Product Comparison

  Arlington Scientific 900100 BD 446252 Abbott Rapid Dx North America LLC 7D2648 Sekisui Diagnostics 183 Sekisui Diagnostics 181
McKesson # 889265 365609 875804 548464 548463
Description Sexual Health Test Kit ASI™ Syphilis Screen 100 Tests CLIA Non-Waived Sexual Health Test Kit BD Affirm™ VPIII Candida Species / Gardnerella Vaginalis / Trichomonas Vaginalis 24 Tests CLIA Non-Waived Sexual Health Test Kit Determine™ HIV-1/2 Ag/Ab Combo 25 Tests CLIA Waived Sample Dependent Sexual Health Test Kit OSOM® BVBLUE® Bacterial Vaginosis (BV) 25 Tests CLIA Waived Sexual Health Test Kit OSOM® Trichomonas Vaginalis 25 Tests CLIA Waived
Manufacturer # 9001004462527D2648183181
Brand ASI™BD Affirm™ VPIIIDetermine™OSOM® BVBLUE®OSOM®
Manufacturer Arlington ScientificBDAbbott Rapid Dx North America LLCSekisui DiagnosticsSekisui Diagnostics
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CLIA Classification CLIA Moderate ComplexityCLIA Non-WaivedCLIA Waived for Fingerstick Whole Blood / CLIA Moderate Complexity for Venous Whole Blood, Serum, PlasmaCLIA WaivedCLIA Waived
CLIA Classified CLIA Non-WaivedCLIA Non-WaivedCLIA Waived Sample DependentCLIA WaivedCLIA Waived
Contents 1 RPR Carbon Antigen, Reactive Control, Weak Reactive Control, Nonreactive Control, 3 mL Dropping Bottle, 20 ga. Dispensing Needle (60 drops/ml), RPR Test Card (10-well), 0.05 mL Stirrer Pipets(24) Probe Analysis Cards, (24) Reagent Cassettes, 3.4 mL Substrate Solution, 10.8 mL Lysis Solution, 15 mL Buffer Solution, (24) Filter Tips, (24) Sample Collection Cups, (24) Sample Collection Tubes, (24) Sterile Swabs(25) Test Cards, Chase Buffer, Package Insert, Quick Reference Guide, (25) Capillary Tubes, (25) Disposable Workstations(25) Test Vessels, Bottle Developer Solution, Sterile Swabs, Directional Insert(25) Test Sticks, (25) Sterile Swabs, (25) Test Tubes, 25 mL Sample Buffer, Sample Buffer Dropper Top, Positive Control Swab, Workstation, Directional Insert, Extra Swabs and Tubes also Provided
Country of Origin United StatesPuerto RicoUnited StatesUnited StatesUnited States
Number of Tests 100 Tests24 Tests25 Tests25 Tests25 Tests
Product Dating McKesson Acceptable Dating: we will ship >= 60 daysMcKesson Acceptable Dating: we will ship >= 60 daysMcKesson Acceptable Dating: we will ship >= 90 daysMcKesson Acceptable Dating: we will ship >= 90 daysMcKesson Acceptable Dating: we will ship >= 90 days
Sample Type Serum / Plasma SampleVaginal Secretion SampleWhole Blood / Serum / Plasma SampleEndocervical SampleVaginal Secretion Sample
Specialty MicrobiologyMicrobiologyImmunoassayMicrobiologyImmunoassay
Storage Requirements Requires RefrigerationRequires RefrigerationRequires Refrigeration
Technology Lateral Flow
Test Format Test Card FormatTest Card FormatTest Card FormatTube FormatDipstick Format
Test Kit Type RapidStandardRapidRapidRapid
Test Method Lateral Flow Method
Test Name Syphilis ScreenCandida Species / Gardnerella Vaginalis / Trichomonas VaginalisHIV-1/2 Ag/Ab ComboBacterial Vaginosis (BV)Trichomonas Vaginalis
Test Type RPR Card TestMicrobial IdentificationAntibody / Antigen TestEnzyme Activity TestInfectious Disease Immunoassay
Time to Results 8 Minute Results45 Minute Results20 Minute Results10 Minute Results10 Minute Results
UNSPSC Code 4111612941116129411161444111612941116129
Application Sexual Health Test KitSexual Health Test KitSexual Health Test KitSexual Health Test KitSexual Health Test Kit
Purchase Program Type Standard PurchaseStandard PurchaseStandard PurchaseStandard PurchaseStandard Purchase
Reading Type Visual ReadVisual ReadVisual ReadVisual ReadVisual Read
Features and Benefits
  • The ASI RPR (rapid plasma reagin) Card Test for syphilis is a qualitative and semiquantitative nontreponemal flocculation test for the detection of reagin antibodies in human serum and plasma as a screening test for serological evidence of syphilis
  • All testing materials provided
  • 3 levels of liquid controls included: reactive, weak reactive, nonreactive
  • Color-coded dropper vials
  • Warp resistant coated test cards
  • Screw cap vials - no glass ampules
  • The Affirm™ VPIII Microbial Identification Test is a DNA probe test intended for use in the detection and identification of Candida species, Gardnerella vaginalis and Trichomonas vaginalis nucleic acid in vaginal fluid specimens
  • The test uses two distinct single-stranded nucleic acid probes for each organism, a capture probe and a color development probe, that are complementary to unique genetic sequences of the target organisms
  • The capture probes are immobilized on a bead embedded in a Probe Analysis Card (PAC), which contains a separate bead for each target organism
  • The color development probes are contained in a multi-well Reagent Cassette (RC)
  • Kit includes: 24 Probe Analysis Cards (PAC), 24 Reagent Cassettes (RC), 3.4 mL Substrate Solution, 10.8 mL Lysis Solution, 15 mL Buffer Solution, 24 Filter Tips, 24 Sample Collection Cups, 24 Sample Collection Tubes, 24 Sterile Swabs
  • Individually packaged cards, wrapped in an absorbent paper towel moistened with a solution containing sodium azide (0.1%, w/v) as a preservative
  • Each PAC contains the following five beads: Negative Control, Trichomonas, Gardnerella, Candida, and Positive Control
  • Reagents are sealed in multi-well, foil covered cassettes
  • Each cassette has seven wells
  • All reagents are supplied ready for use
  • Innovative: The first and only FDA cleared point-of-care test that detects both HIV-1/2 antibodies and free HIV-1 p24 antigen on single test strip
  • CLIA Waived (Fingerstick Collection): 3 easy steps and minimal training to allow testing across a range of test sites
  • Proven: 99.9% overall clinical sensitivity for all sample types
  • Rapid: Results in just 20 minutes
  • Flexible Sample Types: Test using capillary and venous whole blood, serum, and plasma
  • Each test strip has a cover that is to be removed for sample application and visualization of test results
  • Detects elevated vaginal fluid sialidase activity, an enzyme produced by bacterial pathogens associated with bacterial vaginosis including Gardnerella, Bacteroides, Prevotella and Mobiluncus
  • The OSOM® Trichomonas Rapid Test is intended for the qualitative detection of Trichomonas vaginalis (Trichomona) antigens from vaginal swabs or from the saline solution prepared when making wet mounts from vaginal swabs
  • Accurate - 95 percent agreement against composite reference standard (culture and wet mount)
  • Provides easy-to-read two color results
  • Room Temperature Storage - 16 month shelf life
  • The OSOM® Trichomonas Rapid Test is an immunochromatographic assay that detects pathogen antigens directly from vaginal swabs