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Sugentech SGTi-flex COVID-19 Ag is an immunoassay for qualitative detection of Nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal and nasal swab specimen. • Specimen: Nasopharyngeal (or Nasal) swab • One Step, Fast results within 15 min • Full package for the whole test procedure, No need for additional tool/device - Swab - Buffer - Test Cassette • Package: 5 test kits *all prices are ex vat * shipping is free on orders over 1000 units to one location Product No. CAGT001E0 Description COVID-19 Antigen Lateral Flow Test. For self-testing only. Approvals CE Marked, MHRA registered Intended Use An immunoassay for qualitative detection of Nucleocapsid protein antigen from SARS-CoV-2 in nasal swab specimen. Accuracy Overall Accuracy Sensitivity Specificity 97.35% 95.07% 99.38% Package Each test is individually boxed Specimen Nasal Swab Storage 2-30 Celsius Test Time 15-30 minutes CE Marked US FDA MHRA Compliant European Commission

The Humasis COVID-19 Test is an in vitro diagnostic test based on lateral flow chromatographic immunoassay intended for qualitative detection of SARS-CoV-2 antigen in human nasopharynx. For healthcare professional use in near patient testing environments. Sensitivity 95.5% & Specificity 100% Kit Contents ▪ 1 x Test devices packaged individually in aluminium pouch ▪ 1 x Disposable test tubes with extraction buffer ▪ 1 x Filter caps ▪ 1 x Sterilised swabs for specimen collection ▪ 1 x Instructions for use *All prices are ex vat *£2 ex vat per test * shipping is free for orders over 1000 units

Sugentech SGTi-flex COVID-19 Ag is an immunoassay for qualitative detection of Nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal and nasal swab specimen. • Specimen: Nasopharyngeal (or Nasal) swab • One Step, Fast results within 15 min • Full package for the whole test procedure, No need for additional tool/device - Swab - Buffer - Test Cassette • Package: 1 test kit *all prices are ex vat * shipping is free on orders over 1000 units to one location Product No. CAGT001E0 Description COVID-19 Antigen Lateral Flow Test. For self-testing only. Approvals CE Marked, MHRA registered Intended Use An immunoassay for qualitative detection of Nucleocapsid protein antigen from SARS-CoV-2 in nasal swab specimen. Accuracy Overall Accuracy Sensitivity Specificity 97.35% 95.07% 99.38% Package Each test is individually boxed Specimen Nasal Swab Storage 2-30 Celsius Test Time 15-30 minutes CE Marked US FDA MHRA Compliant European Commission

Sugentech SGTi-flex COVID-19 Ag is an immunoassay for qualitative detection of Nucleocapsid protein antigen from SARS-CoV-2 in nasopharyngeal and nasal swab specimen. • Specimen: Nasopharyngeal (or Nasal) swab • One Step, Fast results within 15 min • Full package for the whole test procedure, No need for additional tool/device - Swab - Buffer - Test Cassette • Package: 2 test kits *all prices are ex vat * shipping is free on orders over 1000 units to one location Product No. CAGT001E0 Description COVID-19 Antigen Lateral Flow Test. For self-testing only. Approvals CE Marked, MHRA registered Intended Use An immunoassay for qualitative detection of Nucleocapsid protein antigen from SARS-CoV-2 in nasal swab specimen. Accuracy Overall Accuracy Sensitivity Specificity 97.35% 95.07% 99.38% Package Each test is individually boxed Specimen Nasal Swab Storage 2-30 Celsius Test Time 15-30 minutes CE Marked US FDA MHRA Compliant European Commission

Diagnostic Automation offers a One-Step Malaria Rapid diagnostic Test for Malaria pf and pv antigens. This Malaria Rapid Test is a rapid, qualitative test for the detection of Plasmodium falciparum and/or Plasmodium vivax in whole blood. For the rapid qualitative determination of Malaria P. falciparum pecific histidine rich protein-2 (Pf HRP-2) and Malaria P. vivax specific lactate dehydrogenase (pvLDH) in human blood as an aid in the diagnosis of Malaria infection. Diagnostic Automation offers two formats of the Malaria Rapid Test.

