The QbD1200 TOC analyzer is designed to make testing easier, reproducible and accurate. The new TOC analyzer promises highest performance while dramatically reducing cost of ownership by using one reagent for the test and requiring only one annual service call rather than frequent maintenance. The new TOC analyzer eliminates the dependency on lengthy overnight routines that may fail. In the first of its kind the QbD1200 TOC analyzer calibrates in only 90 minutes. The QbD1200 is designed for use in 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 file and provides paperless reporting to distribute all auditable reports over secure protocol to a central server.

Specifications

Platform Anatel
Detection Digital NDIR Detector (limit: 0.4ppb)
Reporting Reporting Units: μg/L (ppb)
Industry Standards 21 CFR Part 11, USP <643> (including Sterile Water SST), JP-16 <2.59>, EP <2.2.44>, IP, CP, KP, US EPA 5310c, ICH guidelines for instrument validation included in IQ/OQ
Display 10.4" high-resolution color touch screen
Operating System Paperless reporting via secure FTP over Ethernet
Humidity Restrictions Up to 90% relative humidity (non-condensing)
Temperature Range Operating temperature range: 10°C to 35°C
Power Requirements 47-63 Hz, 100-240 VAC
Additional Information Light source: UV Lamp confirmation: Broadband silicat photodiode sensor

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.