#1038861
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Abbott Rapid Dx North America LLC #435000

Respiratory Test Kit ID NOW™ Respiratory Syncytial Virus Test (RSV) 24 Tests CLIA Waived

Name: Respiratory Test Kit
Brand: ID NOW™

TEST KIT, RSV ID NOW (24/KT)

Abbott Rapid Dx North America LLC 435000

Respiratory Test Kit ID NOW™ Respiratory Syncytial Virus Test (RSV) 24 Tests CLIA Waived

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Product Specifications

McKesson #

1038861

Manufacturer #

435000

Brand

ID NOW™

Manufacturer

Abbott Rapid Dx North America LLC

Country of Origin

United States

Application

Respiratory Test Kit

CLIA Classification

CLIA Waived

CLIA Classified

CLIA Waived

Contents 1

Test Base, Sample Receiver, Transfer Cartridge, Sterile Nasopharyngeal Swab, Positive Control Swab, Negative Control Swab, Plastic Disposable Pipette, Package Insert, Quick Reference Instructions

For Use With

For ID Now™ Instrument US

Number of Tests

24 Tests

Product Dating

McKesson Acceptable Dating: we will ship >= 90 days

Purchase Program Type

Standard Purchase

Reading Type

Machine Read

Sample Type

Nasopharyngeal Swab Sample

Specialty

Molecular

Test Kit Type

Rapid

Test Name

Respiratory Syncytial Virus Test (RSV)

Test Type

Molecular Diagnostic

Time to Results

15 Minute Results

UNSPSC Code

41116144

Features

ID NOW™ RSV detects the RSV virus in nasopharyngeal (NP) swab samples using Alere’s proprietary Molecular In Minutes™ isothermal nucleic acid amplification technology (iNAT)
ID NOW™ i RSV is a rapid (less than 15 minutes), instrument-based isothermal test for the qualitative detection of RSV A and RSV B from nasopharyngeal swabs and nasopharyngeal swabs eluted in viral transport media
It is comprised of a Sample Receiver, containing elution buffer, a Test Base, comprising two sealed reaction tubes, each containing a lyophilized pellet, a Transfer Cartridge for transfer of the eluted sample to the Test Base
The reaction tubes in the Test Base contain the reagents required for amplification of RSV A and RSV B, respectively, as well as an internal control
Intended for use as an aid in the diagnosis of RSV in children <18 years and adults ≥60 years in conjunction with clinical and epidemiological risk factors