• Do not allow water or other liquids to drip onto the transducer connector, the interior of
the system, or the keyboard.
• Maintain a sterile field.
WARNING
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.
WARNING
Be sure to use a market-approved sterile transducer cover and sterile ultrasound
transmission gel when performing all intraoperative studies.
WARNING
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 49
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.
Patient Safety During Intraoperative Studies
Intraoperative Transducers
EPIQ 7 User Manual 4535 617 25341
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Summary of Contents for epiq 7
Page 4: ...4 EPIQ 7 User Manual 4535 617 25341 ...
Page 26: ...Read This First Recycling Reuse and Disposal 26 EPIQ 7 User Manual 4535 617 25341 ...
Page 94: ...DVD RW Drive System Overview System Components 94 EPIQ 7 User Manual 4535 617 25341 ...
Page 154: ...Customizing the System Custom Procedures 154 EPIQ 7 User Manual 4535 617 25341 ...
Page 172: ...Performing an Exam Ending an Exam 172 EPIQ 7 User Manual 4535 617 25341 ...
Page 298: ...System Maintenance For Assistance 298 EPIQ 7 User Manual 4535 617 25341 ...