Ce simple test salivaire permet de détecter la consommation de 6 drogues différentes en même temps. Il s'agit des drogues suivantes : - Cocaïne - Amphétamine - Cannabis (herbe, haschich) - Opiacés (héroïne, morphine, codéine) - Méthamphétamines - Fenciclidine. Le test salivaire multi-drogues se base sur le principe des réactions immunochimiques rapides entre les antigènes et les anticorps, qui sont utilisés lors de la recherche de substances spécifiques dans la salive. En règle générale, les traces de drogues dans la salive après la dernière utilisation peuvent être détectées dans les délais suivants : Amphétamines, Méthamphétamines : de 5-10 minutes à 72 heures. Cocaïne : de 5-10 minutes à 24 heures. Opiacés : codéine utilisée par voie orale 7-21 heures, morphine (métabolites de la codéine et de l'héroïne 24-48 heures). Cannabis : jusqu'à 14 heures après la dernière consommation. Fenciclidine : dépend de la quantité utilisée.

COVID-19 Test kit Bioteke has developed the COVID-19 antigen test cassette 3in1 for quick detection. The COVID-19 Antigen Rapid Test Cassette is a rapid chromatographic immunoassay for the qualitative detection of Covid-19 antigen in the nasopharynx, oropharynx and nasal swabs, to support the diagnosis of a Covid-19 virus infection. Rapid tests are individually packaged and are therefore ideally intended for quick use. The special features are the easy sampling, easy to read and clearly displayed results and the result is available even after 15-20 minutes. Technical specifications Bioteke Pack • 20 pack Carton • 25 boxes – 500 pieces Standards – and market conformity • Professional application (only for professional use) • Rapid test 3 in 1 • TÜV Süd EN ISO 13485:2016 • BFarm number: AT082 / 20 • CE certified and reimbursable test listed at the Federal Institute for Drugs and Medical Devices according to the Coronavirus Test Ordinance TestV • 97.6% sensitivity • 98.

The Sentebiolab Senteligo™️ SARS-CoV-2 (COVID-19) Multiplex qPCR Detection test includes a Primer-Probe set inside the Reaction Mix that contains primers and probes for human RNaseP and viral N1 and N2 regions. The internal control (primer/probe set for human RNaseP gene) is used to identify possible qPCR inhibition, confirm the integrity of the reagents, and verify the quality of RNA extraction from patient material. RNaseP primers and probes included in the kit recognize the human RNaseP gene. The primers and probes for viral N1 and N2 regions specifically identify two distinct regions on the nucleocapsid (N) gene of the SARS-CoV-2 virus. These primers and probes do not recognize the SARS-CoV virus, whose genetic structure is highly similar to SARS-CoV-2.

COVID-19 Test kit Greentspring has developed the COVID-19 antigen test cassette 4 in1 for quick detection. The COVID-19 Antigen Rapid Test Cassette is a rapid chromatographic immunoassay for the qualitative detection of Covid-19 antigen in the lolli, nasopharynx, oropharynx and nasal swabs, to support the diagnosis of a Covid-19 virus infection. Technical specifications Greenspring • 1 Box / 25 pack • Professional application (only for professional use) • Rapid test 4 in 1 • Approved in Germany • EN ISO 13485:2016 • BFarm number: AT417/20 • CE certified and reimbursable test listed at the Federal Institute for Drugs and Medical Devices according to the Coronavirus Test Ordinance (TestV) • 96.77% sensitivity • 100% specificity • With a integrated buffer solution

COVID-19 Test kit Testsealabs has developed the COVID-19 antigen test cassette 3in1 for quick detection. The COVID-19 Antigen Rapid Test Cassette is a rapid chromatographic immunoassay for the qualitative detection of Covid-19 antigen in the nasopharynx, oropharynx and nasal swabs, to support the diagnosis of a Covid-19 virus infection. Technical specifications Testsealabs • 1 Box / 25 pack • Professional application (only for professional use) • Rapid test 3 in 1 • Approved in Germany • TÜV Süd EN ISO 13485:2016 • BFarm number: AT082 / 20 • CE certified and reimbursable test listed at the Federal Institute for Drugs and Medical Devices according to the Coronavirus Test Ordinance (TestV) • 97.6% sensitivity • 98.4% specificity • With a separate buffer solution

Easy to use with results in 15 minutes Reliable with a specificity of 99.2% and a sensitivity of 96.1% BfArM listed and evaluated by the PEI (Paul Ehrlich Institute). CE-certified as a self-test for self-use