trophon®2
| E8350MA | |
| New | |
| Ultrasound | |
| Endocavity/General Purpose Probe Disinfection & Storage | |
| Nanosonics | |
| GE Precision Healthcare | |
| GE HealthCare | |
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Product Overview
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.
Return And Exchange
GE HealthCare will accept, for return from customer, items that are in new condition, unworn, unaltered and free of damage. Items cannot be returned or exchanged beyond 30 days from customer’s receipt of the original order and all returned items will be subject to a 15% restocking fee. To obtain a full refund or exchange of the item within the 30 day return period (subject to the 15% restocking fee) customer must request a return materials authorization (RMA) from GE HealthCare and return the item to GE HealthCare utilizing this RMA number. Items must be returned in the original packaging, unused and free of damage.
Please note, cuffs, BP items clinical accessories, sterile and hazmat items cannot be returned. If a replacement order is requested, the restocking fee may be waived at GE HealthCare’s sole discretion.
