Salocor Covid-19 Antigen Test

$0.00
  • Tests for Covid-19

  • Formerly Sienna (Same test!)

  • Results in 10 minutes

  • Lower nasal swab

  • 87.5% PPA, 98.9% NPA

  • Long-dated expiration

Add To Cart
  • Tests for Covid-19

  • Formerly Sienna (Same test!)

  • Results in 10 minutes

  • Lower nasal swab

  • 87.5% PPA, 98.9% NPA

  • Long-dated expiration

  • Tests for Covid-19

  • Formerly Sienna (Same test!)

  • Results in 10 minutes

  • Lower nasal swab

  • 87.5% PPA, 98.9% NPA

  • Long-dated expiration

Specifications

  • CLIA Waived

  • Test type: Rapid Antigen

  • Run time: 10 minutes

  • Collection type: Nasopharyngeal swab

  • Covid: 87.5% PPA, 98.9% NPA

  • CPT Codes: Covid-19 87811QW

  • Manufacturer: Salofa Oy (Finland)

Storage & Expiration

  • Store at 2-30°C (35-86°F)

  • Do not freeze any contents of the kit.

  • Reagents and materials are stable until expiration date printed on outer packaging.

  • Test device must remain in the sealed pouch until use.

Box Components

  • Nasopharyngeal swabs (25)

  • Test cassettes (25)

  • Extraction buffer tubes (25)

  • Workstation for mass testing (1)

  • Positive control swab (1)

  • Negative control swab (1)

  • Instructions for use (1)

  • Quick User Guide (1)

Manuals & Documents

Intended Use

The Salocor COVID-19 Antigen Rapid Test Cassette is a lateral flow immunoassay intended for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct anterior nasal swab specimens from individuals who are suspected of COVID-19 by their healthcare provider within the first five (5) days of symptom onset. Anterior nasal swab specimens may be collected by a healthcare provider (HCP) or self-collected (by individuals 18 years of age or older, under the supervision of an HCP). Testing is limited to laboratories certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. §263a, that meet the requirements to perform moderate complexity, high complexity, or waived tests. This test is authorized for use at the Point of Care (POC), i.e., in patient care settings operating under a CLIA Certificate of Waiver, Certificate of Compliance, or Certificate of Accreditation.