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The new QbD1200 TOC analyzer is designed to make testing easier, reproducible and accurate. The new TOC analyzer eliminates the dependency on lengthy overnight routines that may fail. The QbD1200 TOC analyzer calibrates in only 90 minutes, the first analyzer in the industry that can make this claim. The QbD1200 is designed for 21 CFR part 11 lab environments and is fully compliant with all global pharmacopeia regulations. It offers convenient validation as it is not operated by a separate PC, eliminating the need for an additional CSV fil/, and provides paperless reporting to distribute all auditable reports over secure protocol to a central server. The TOC analyzer promises highest performance while dramatically reducing cost of ownership by using one reagent for the test and requires only one service call per year.
NOT ALL PRODUCTS ARE AVAILABLE IN ALL COUNTRIES
PRODUCT AVAILABILITY AND REGULATORY STATUS DEPENDS ON COUNTRY REGISTRATION PER APPLICABLE REGULATIONS
The listed regulatory status for products correspond to one of the below:
IVD: In Vitro Diagnostic Products. These products are labeled "For In Vitro Diagnostic Use."
ASR: Analyte Specific Reagents. These reagents are labeled "Analyte Specific Reagents. Analytical and performance characteristics are not established."
CE: Products intended for in vitro diagnostic use and conforming to European Directive (98/79/EC). (Note: Devices may be CE marked to other directives than (98/79/EC)
RUO: Research Use Only. These products are labeled "For Research Use Only. Not for use in diagnostic procedures."
LUO: Laboratory Use Only. These products are labeled "For Laboratory Use Only."
No Regulatory Status: Non-Medical Device or non-regulated articles. Not for use in diagnostic or therapeutic procedures.
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