Sciteck™ SVT™ Adulteration Chromate Reagent

For use with automated systems for drugs of abuse adulteration testing

Manufacturer:  Sciteck™ 60003

Catalog No. 23-424-4552

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

• Certifications/Compliance: CAP FDT the Gold Standard, SAMHSA, HHS CLIA
• Intended Use: In-vitro diagnostic use to quantitatively determine the presence of chromates in Urine, forensic/toxicology use
• Source: Human Urine
• Type: Chromate Calibrator, 5mg/dL

• For Use With (Equipment): Automated system for drugs of abuse adulteration testing
• Quantity: 60mL
• Storage Requirements: 2° to 10°C

U.S. and Foreign Patents and Patents Pending