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Hiv test kit

99% above sensitivity and specificity
Anti-hiv 1/2 or anti-hiv tri-line, which can tell hiv 1 or hiv 2 positive seperately

Single pouched, then in bulk or in box

Dengue rapid test kit.

Our LH rapid test is based on the theory of enzyme interaction. It could be used to detect the content of LH atom in urine speciment. And the colour change will identify the result directly. Assisting with the result,doctor could judge whether the patient is pregnant .


2.5mm, 200 strips/pouch, 10,000strip /case ,27kg
3.0mm, 50 kits/ pouch, 2,000 kits/case, 27kg
4.0mm, 150 cards/pouch, 2,500 cards/case, 25kg
5.0mm
10000strips/case 2000kits/case 2500cards/case.

Our product is based on the theory of enzyme interaction. It is used to detect the HCG atom in urine speciment. The colour change could identify the test result directly. Assisting with the result,doctor could judge whether the patient is pregnant or not.


2.5mm, 200 strips/pouch, 10,000strip /case ,27kg
3.0mm, 50 kits/ pouch, 2,000 kits/case, 27kg
4.0mm, 150 cards/pouch, 2,500 cards/case, 25kg
5.0mm
10000strips/case 2000kits/case 2500cards/case.

HCG Pregnancy rapid test
Home Test
CE approved
Strip , Cassette , Midstream
10miu ,25miu.


2.5mm, 200 strips/pouch, 10,000strip /case ,27kg
3.0mm, 50 kits/ pouch, 2,000 kits/case, 27kg
4.0mm, 150 cards/pouch, 2,500 cards/case, 25kg
5.0mm
10000strips/case 2000kits/case 2500cards/case.

Angiten-COVID-19 Virus Test Kit (Colloidal Gold)
Quantity of box: 25 persons/box
Brand: Easysweet
NMPA (National Medical Products Administration): Approved
CE: with CE mark
BfArM: listed
Test Method: Antigen Test
Result Time: 10-15 mins
Sample Type: Nasal Swab
Sensitivity: 96.70%
Specificity: 100%
Accuracy: 98.94%
Shelf Life: 24 months
Storage Temperature: 2-30 Degree Celsius
Country of Origin: Made in China
Additional Information:
Production Capacity: 1 million
Delivery Time: 10-15 days
Packaging Details: 25 tests in a pack, 40packs/ carton
Angiten-COVID-19 Virus Test Kit is an in vitro diagnostic rapid test for the qualitative detection of SARS-CoV-2 antigen (Ag) in human nasopharyngeal swab specimens from individuals who meet COVID-19clinical and / or epidemiological criteria. It can be used by professional only.

The CorDx COVID-19 Ag Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus.
View File Non-prescription home use for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected anterior nasal (nares) swab samples from individuals aged 2 years or older. This test is authorized for individuals with symptoms of COVID-19 within the first 7 days of symptom onset when tested at least twice over three days with at least 48 hours between tests, and for individuals without symptoms or other epidemiological reasons to suspect COVID-19, when tested at least three times over five days with at least 48 hours between tests.

The CorDx COVID-19 Ag Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus.
View File Non-prescription home use for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus with self-collected anterior nasal (nares) swab samples from individuals aged 14 years or older or adult collected anterior nasal (nares) swab samples from individuals aged 2 years or older. This test is authorized for individuals with symptoms of COVID-19 within the first 7 days of symptom onset when tested at least twice over three days with at least 48 hours between tests, and for individuals without symptoms or other epidemiological reasons to suspect COVID-19, when tested at least three times over five days with at least 48 hours between tests.

20 tests/box

covid antigen nasal rapid test passed the Germany PEI testing and registered on EU Common List

20 tests/box, 1 pcs/box, 5pcs/box

The product is based on the principle of antigen-antibody reaction and immunoassay technique. The test device contains colloidal gold labeled SARS-CoV-2 recombinant protein, mouse-anti human IgG antibody immobilized in G test area, mouse-anti human IgM antibody immobilized in M test area and the corresponding antibody in quality control area (C).
During the test, when the SARS-CoV-2 IgM antibody level in the sample is at or above the limit of detection of the test, the SARS-CoV-2 IgM antibody in the sample binds to the colloidal gold labeled SARS-CoV-2 recombinant protein which is pre-coated on a gold label pad. The conjugates migrate upward through capillary effect and would be captured by mouse-anti human IgM antibody immobilized in M test area subsequently and this produces a purple-red band appears in the M test area. When the SARS-CoV-2 IgG antibody level in the sample is at or above the limit of detection of the test, the SARS-CoV-2 IgG antibody in the sample binds to the colloidal gold labeled SARS-CoV-2 recombinant protein which is pre-coated on a gold label pad. Theconjugates migrate upward through capillary effect and would be captured by mouse-anti human IgG antibody immobilized in G test area subsequently and this produces a purple-red band appears in the G test area. If it is a negative sample, there is not a purple-red band appeared in the M and G test area. Regardless of the presence or absence of the SARS-CoV-2 antibody in the sample, a purple-red band will appear in the quality control area (C). The purple-red band in the quality control area (C) is a criterion for judging whether there is enough sample and whether the chromatography process is normal. It also serves as the internal control standard for reagents.

The CorDx COVID-19 Ag Test is a lateral flow immunoassay device intended for the qualitative detection of nucleocapsid protein antigen from the SARS-CoV-2 virus.

EUA and CE pass
shelf life: 24months since manufacturing date
packing:2pcs/box,4pcs/box and so on

It is for self testing and OTC, for home use, school , and any group .

Flu A H5 subtype Antigen Rapid Test Kit/Flu A H7 subtype Antigen Rapid Test Kit/Flu A H9 subtype Antigen Rapid Test Kit. They're highly sensitive, high specificity, and it's easy to use. Because the company is manufacturer, we can offer better quality at reduced prices.

Our fist products such as HCG, LH, and HIV test, they are selling very well and have excellent market in the world.


4.0mm, 150 cards/pouch, 2,500 cards/case, 25kg
2500cards/case.

Hcg test

Sensitivity of 25 miu or 10 miu

Single test in pouch, the in box or in bulk

The H pylori can be utilized as a rapid screening process for large populations of patients and highly indicated in the early diagnosis of H pylori infection as the immune response can often precede clinical manifestations of disease From a diagnostic point of view, a high serum level specific antibodies against H pylori must be interpreted as an indication of type B asymptomatic gastritis

Specification:
Specimen:Serum/plasma/whole blood
Sensitivity:96%
Specificity:90%
Packaging:25 cassettes/box,
Certificate:CE and ISO 13485
Raw materials is imported from US
OEM packaging is available

Till now we already exported 20 million tests and we can promise you very high quality.

25 tests/box, CE Mark and ISO, Clinical report, Certificate of analysis (COA) available

Clinical specify >98.89%
Accuracy: 93.41%
Specimen: whole blood/serum, 10 minutes to get results

Hi need covid-19 igg/igm rapid tear cassette? Promise you very high quality, and till now we already export more than 20 million tests and our Europe client said our product this way: you are the brain the world

COVID-19 Ag Rapid Test Device

A RAPID TEST FOR THE QUALITATIVE DETECTION OF NOVEL CORONAVIRUS ANTIGENS IN NASAL SWAB AND NASAL ASPIRATE SPECIMENSS.

Relative sensitivity: 84.4%
Relative specificity: >99%
Overall agreement: 97.8%
Specimen: swab, 10-20 minutes to get results