RPR Card Test for Syphilis

ASI’s nontreponemal (lipoidal antigen) Rapid Plasma Reagin test screens for syphilis; a sexually transmitted disease caused by the bacterium Treponema pallidum (a spirochete bacteria). The disease is found worldwide and is easily treated if detected early. If left untreated it can be fatal and facilitate the transmission and acquisition of HIV.1 This test is FDA cleared for use in diagnostic screening.

Nontreponemal tests, such as the ASI RPR Card Test, are more reliable indicators of untreated syphilis infections and are used to monitor response to treatment or to indicate new infections.2

Features

assignmentA syphilis primary screening test
visibilityEasy to interpret
colorizeColor-coded dropper vials
360Screw cap vials (No glass ampules)
verifiedProven results in proficiency surveys
grid_view10 and 30 well test cards available
attach_moneySimple and economical to use
checklistAll testing materials provided
opacity3 levels of liquid controls included (reactive, weak reactive, nonreactive)
layersWarp resistant coated test cards
scheduleUp to 24 month shelf life (from date of manufacture)
do_not_disturbAvailable without controls
blue American flag
Made in USA
A kit including six small labeled bottles with colored caps, a card with 10 test circles labeled for single use, and a plastic dropper, titled 'Making sure you have all you need. Included in our kits.'Text reading 'Results you can rely on' above two boxes showing '98% SENSITIVITY' and '99% SPECIFICITY' in blue and black text on a light background.A white capped glass vial on the right side with text on the left side saying: Alleviating frustration. Our kits boast a screw cap glass vial making opening smooth and painless, on a blue background.Illustration showing a reagent bottle being opened with a clock and equal sign, next to the text 'Made to last. The expiry date of our reagents stays true even when opened, so you can do more with less.'
Made In USA

Certifications

  • CPT Code 86592 (Screening)
  • CPT Code 86593 (Titers)
  • FDA 510(k) K851504

Sensitivity & Specificity

  • Sensitivity: >98%
  • Specificity: >99%

Test Kit Sizes

  • 25 test kit #900025
  • 100  test kit #900100
  • 500  test kit #900500
  • 5,000  test kit #9005000-10
  • 5,000  test kit #9005000-30
  • 10,000  test kit #90010000-30