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Corona test - Import export

Germany

The TÜV-certified CLUNGSE COVID-19 antigen test is a rapid test for the qualitative detection of nucleocapsid protein antigens in nasal or nasopharyngeal swabs. The SARS-CoV-2 test listed by the BfArM may be carried out either by medical professionals or by appropriately trained professionals. The 3in1 antigen test is characterized by new batches that recognize Omikron with high specificity and are optimized for professional use. The tests are prefilled, the buffer solution bottle is sealed for error-free handling and the sample can be taken via the following swabs: nasal, oropharyngeal and nasopharyngeal. Thanks to the high sensitivity and specificity, the test result is particularly reliable. The test can already be read after 10 - 15 minutes. • 3in1 antigen test according to the Federal Institute for Drugs and Medical Devices approval AT079/20 • Format - Immunoassay​ • Sampling Nasopharyngeal swab and/or nasal • Packaging 25 tests per case

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Switzerland

Testing against enveloped viruses as a replacement for the currently unavailable commercial test strategy against 2019-nCov / SARS-CoV-2 Since the new SARS-CoV-2 virus is one of the enveloped viruses, INVITRO-CONNECT GmbH offers testing of various surfaces and disinfectants against the Vaccinia Ankara Virus (MVA) as a reference virus for enveloped viruses, as well as against the bovine coronavirus , which, like SARS-CoV-2, belongs to the genus Betacoronavirus. In addition to standard tests for surfaces in accordance with ISO 21702 (smooth surfaces) and ISO 18184 (rough surfaces) as well as suspension tests for the disinfectant area (EN ISO 14476/16777), other tests are also offered on request (see below). Named tests are currently the state-of-the-art test methods for testing against 2019-nCov / SARS-CoV-2, as there is currently no specific test procedure against the 2019-nCov / SARS-CoV-2 virus itself. For more information --> contact@invitro-connect.com

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Germany

Easy handling thanks to minimally invasive sampling as a nasal swab (2.5 cm depth) Also very good for use with small children, students, handicapped people, professional sports activities and in companies This test is Made in Germany and approved for use by laypersons Reliable with 100% sensitivity and 98% specificity

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Germany

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

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Germany

Rapid antigen test COVID-19 swab test LIFECOSM - 25 pieces - SARS-CoV-2 to the extended 4in1 successor article most sensitive rapid corona test in Germany according to the Paul Ehrlich Institute (PEI) listed at the BfArM 100% overall sensitivity according to PEI -> AT1054/21 | AT 1055/21 | AT1056/21 | AT1340/21 | AT1361/21 -> same test cassette detects current virus mutations, reliable at Omikron reimbursable by test regulation

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United Kingdom

Boson Biotech-Rapid SARS-CoV-2 Antigen test card Corona virus SELF anterior nasal swab Covid rapid antigen test. The Rapid SARS-CoV-2 Antigen test card from Boson Biotech is a covid self-diagnostic test. Registered at the Ministry of Health Min. Sal. n° 2089498 CE Mark 0123, Certificate No.: V90613170006 Rev.00 of 01/04/2021 Diagnostic sensitivity: 96.77% - Diagnostic specificity: 99.20%. DE + AT approved "Laientest" BfArM approved "Laientest" in Germany (special approval 5640-S-007/21) Austria: For home and self-applying according to §323c ABS 18 BAO approved BAG-listed High Accuracy: nasopharyngeal swab collection with clinically proven high accuracy results. Usability: any adult can easily use our three-step, cost-effective portable testing kit. Easy to Use: Testing can be easily administered in almost any environment without additional special equipment. Easy to transport with no special storage requirements, a test kit is all you need.

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Germany

With the self/rapid test you get a high-quality corona antigen self-test, which is used for the qualitative detection of SARS-CoV-2 nucleocapsid antigens in the front nasal cavity in a short time. It is based on the lateral flow immunoassay method, which uses antibodies to detect specific antigens in the sample swab.

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