Accu check active test strip and performa strips.
Ovulation and pregnancy tests kits.
Medical devices : human and veterinary diagnostic rapid diagnostic kits.
Antigen rapid test kits.
Rapid antigen test kits..
Antigen Rapid Test Kits.
Diagnostic reagent tests kits.
Rapid antigen test kit.
Real time pcr kits, rna extraction kits, rapid antigen test, vtm kit and ngs kits for covid 19.complete covid19 testing solutions, rapi q poc rapid rt pcr solutions.
Test Antigen.
Medical test kits like hirikon hiv 1/2 saliva home test kits.
Rapid test kit, hiv, hbsag, hcv, malaria, dengue, typhoid.
Rapid Diagnostics Test Kit.
Core diagnostic & rapid test kits and molecular kits..Manufacturer
Elisa Kits.
Diagnostic Kits Rapid Test Kits .
Rapid Test Kits Diagnostic Kits .
Diagnostic Kits Rapid Test Kits .
Antigen antibody rapid test kits.
Anti-SARS-CoV-2 Rapid Test, COVID-19 1. Easier: No special equipment needed, Intuitive visual interpretation. 2. Rapid: Quick sampling by fingertip blood, Results in 10-15min. 3. Accurate: Results with IgG and IgM respectively. 4. Application: as screening tool for potential suspect patients in large numbers. Testing kit is FDA Emergency Use Authorization (EUA) Approved Testing kit is CE MARKED-IVD * Instruction for Use * Interpretation Guide * SARS-CoV-2 immunoassays * Accuracy of the Anti-SARS-CoV-2 Rapid Test Kit * Anti-SARS Rapid Test Brochure * COVID-19 Catalog * EUA Approval Letter * Fact Sheet for Healthcare Providers * FDA Letter * Fact Sheet for Recipients * FAQ * CE IVD Notification Certificate Antibody Performance Measure Estimate of Performance 95% Confidence Interval IgM Sensitivity (PPA) 95.7% (289/302) (92.8%; 97.5%) IgM Specificity (NPA) 99.7% (311/312) (98.2%; 99.9%) IgG Sensitivity (PPA) 99.0% (299/302) (97.1%; 99.7%) IgG Specificity (NPA) 99.4% (310/312) (97.7%; 99.8%) Combined Sensitivity (PPA) 99.0% (299/302) (97.1%; 99.7%) Combined Specificity (NPA) 99% (309/312) (97.2%; 99.7%) Combined PPV at prevalence = 5% 84.4% (64.6%; 94.6%) Combined NPV at prevalence = 5% 99.9% (99.8%; 100%) Testing kit is FDA Emergency Use Authorization (EUA) Approved Testing kit is CE MARKED-IVD * Instruction for Use * Interpretation Guide * SARS-CoV-2 immunoassays * Accuracy of the Anti-SARS-CoV-2 Rapid Test Kit * Anti-SARS Rapid Test Brochure * COVID-19 Catalog * EUA Approval Letter * Fact Sheet for Healthcare Providers * FDA Letter * Fact Sheet for Recipients * FAQ * CE IVD Notification Certificate
