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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.

Antigen-COVID-19 Virus Test Kit (Colloidal gold) 25pcs/kit High quality Fast delivery CE certified

Elisa test kits Name specification method Hav-igm 48 elisa serum without dilution Hav-igm 48 elisaserum with dilution Hav-igg 48 elisaserum with dilution Ana 48 elisa Anti-hbs Hbsag 2x48 elisa Anti-hbe 2x48 elisa Hbeag 2x48 elisa Anti-hbc 2x48 elisa Anti-hcv igm 48 elisa Anti-hcv igg 2x48 elisa Anti-hdv igm 48 elisa Anti-hdv igg 48 elisa Anti-hev igm 48 elisa Anti-hev igg 48 elisa Anti-hgv igm 48 elisa Anti-hgv igg 48 elisa Anti-hiv1/2 96 elisa Anti-uu 48 elisa Anti-mh 48 elisa Anti-mg 48 elisa Anti-ct 48 elisa Anti-ng 48 elisa Cmv-igm 48 elisa Toxo-igg 48 elisa Toxo-igm 48 elisa Rv-igg 48 elisa Rv-igm 48 elisa Hsv(no.1)igm 48 elisa Hsv(no.2)igm 48 elisa Anti-sperm igm 48 elisa Anti-sperm igg 48 elisa Anti-mg igm 48 elisa Anti-mg igg 48 elisa Anti-acl 48 elisa Hcg-igm 48 elisa Hcg-igg 48 elisa Anti-mp 48 elisa Anti-cpn 48 elisa Anti-hp 48 elisa Anti-tpg 48 elisa Anti-hcmv 2x48 elisa Anti-psa 2x48 elisa Anti-cea 2x48 elisa Anti-hpv 48 elisa Anti-av 48 elisa Anti-tb 48 elisa Anti-cvb 48 elisa Serum fe 48 elisa Anti dna 4 centigrade test box Hbv kit 20 pcr Hpr kit 20 pcr Ng kit 20 pcr Hsv kit 20 pcr Ct kit 20 pcr Uu kit 20 pcr Ebv kit 20 pcr Mp kit 20 pcr B19 kit 20 pcr Vc kit 20 pcr Sh kit 20 pcr St kit 20 pcr Lp kit 20 pcr Sau kit 20 pcr Tpg kit 20 pcr Mg kit 20 pcr Mh kit 20 pcr Hp kit 20 pcr Anti-dna-tm-hyb kit Ct-hyb kit 16 pcr Hbv hyb kit 16 pcr Tb hyb kit 16 pcr Hcv hyb kit 16 pcr Ng hyb kit 16 pcr Uu hyb kit 16 pcr Hpv hyb kit 16 pcr Hsv hyb kit 16 pcr Mp hyb kit 16 pcr Hgv hyb kit 16 pcr Cvb hyb kit 16 pcr Telomerase trap hyb kit 16 pcr Hot-start taq dna poly 20 pcr Rt 20 pcr Rt-rna enzyme mix kit 20 pcr Rna test kit Hcv kit 10 pcr Hrv kit 10 pcr Hiv kit 10 pcr Rv kit 10 pcr Jbev kit 10 pcr Cvb kit 10 pcr Hgv kit 10 pcr Uu media kit 6 Mh media kit 6 Mg media kit 6

Dengue rapid test kit.

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

Products - Human Chorionic Gonadotropin (HCG) Test Midstream (Colloidal Gold Immunochromatographic Assay) Product Description - Sensitivity: 25 mIU/ml Accuracy: > 99.5% ISO13485 & CE approved INTENDED USE Easy-Sweet hCG Test Midstream is an in vitro diagnostic (IVD) qualitative test for rapid detection of hCG in urine. This test is designed for self-testing use only. PRINCIPLE Easy-Sweet. hCG Midstream is two-side sandwich immunoassay for the qualitative determination of human chorionic gonadotropin (hCG) in urine. The membrane was precoated with anti alpha hCG capture antibodies on the test band region and goat anti mouse on the control band region. During the test, the urine specimen is allowed to react with anti beta hCG monoclonal antibody-colloid gold conjugate, which was predried on the test Midstream. The mixture then moves forward on the membrane by the capillary action. For a positive specimen, the conjugate binds to the hCG forming an antibody-antigen complex. This complex is captured by anti alpha hCG antibody on the test region to produces a visual pink color band when hCG concentration in specimen is equal to or greater than 25 mIU/ml. Regardless of the presence of hCG, as the mixture continues to move across the membrane to the control band region, the complex is captured by immobilized goat anti mouse antibodies to form a distinct pink colored control band. The presence of the control band indicated: 1) a normal flow is obtained, 2) antibody pre-coated on control line and colloidal gold conjugate are functional. 1 pc/individual pouch , 500pcs/ctn or customized

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.

The CorDx HCG PREGNANCY TEST MIDSTREAM KIT FOR SELF TESTING is a rapid test for the qualitative detection of human chorionic gonadotropin (hCG) in urine species to aid in the early detection of pregnancy. It is intended for home users and for prescription use. Featuresï¼? accuracy>99.5% sensitivity: 25miu /ml rapid: result is readable as quick as in 1 minute. specimen: urine, widely used for self-testing. shelf life: 36months or 24months packing:1pc/box, 3pcs/box CE and FDA approved

Coronavirus/covid-19 quick test kit / covid-19 diagnostic kit price as low as 2.1 USD/test quick PCR test only 2.3 USD/test moq 1 mil

Manufacturer: Shanghai LiangRun Biomedicine Technology Co.,Ltd. Certificates: CE(EU), MHRA(UK), HSA(Singapore), MDA(Malaysia), TSE(Turkey), DIGEMID(Peru), Luxus Medical(Germany) , FDA(US), EUA(US, Registering) FOB: 10m, 4.5usd

dear my friend, we are from Lepu Medical, the manufacturer for the self testing kits. we are offering the goods will CE and also very fast production time. Starting from the IVD test, our products now is hot welcomed in the world. You may freely contact with us in the WhatsApp 008613230113351 or maybe the email address at dannis.wen@lepu-medical.com we are opening for the worldwide buyers to have the goods. If you need, you can also find our in our web or Alibaba. We are willing to meet and make new friends around the world.

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.