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 | Safe Reliable Economic |
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 |
View Detail Information
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Product Specification
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 | Safe Reliable Economic |
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 | SARS-COV-2 Saliva Antigen Rapid Test ,Home Rapid Antigen Test Kit Saliva ,25pcs Saliva Antigen Rapid Test |
Product Name | SARS-COV-2 nCov 19 Saliva Antigen Rapid Test kit home device |
Formats | Device(4mm) |
Place of Origen | China |
Specimen | Saliva |
Read Time | 15 minutes |
Shelf life | 2 years |
Package | 25 device/box or 1Test/Box |
Storage | 2℃-30℃ |
[INTENDED USE]
The COVID-19 Antigen Home Test (Saliva) is a lateral flow chromatographic immunoassay intended for the qualitative detection of the nucleocapsid protein antigen from SARS-CoV-2 in saliva specimen directly from individuals within 7 days of symptom onset to suspect COVID-19 infection. The COVID-19 Antigen Home Test (Saliva) is intended for self-use or lay person testing in a non-laboratory setting.
[PRINCIPLE OF THE TEST]
This test uses double-antibody sandwich to legally detect the antigen of novel coronavirus (2019-nCoV) in saliva samples. During detection, the gold labeled anti-2019-nCoV monoclonal antibody in the labeling pad binds to the 2019-nCoV antigen in the sample to form a complex, and the reaction complex moves forward along the nitrocellulose membrane under the action of chromatography, it is captured by the anti-2019-nCoV monoclonal antibody pre-coated by the detection zone (T) on the nitrocellulose membrane, and finally a red color reaction line is formed in the T zone. If the sample does not contain 2019-nCoV antigen, a red color reaction line cannot be formed in the T zone. Regardless of whether the sample to be tested contains 2019-nCoV antigen, a red reaction line will always form in the quality control area (C).
Product Feature
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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