Abbott Panbio COVID-19 -antigeenin nopea testi

Näyte: Matala nenä
Muoto: Kasetti
Aika tulokseen: 15 minuuttia
Määrä: 25 testiä / laatikko
Volyymihinnoittelu:

16 dollaria / testi – 25-75 testiä (1-3 laatikkoa)
15 dollaria / testi – 100-475 testiä (4-19 laatikkoa)
14,00 $ / testi – 500-999 testiä (20-39 laatikkoa)
Yli 1000 testiä – ota meihin yhteyttä saadaksesi tarjouksen

Panbio COVID-19 Ag -pikatestilaite (nenän kautta) on korkean suorituskyvyn pikatesti potilaille, joita epäillään nykyisestä COVID-19-infektiosta.

Panbio mahdollistaa välittömän käsittelyn tai eristystoimenpiteet tartunnan minimoimiseksi.

  • Potilasystävälliset nenän tai nenänielun näytteenottotyypit.
  • Helppokäyttöinen ja laajamittainen testaus auttaa torjumaan viruksen leviämistä.
  • Mahdollisesti tarttuvien henkilöiden nopea tunnistaminen
  • Testitulokset 15 minuutissa
  • Ota käyttöön laajamittaisesti hoitopaikassa
  • Voidaan käyttää monissa muissa kuin laboratorioissa
  • Erityisiä / lisälaitteita ei tarvita
  • Itsenäinen putki, jossa on irrotettava vanupuikko, vähentää henkilöstön altistumista
  • Uuttoputki on täysin suljettu hävitettäväksi

SARS-CoV-2 Rapid Antigen Test Nasal

9901-NCOV-03G 25 Tests/Kit
EUR 112.8
Description: The SARS-CoV-2 Rapid Antigen Test is a lateral fl ow rapid chromatographic immunoassay for the qualitative detection of nucleocapsid antigen to SARS-CoV-2 present in human nasal samples. This test is intended for use as an aid in detection of SARS-CoV-2 infection in individuals suspected of COVID-19 with clinical symptoms onset within 5 days. Results are for the identification of SARS-CoV-2 nucleocapsid antigen. Antigen is generally detectable in human nasal swab samples during the acute phase of infection. Positive results indicate the presence of viral antigens, but clinical correlation with patient history and other diagnostic information is necessary to determine infection status. Positive results do not rule out bacterial infection or co- infection with other viruses. The agent detected may not be the definite cause of disease. Negative results should be treated as presumptive, and do not rule out SARS-CoV-2 infection and should not be used as the sole basis for treatment or patient management decisions, including infection control decisions. Negative results should be considered in the context of a patient’s recent exposures, history and the presence of clinical signs and symptoms consistent with COVID-19, and confirmed with a molecular assay, if necessary, for patient management. The SARS-CoV-2 Rapid Antigen Test is intended for use in laboratory or POC settings by healthcare professionals, or self-collection under the supervision of a healthcare worke

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Coronavirus (SARS-Cov-2) Antigen Rapid Test Device (Saliva)

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TruStrip RDT Anthrax Protective antigen 83 (PA83) Rapid Test cards, 25/pk

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Brucella Antibody Rapid Test Kit

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Quinolones (QNs) Rapid Test Kit

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Salbutamol (SAL) Rapid Test Kit

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Quinolones (QNs) Rapid Test Kit

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Clenbuterol (CLE) Rapid Test Kit

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Ractopamine (RAC) Rapid Test Kit

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Tetracycline (TCs) Rapid Test Kit

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Sulfonamides (Sas) Rapid Test Kit

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Ciprofloxacin (CPFX) Rapid Test Kit

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Cow Brucella Antibody Rapid Test Kit

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Goat Brucella Antibody Rapid Test Kit

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Aflatoxin Rapid Test Kit (Colloidal gold)

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Dynamiker Monkeypox Virus Ag Rapid Test

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EUR 702
Description: The product is a lateral flow chromatographic immunoassay for the qualitative detection of monkeypox virus antigen in human whole blood, serum, plasma or rash exuudate. The kit is intended for professional use only.

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