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Brands BD Veritor™ System

Respiratory Test Kit BD Veritor™ System SARS-CoV-2 / Influenza A + B 30 Tests CLIA Waived

Product # : 1192774 Class : MCKSN Distributor : RELIANCE INC Category : Test Kits Availability : Stocked

$0.00

Product Notices : This product may be non-returnable and/or require additional restocking fee.
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Product Specifications

Product No. # 1192774
Manufacturer # 256088
Brand BD Veritor™ System
Manufacturer BD
Country of Origin China
Application Respiratory Test Kit
For Use With For use with the BD Veritor™ Plus Analyzer running Firmware version 5.50 or late
Number of Tests 30 Tests
Sample Type Nasal Swab Sample
Shipping Width 8
Shipping Height 6
Shipping Depth 10
Dimension UOM IC
Shipping Weight 1.6
Weight UOM LB
For_Use_With For use with the BD Veritor™ Plus Analyzer running Firmware version 5.50 or late
QTY_Per_Sell 1
Simply_Medical_Category Test Kits
Reading_Type Machine Read
Supply_Manager_Category Test Kits
Supply_Manager_Hierarchy Clinical Laboratory>Test Kits>Respiratory Test Kit
Legend_Code Yes
Stock_Status Stocked
Velocity Fast Selling
GTIN 00382902560883
Country of Origin China
Ready to Sell Ready to sell
Features
  • The BD Veritor System for Rapid Detection of SARS-CoV-2 and Flu A+B is intended for use in point of care settings by trained healthcare professionals or other users specifically instructed in the use of BD Veritor Systems and proper infection control procedures.
  • Time to result: 15 minutes, test device can be read at 15 minutes but no later than 20 minutes.
  • This product has been authorized only for the detection of proteins from SARS-CoV-2, influenza A and influenza B, not for any other viruses or pathogens.
  • BD Triplex assay requires Veritor™ System firmware version 5.5 or later; firmware version info is displayed on screen when turning on the analyzer or on the orange sticker if it is attached to the analyzer.
  • 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 certified under the Clinical Laboratory Improvement Amendments of 1988 (CLIA), 42 U.S.C. §263a, that meet the requirements to perform moderate, high or waived complexity tests.