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Endocavity/General Purpose Probe Disinfection & Storage
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  • Description:

trophon2 is the latest innovation in ultrasound probe high level disinfection. It features enhancements in integrated traceability and user experience.

Smart User Experience

Gain access to a host of Smart Functionality with trophon2 and perform the HLD process simply, automatically, and with confidence.

  • Large, 7" color touchscreen with simple animations to navigate you through the disinfection process
  • Programmable – Imagine no waiting for warm-up; simply pre-program for daily start-up before the first scheduled patient
  • Quiet disinfection cycle – Use trophon2 right in the scan room with no impact on the patient experience
  • Easy probe loading – Easy-load clamp, integrated positioner and probe cable tray reduce the potential for probe damage

Smart Traceability

AcuTrace™ is an automated HLD traceability system that incorporates RFID (Radio Frequency Identification Technology). AcuTrace-enabled accessories and consumables contain RFID chips that store digital information and can be read by the built-in AcuTrace reader.

  • It simplifies the creation of accurate, audit-ready digital records – all stored on your trophon2
  • Automated trophon2 ensures consistent and reproducible HLD to help you meet ultrasound probe HLD guidelines and standards ¹¯³

References: 1. Rutala WA, Weber DJ, HICPAC. Guideline for Disinfection and Sterilization in Healthcare Facilities. USA: Centers for Disease Control; CDC 2008. (https://www.cdc.gov/infectioncontrol/pdf/guidelines/disinfection-guidelines.pdf).

2.Electronically accessed: Joint Commission Alert is Another Wake-Up Call for Awareness of Improper HLD or Sterilization. http://www.infectioncontroltoday.com/articles/2014/08/joint-commission-alert-is-a-another-wakeup-call-for-awareness-of-improper-hld-or-sterilization.aspx.

3.U.S. Department of Health and Human Services, Food and Drug Administration (FDA), Center for Devices and Radiological Health (CDRH), Office of Device Evaluation, Center for Biologics Evaluation and Research (CBER). Reprocessing Medical Devices in Health Care Settings: Validation Methods and Labeling. Guidance for Industry and Food and Drug Administration Staff. March 17, 2015.

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