om 5184516-100 Rev. 5 2-5
The medical staff in charge of this equipment is required to instruct technicians,
patients, and other people who may be around this equipment to fully comply with
the above requirement.
This product complies with the regulatory requirements of the following:
• Council Directive 93/42/EEC concerning medical devices when it bears the
following CE marking of conformity:
High levels of Radio Frequency (RF) energy in the vicinity of this X–
Ray Suite may cause noise to appear on video monitors and
recorders. This noise should disappear spontaneously when the
stimulus is removed. If the problem persists, call Service.
Under certain Electro Static Discharge (ESD) and Electrical Fast
Transient (EFT) conditions, noise may appear on video monitors and
recorders. This noise should disappear spontaneously when the
stimulus is removed. If the problem persists, call Service.
Under certain conditions, ESD may cause temporary anomalies to be
present on the image monitors and the VCR. This is a temporary
degradation during the ESD event and does not cause any system
issues.
Under certain conditions, transients on the power line may cause
temporary anomalies to be present on the image monitors. This is a
temporary degradation during the transient event and does not cause
any system issues.
FOR TRAINING PURPOSES ONLY!
NOTE: Once downloaded, this document is UNCONTROLLED, and therefore may not be the latest revision. Always confirm revision status against a validated source (ie CDL).
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