Test kit for self testing - Import export

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.

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.

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