Payment Terms | T/T |
Supply Ability | negotiable |
Packaging Details | 40box/carton |
Storage | 2℃-30℃ |
Sample Type | Blood |
User | Professionals |
Accuracy | 94.67% (95% CI: 91.57%~97.77%). |
Certificate | CE ISO 13485 |
Key words | Professional and Convenient COVID-19 antibody rapid test device |
OEM | OEM customized packing avaliable |
Formats | 25T/box 1T/box |
Brand Name | Aichek |
Model Number | COVID-19-G02001A |
Certification | CE |
Place of Origin | China |
View Detail Information
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Product Specification
Payment Terms | T/T | Supply Ability | negotiable |
Packaging Details | 40box/carton | Storage | 2℃-30℃ |
Sample Type | Blood | User | Professionals |
Accuracy | 94.67% (95% CI: 91.57%~97.77%). | Certificate | CE ISO 13485 |
Key words | Professional and Convenient COVID-19 antibody rapid test device | OEM | OEM customized packing avaliable |
Formats | 25T/box 1T/box | Brand Name | Aichek |
Model Number | COVID-19-G02001A | Certification | CE |
Place of Origin | China | ||
High Light | COVID-19 Antibody Test Device ,4mm Antibody Test Device ,4mm Antibody Rapid Test Kit |
Professional and Convenient COVID-19 antibody rapid test device
For professional and in vitro diagnostic use only.
Product Name | OEM SARS-COV-19 IgG IgM Antibody Rapid Test Kit |
Formats | Strip(3mm)Device(4mm) uncut sheet |
Place of Origen | China |
Specimen | Blood |
Read Time | 15 minutes |
Shelf life | 2 years |
Package | 25 device/box |
Storage | 2℃-30℃ |
[INTENDED USE]
The COVID-19 IgG/IgM Rapid Test device is a lateral flow chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Novel coronavirus in human Whole Blood/Serum/Plasma. It provides an aid in the diagnosis of infection with Novel coronavirus.
[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.
[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.
• Please read all the information in this leaflet before performing the test.
• The test device should remain in the sealed pouch until use.
• All specimens should be considered potentially hazardous and handled in the same
manner as an infectious agent.
• Because there is a window period for the time when the body produces antibodies
after infection and the types and amounts of antibodies produced by different human
bodies at different time periods are various, it will cause individual differences in
actual test results.
• The used test device should be discarded according to federal, state and local
regulations.
Company Details
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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