KTO: PAT700 TOC with Quick Connect FTG
|Industry Standards||USP <643> (including Sterile Water SST), EP <2.2.44>|
|Calibration Intervals and Options||3-point TOC calibration; Conductivity calibration to USP<645>; System suitability to USP, EP and JP|
|Fluid Compatibility||Purified water, Water for injection (WFI)|
|Online Operation||Sample inlet pressure 10 to 100psi (0.69 to 6.89Bar)|
|Reporting||ppb TOC │ mS/cm|
|Temperature Range||5°to 95°C sample range|
|Power Requirements||100/230VAC ± 10%, 65W, 50/60Hz|
|Operating System||Paperless reporting via secure FTP over Ethernet|
|Display||Full-color LCD touch screen|
|Operating Modes||Online TOC; Online Conductivity; Auto-switching Main and Standby UV lamps for 12 months operation │ 4-bottle auto-sampler for grab sample analysis │ Excursion capture for root cause analysis support|
|Weight||13.6 kg / 30 lb|
|Width||59.7 cm / 23.5 in|
|Depth||22.9 cm / 9 in|
|Height||25.4 cm / 10 in|
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.