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DPP® HIV-1/2 Antibody Sexual Health Test Kit #65-9500-0

DPP®

$229.66
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DPP® HIV-1/2 Antibody Sexual Health Test Kit #65-9500-0
  • DPP HIV 1/2 Assay uses Next Generation DPP™ technology which offers excellent sensitivity and specificity.
  • Patient friendly foam swab.
  • The DPP SampleTainer bottle is a safe, closed system for handling potentially infectious blood and oral fluid samples.
  • Approved to detect HIV in patients 2 years old and older.
  • Documentation included: 20 copies of subject information notice, quick reference instructions (for CLIA waived), a product insert for the DPP HIV 1/2.
SKU:
944104
Contents:
(20) Test Devices, (20) Swabs, (20) Sample Loops, (20) Specimen Container Bottles, Running Buffer, Quick Reference Instructions, (20) Subject Information Notices, Product Insert
QTY Per Sell:
20
Number of Tests:
20 Tests
Reading Type:
Visual Read
Sample Type:
Whole Blood / Serum / Plasma / Saliva Sample
Manufacturer:
Chembio Diagnostic Systems, Inc.
Manufacturer Link:
li>Chembio Diagnostic Systems: https://www.chembio.com
Regulatory Information:
li>FDA PMA BP120032; approved Dec 19, 2012
  • GUDID GS1 Device ID: 00607158000007
    • CLIA Classification:
    CLIA Waived (point-of-care use in CLIA waived settings).
    Intended Use:
    li>Point-of-care rapid qualitative assay to aid diagnosis of HIV-1 and HIV-2
    Package Insert / Docs:
    li>Package Insert (FDA listing) provided with kit
    SKU:
    944104
    Contents:
    (20) Test Devices, (20) Swabs, (20) Sample Loops, (20) Specimen Container Bottles, Running Buffer, Quick Reference Instructions, (20) Subject Information Notices, Product Insert
    QTY Per Sell:
    20
    Number of Tests:
    20 Tests
    Reading Type:
    Visual Read
    Sample Type:
    Whole Blood / Serum / Plasma / Saliva Sample
    ic__sync_id:
    1
    ic__id:
    1270
    Manufacturer:
    Chembio Diagnostic Systems, Inc.
    Manufacturer Link:
    li>Chembio Diagnostic Systems: https://www.chembio.com
    Regulatory Information:
    li>FDA PMA BP120032; approved Dec 19, 2012
  • GUDID GS1 Device ID: 00607158000007
    • CLIA Classification:
    CLIA Waived (point-of-care use in CLIA waived settings).
    Intended Use:
    li>Point-of-care rapid qualitative assay to aid diagnosis of HIV-1 and HIV-2
    Package Insert / Docs:
    li>Package Insert (FDA listing) provided with kit