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Thermo Scientific™ ASAPath™ COVID-19 Antigen Rapid Test (CE-IVD)
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Obtain COVID-19 test results fast with the easy-to-use, disposable Thermo Scientific ASAPath COVID-19 Antigen Rapid Test.
Obtain COVID-19 test results within 30 minutes with the fast, easy-to-use, disposable Thermo Scientific™ ASAPath™ COVID-19 Antigen Rapid Test. This test is a qualitative lateral flow immunoassay intended to detect the nucleocapsid protein from the SARS-CoV-2 virus, which causes COVID-19, in nasal swab samples from symptomatic individuals who are suspected of COVID-19 by a healthcare professional, or individuals with or without symptoms or other epidemiological reasons to suspect COVID-19 infection.
- Rapid Antigen Test for COVID-19
- Detect nasal swab sample
- Kit contains 10 sets of tests
- Easy nasal swab sample collection
- Test can be done by a single person
- Results within 30 minutes
- Easy-to-read results
- No special reader necessary
- Antibody pool targeting several virus protein regions for variant detection
- Single use, disposable device
Specifikationer
Specifikationer
| Innehåll och lagring | Room Temperature |
| Beskrivning | ASAPath™ COVID-19 Antigen Rapid Test (CE-IVD) |
| Inkluderar | One kit contains ten (10) Antigen Rapid Tests, each of which includes cassette, swab, extraction tube, dropper cap, and tube stand |
| Kvantitet | 1 Kit |
Säkerhet och hantering
- X10 ASAPath Covid-19 Antigen Rapid Test
- Varning
- FARA FÖR SKADLIGA LÅNGTIDSEFFEKTER (FÖR VATTENMILJÖN) Kategori\: kronisk 1
- AKUT FARA (FÖR VATTENMILJÖN) Akut1
- H410-Mycket giftigt för vattenlevande organismer med långtidseffekter.
- P273-Undvik utsläpp till miljön.
- P391-Samla upp spill.
- P501b-Innehållet/behållaren lämnas till I enlighet med lokala / regionala / nationella / internationella bestämmelser (ska anges).
- MIXTURE LIST-Innehåller: Hexadecan-1-yl(trimethyl)ammonium chloride
Product is CE Marked but not 510(k) cleared nor authorized for Emergency Use in US and not yet available for sale in the U.S. Availability of the product in each country depends on local regulatory marketing authorization status.
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