MOQ: 5000 Test
  2. Price: Negotiable
  3. Get Latest Price
Payment Terms T/T
Supply Ability negotiable
Packaging Details 40box/carton
Storage 2℃-30℃
User Professional
Accuracy 99.05% (95% CI: 97.58%~99.63%)
Certificate CE ISO 13485
Key words Nasal Swab Covid-19 Plastic Antigen Self Test Kit OEM ODM
OEM OEM customized packing avaliable
Formats 25T/box 1T/box
Sample Swab
Brand Name Aichek
Model Number COVID-19-G02001A
Certification CE
Place of Origin China

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  1. Product Details
  2. Company Details

Product Specification

Payment Terms T/T Supply Ability negotiable
Packaging Details 40box/carton Storage 2℃-30℃
User Professional Accuracy 99.05% (95% CI: 97.58%~99.63%)
Certificate CE ISO 13485 Key words Nasal Swab Covid-19 Plastic Antigen Self Test Kit OEM ODM
OEM OEM customized packing avaliable Formats 25T/box 1T/box
Sample Swab Brand Name Aichek
Model Number COVID-19-G02001A Certification CE
Place of Origin China
High Light IVD In Vitro Diagnostic Test KitsIVD Rapid Antigen Self TestNasal Swab Rapid Antigen Self Test

SARS-CoV-2 IVD Reagent Rapid Antigen Self Test Kit Individual Test

Product Name

SARS-CoV-2 IVD Reagent Rapid Antigen Self Test Kit Individual Test

Formats Device(4mm)
Place of Origen China
Specimen Swab
Read Time 15 minutes
Shelf life 2 years
Package 25 device/box or 1Test/Box
Storage 2℃-30℃

 

The COVID-19 Antigen Rapid Test device is a lateral flow chromatographic immunoassay for the qualitative detection of the nucleocapsid(N) protein antigen from SARS-CoV-2 in nasopharyngeal swab, oropharyngeal swab. It provides an aid in the diagnosis of infection with 2019-nCOV.

 
Limited of Detection (Analytical Sensitivity)
The detection limit of the product to SARS-CoV-2 is 50TCID50/mL. Analytical Specificity: Cross-reactivity and Interference
1. Cross-reactivity of the device was evaluated by testing, related pathogens and microorganisms that are likely to be present in the
respiratory tract. No cross-reactivity was observed with the following organisms presented in the table below.
Microorganisms Concentration of Cross-reactivity substance
Human coronavirus HKU1 1× 106TCID50 /mL
Human coronavirus OC43 1× 106TCID50 /mL
Human coronavirus NL63 1× 106TCID50 /mL
Human coronavirus 229E 1× 106TCID50 /mL
MERS-coronavirus 1× 106TCID50 /mL
Influenza A virus 1× 106TCID50 /mL
Influenza B virus 1× 106TCID50 /mL
Rhinovirus 1× 106TCID50 /mL
Adenovirus 1× 106TCID50 /mL
Enterovirus 1× 106TCID50 /mL
Human Metapneumovirus 1× 106TCID50 /mL
Parainfluenza 1× 106TCID50 /mL
Respiratory syncytial virus 1× 106TCID50 /mL
Mycoplasma pneumonia 1× 107 CFU/mL
Chlamydia pneumonia 1× 107 CFU/mL
Streptococcus pneumonia 1× 107 CFU/mL
Staphylococcus aureus 1× 107 CFU/mL
Mycobacterium tuberculosis 1× 107 CFU/mL
Haemophilus influenzae 1× 107 CFU/mL
Streptococcus pyogenes 1× 107 CFU/mL
 
 

[WARNINGS AND PRECAUTIONS]
l For in vitro diagnostic use only.
l For healthcare professionals and professionals at point of care sites.
l Do not use after the expiration date.
l Please read all the information in this manual before performing the test.
l The test device should remain in the sealed pouch until use.
l All specimens should be considered potentially hazardous and handled in the same manner as an infectious agent. Wear gloves

ifneed, don’t touch the membrane.
l The used test device should be discarded according to federal, state and local regulations.
l The test is intended to be read at 15 minutes. If the test is read before 15 minutes or after 20 minutes, false negative or false positive

results may occur, and the test should be repeated with a new test cassette.
l The test device is a disposable product. Please dispose properly after use.

 

Company Details

Bronze Gleitlager

,

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 and 

Graphite Plugged Bushings

 from Quality China Factory
  • Business Type:

    Manufacturer

  • Year Established:

    2012

  • Total Annual:

    500000-1000000

  • Employee Number:

    150~200

  • Ecer Certification:

    Active Member

Hangzhou Aichek Medical Technology Co.,Ltd Hangzhou Aichek Medical Technology Co.,Ltd is a high-tech company specialises in manufacturing rapid diagnostic and healthcare products.   With five product lines of fertility, infectious diseases, cardiac marker, tumor marker and drug of... Hangzhou Aichek Medical Technology Co.,Ltd Hangzhou Aichek Medical Technology Co.,Ltd is a high-tech company specialises in manufacturing rapid diagnostic and healthcare products.   With five product lines of fertility, infectious diseases, cardiac marker, tumor marker and drug of...

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Get in touch with us

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  • Hangzhou Aichek Medical Technology Co.,Ltd
  • 3rd Floor, Building 9, Hexiang Technology Center, Xiasha Street, Qiantang District, 310018 Hangzhou, Zhejiang, P.R. China
  • https://www.rapidstests.com/

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