8
March
2017
8818 User Guide
(BB1505-H)
Changing Frequency
The Multi-Frequency Imaging (MFI) facility enables you to select the imaging
frequency. See the applicable system user guide for instructions. The selected
frequency is displayed at the top of the screen.
Using a Transducer Cover
The transducer should be enclosed in a transducer cover or a standard condom. See
the Product Data sheet for a list of available transducer covers.
Apply sterile gel to the tip of the transducer or fill the cover with 1 to 2 ml of sterile
water. This improves the screen images by preventing image artifacts caused by air
bubbles.
Pull the transducer cover over the transducer.
Gel also creates a good acoustic contact between the skin and the transducer;
therefore, apply a small amount to the outside of the cover prior to imaging. Re-apply
the gel frequently to ensure good screen images.
Using the Transducer Control Button
To change the imaging plane, press the button corresponding to that plane (see Figure
1). Pressing the button activates (starts) or freezes (stops) imaging in that plane. One
button enables the sagittal or longitudinal array. A long press on this button also
activates endfire imaging. A second button enables the transverse array. Each time a
button is pressed, a beep is emitted.
Changing Orientation
To change the orientation of the image on the monitor, refer to the applicable system
user guide for instructions.
WARNING
Because of reports of severe allergic reactions to medical devices containing latex ( natural
rubber), FDA is advising health-care professionals to identify their latex-sensitive patients
and be prepared to treat allergic reactions promptly.
WARNING
Use only water-soluble agents or gels. Petroleum or mineral oil-based materials may harm
the cover materials.
WARNING
Do not use excessive force during insertion. Do not make excessive lateral movements
during or after insertion. Risk of injury or tissue damage to the patient could occur under
certain circumstances. A digital palpation of the rectum may need to be carried out by a
clinician prior to insertion or use of the probe as a precautionary measure.
