دستگاه اتوکلاو زمینی آزمایشگاهی از شرکت Systecآلمان - Horizontal, Floor standing Systec Autoclave

Standard Features HX

Integrated, separate steam generator

Housing, support frame and pressure vessel made of corrosion-resistant stainless steel

Temperature and pressure range 140 °C, 4 bar

Touch-Screen control

Number of sterilization programs up to 100

Code-secured access rights for changing parameters and further safety-relevant intervention

Internal memory for storing up to 500 sterilization cycles

Timer for starting programs

Autofill: automatic demineralized water feed for steam generation

Flexible PT-100 temperature sensor

Additional temperature sensor in condense exhaust

Temperature holding function for liquids after program finish

Special program for Durham tubes

Calculation of F0 value

Special program for waste sterilization with
pulsed heat-up for more efficient air exhaust

Water-cooled steam exhaust, thermostatically controlled

Programmable automatic door-opening on completion of program

RS-232 and RS-485 interfaces for external data transmission
(network-compatible)

Available options

Extension of temperature and pressure ranges to 150 °C / 5 bar
(from chamber volume 65 liters to 650 liters)

Options for process optimization

Rapid cooling for efficient and safe cooling of liquids

Vacuum system for validatable sterilization of solids and waste materials in disposal bags

Superdry: for drying solids
(only in combination with optional vacuum system)

Exhaust filtration (including condensate inactivation)
for safe sterilization of hazardous biological substances

Options for documentation

Integrated printer for batch documentation

PC software for comprehensive documentation

Comlog: includes USB – and Ethernet-Connection and internal memory for up to 10,000 sterilization cycles, including documentation software on Comlog. The software can be called up independent of platform (PC, laptop, tablet, smart phone), facilitating remote service

AuditTrail: unalterable and traceable documentation acc. to FDA 21 CFR Part 11