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Sciteck™ SVT™ Adulteration Chromate Reagent

For use with automated systems for drugs of abuse adulteration testing

Manufacturer:  Sciteck™ 60004

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Catalog No. 23-424-4555


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Description

Description

  • 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

Specifications

Specifications

CAP FDT the Gold Standard, SAMHSA, HHS CLIA
In-vitro diagnostic use to quantitatively determine the presence of chromates in Urine, forensic/toxicology use
Human Urine
Chromate Calibrator, 50mg/dL
Automated system for drugs of abuse adulteration testing
60mL
2° to 10°C
SDS
Documents
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