Medical diagnostic tests - Import export

The Lyme IgG/IgM Rapid Test Cassette is a qualitative test kit. Detects IgG and IgM antibodies to Borrelia in whole blood, serum or plasma specimens. This test consists of two components, an IgG component and an IgM component. GP Medical Professional Testing Kits CE Marked for Professional Use

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 système tout-en-un sans bandelettes dispose de 50 tests sur un ruban continu et d'un autopiqueur intégré contenant une cartouche de 6 lancettes. Avec ce système unique il ne faut plus s’inquiéter de manquer de bandelettes ou de lancettes. Des mesures faciles et rapides en seulement 4 étapes simples.

The FlowFlex Rapid Lateral Flow Antigen Test Kit uses the latest patented technology to detect proteins, ensuring that it can detect new strains of the COVID-19 virus. Using a simple nasal swab within 2cm of the nose makes it extremely easy to administer an accurate test.

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 ▪ 25 x Test devices packaged individually in aluminium pouch ▪ 25 x Disposable test tubes with extraction buffer ▪ 25 x Filter caps ▪ 25 x Sterilised swabs for specimen collection ▪ 1 x Instructions for use *£2 ex vat per test *All prices are ex vat and shipping costs Certificates: FDA European Commission CE Marked Porton Down DHSC Manufacturer Humasis Co., LTD, South Korea EN ISO 13485:2016 Detection COVID-19 Antigen Method Immunochromatographic Assay Test Type Cassette Package 25T/Kit Specimen Nasopharyngeal or Nasal Swab Shelf Life 18 Months Storage 2-30 Celsius Test Time 15 minutes Cat No. ACOVA-7025

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

Antigen Diagnostic Kit Rapid test kit results in 20 minutes Used at the point of care by medical professionals

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

Medical device testing is tightly regulated due to the potential severity of an EMC or Safety failure. The term 'medical device' covers a wide range of items and we have extensive experience in testing in this area, covering items such as prosthetic limbs, hospital beds, patient monitors, TENS machines, blood pressure monitors, to name just a few. We are UKAS accredited to test for the Medical standards IEC/EN 60601-1 and IEC/EN 60601-1-2, covering the basic safety and essential performance of medical electrical equipment. We are also UKAS accredited for the following specific medical standards: -IEC 60601-1-11 Particular requirements for medical electrical equipment and medical electrical systems in the home healthcare environment -IEC 60601-2-10 Particular requirements for the safety of nerve and muscle stimulators Using a UKAS accredited laboratory gives manufacturers assurance accuracy, reliability and consistency.

The testing machines of model series 215 were developed and built for applications with extremely small measuring ranges, below 0.1 Ncm, and highest precision. They are for example used in watch idustry or medical technology. All torsion testing machines are equipped with the TesTController 850 that is TEDS compatible. The corresponding software TesTWinner® provides the user - besides to its free programmability - an immense repertoire of possibilities for standard test procedures and routine test execution, evaluation, presentation and further processing of results, automation of processes and much more. A wide application field is guaranteed by a comprehensive range of accessory.