Philips iU22 - Patient-Contact Parts; Preventing Intraoperative Transducer Problems

WARNINGS
•
All intraoperative studies must be performed with a Type CF classified
transducer. If your transducer is not labeled Type CF on the transducer
connector, contact your Philips service representative.
• Be sure to use a market-approved sterile transducer cover and sterile
ultrasound transmission gel when performing all intraoperative studies.
• Always remove the transducer from the patient before defibrillation.
Patient-Contact Parts
Latex is commonly used in sheaths marketed to help with infection control in
transesophageal, endocavity, and intraoperative imaging applications and during
biopsies. Examine the packaging to confirm latex content. Studies have shown
that patients can experience allergic reactions with natural rubber latex. See
"FDA Medical Alert on Latex" on page 45.
NOTE
The ultrasound system and transducers discussed here do not contain natural
rubber latex that contacts humans. Natural rubber latex is not used on any Philips
ultrasound transducers.
Preventing Intraoperative Transducer Problems
WARNING
If you find any signs of damage to the transducer, patient safety may be
compromised. Do not use the transducer, and contact your Philips service
representative.
Meticulous inspection and correct and careful operation of intraoperative
transducers are imperative to patient safety. The situations listed here affect safe
operation as well as the ability to service mechanical problems under the Philips
warranty or service contract. Transducer repairs necessitated by misuse are not
covered and can be very costly, often requiring complete disassembly and
rebuilding of the transducer.
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iU22 User Manual
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Intraoperative Transducers