The PAT700 TOC analyzer fully complies with all global pharmacopeias (USP, EP, JP) requirements. Each sample is fully oxidized guaranteeing the most accurate TOC result that follows EP2.2.44 guidelines. Production uptime is assured with the PAT700 main and standby dual UV lamp design, making it the ideal choice for on-line TOC release. Save time and money - the PAT700 can be installed online and run up to 4 grab samples offline.

Specifications

Platform Anatel
Fluid Compatibility Purified water
Industry Standards USP <643> (including Sterile Water SST), EP <2.2.44>
Power Requirements 50/60 Hz
Installation Category II
Additional Information 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

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.