Complete System for Autoclave Validation with Six Data Loggers

The AVS140-6 is a complete system that can be used to perform autoclave validations. Equipped with six high temperature and pressure data loggers, an IFC406 Multiplexer Interface and the MadgeTech 4 Secure Software, the AVS140-6 provides users a full range of tools that assist industries ensure compliance with FDA 21 CFR Part 11.

Product Specifications        

More specifically, the AVS140-6 kit consists of:

  • Total weight: 12.00 pounds
  • 5 HiTemp140 High Temperature Data Loggers with 1 in probe style
    • Each data logger comes with their own Calibration Certificates
    • Each of these loggers are rugged and high precision tools that are ideal for use in harsh environments, such as those which exists in autoclaves.
    • Stainless steel loggers
    • Fully submersible
    • Capable of withstanding temperatures as high as 140 °C (284 °F)
    • Accuracy: +/-0.1 °C (0.18 °F)
  • 1 PR140 Pressure Data Logger
    • Also comes with its own Calibration Certificate
    • Designed for use in autoclave validation and mapping procedures
    • Capable of withstanding temperatures as high as 140 °C
    • Completely submersible
    • IP rating of IP68
    • Equipped with a precision stainless steel pressure gauge
    • Accuracy of ±0.03 Bar (±0.435 PSI)
    • Capable of operating in a wide temperature range:
      • 20 °C to +140 °C (68 °F to 284 °F)
    • Reading rate can be as often as one reading/second (1 Hz)
    • Non-volatile memory storage: 32,700 measurements
  • IFC406 Multiplexer interface
  • MadgeTech Secure Data Logger Software
    • Software is equipped with IQ/OQ/PQ validation protocols and workbook
    • Assists customers to ensure their compliance with 21 CFR Part 11 requirements
    • All standards are stored as electronic files that are considered equivalent to paper records, saving time and effort
    • Software contains various important criteria, such as electronic signatures, access codes, secure data files, provide system integrity and an audit trail, all of which meet the FDA 21 CFR Part 11