Sciteck™ SVT™ Adulteration Chromate Reagent

For use with automated systems for drugs of abuse adulteration testing

Manufacturer: SCITECK DIAGNOSTICS INC 600

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Catalog No. 23-424-4551

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    Specifications

    Product Type Chromate Reagent R(1)
    Source Human Urine
    For Use With (Application) In-vitro diagnostic use to quantitatively determine the presence of chromates in Urine, forensic/toxicology use
    For Use With (Equipment) Automated system for drugs of abuse adulteration testing
    Storage Requirements 2° to 10°C
    Quantity 750mL

    • For in vitro diagnostic use to detect presence of chromates in solution
    • Analysis based on an indicator reaction which gives a change of absorbance in presence of chromates
    • May be used on any freshly voided urine specimen or urine collected under special circumstances (e.g. first-morning specimens, post-prandial urine)
    • Use with Zero Calibrator (23-424-4545)

    Sciteck™ Specimen Validity Testing (SVT™)

    • In accordance with SAMHSA's FWDTP guidelines as specified by Executive Order 12564 and delineated in the Federal Register Vol. 53 FR 11970-11989 and Vol. 59 FR 29908-29931; and other federally mandated programs (DOT, DOE, NRC and FHWA) for employment drug screening
    • Sciteck evolved from Chimera Research, providing liquid reagents to laboratories for specimen validity testing in urine specimens submitted for DAU testing since 1989
    • Adulteration testing products to include extensive SVT adulteration and EIA™ Drugs of Abuse single and multi-assay(s) (4-in-1™) reagent line
    • SVT line consists of assays for pH, specific gravity, nitrite (non-corrosive), aldehydes, oxidants, chromate, creatinine, and halogens (bleach)
    • AdultaCheck™ for on-site adulteration products

  • Description & Specifications

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