Test
IMPACT RPR™ Card Test is a non-treponemal test for the rapid detection and quantitative determination of syphilis in serum or plasma.
Includes | Antigen suspension, dispensing bottle with needle and sheath, pipet/stirrers, Plastic test cards with ten 18mm diameter wells |
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Type | RPR Test Kit |
Detectable Analytes | Detects “reagin” present in serum or plasma of syphilitic patients |
Type | VDRL Flocculation Antigen |
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Product Line | IMPACT RPR™ |
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For large-scale testing in public health and clinical laboratories
For Use With (Application) | For large-scale testing in public health and clinical laboratories |
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Nontreponemal testing procedure for the serologic detection of syphilis
Type | RPR Card Test Kit |
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Formulation | Cardiolipin 0.003%, Lecithin 0.020 to 0.022%, Cholesterol 0.09%, EDTA 0.0125M, Na2HPO4 0.01M, KH2PO4 0.01M, Sodium Azide 0.2%, Charcoal 0.02%, Choline Chloride 10% w/v, Deionized/Distilled Water |
Detectable Analytes | Reagin (Syphilis) |
For Use With (Application) | Serologic detection of Syphilis |
Sure-Vue’s non-treponemal RPR antigen 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. This test is FDA cleared for use in diagnostic screening.
Variation of the standard VDRL
Detectable Analytes | Detects reagin present in Serum of syphilitic patients |
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For Use With (Application) | For in-vitro diagnostic use |
Qualitative and semiquantitative Syphilis screening test
Specificity | >99% |
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Shelf Life | 24 Months |
For Use With (Application) | Syphilis Testing |
The ASI RPR Control Set is used with RPR and VDRL test kits to ensure proper performance. Contains Reacitve, Weak Reactive, and Nonreactive controls.
Includes | Reactive, weak reactive, nonreactive, CLSI package insert |
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Disposable | Single-use |
Type | RPR/VDRL Control Set |
Form | Ready-to-Use (RTU) |
CE Marker | Self-declared |
For Use With (Application) | RPR Test Kit for Syphilis |
Clia Complexity | Moderate (Serum, Plasma or Whole Blood), Waived (Other) |
Used in quality control testing of VDRL Antigen by the slide flocculation test
IMPACT RPR™ Liquid Controls. For use with IMPACT RPR™ test kits.
The ASI VDRL Antigen Test is a non-treponemal test used for the screening of syphilis. VDRL is a specific qualitative (Positive or Negative) and semi-quantitative test (concentration of) that detects reagin antibodies (proteins) in human serum.
Nontreponemal testing procedure for the serologic detection of syphilis
Type | Antigen Suspension |
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Formulation | Cardiolipin 0.003%, Lecithin 0.020 to 0.022%, Cholesterol 0.09%, EDTA 0.0125M, Na2HPO4 0.01M, KH2PO4 0.01M, Sodium Azide 0.2%, Charcoal 0.02%, Choline Chloride 10% w/v, Deionized/Distilled Water |
Detectable Analytes | Reagin (Syphilis) |
For Use With (Application) | Serologic detection of Syphilis |
Determines the presence of reagin antibodies in human serum. It may be used to aid in the diagnosis of syphilis when used in conjunction with supplemental treponemal laboratory tests and other clinical information. Not intended for the screening of blood or tissue donors.