Siemens MAGNETOM Skyra fit Operator's Manual page 29

Interferences
Labeling
MR Safe
MAGNETOM Skyra fit | syngo MR E11
Print No. M6-04401.621.02.02.02
Auxiliary equipment, which has not been specifically tested and
approved for use in the environment of the MR equipment, may
result in burns or other injuries to the patient.
If the MR system is combined with other systems or components, it
must be ensured that the planned combination and cable routing do
not affect the safety of patients, personnel, or the environment.
Ensure that the devices used in the examination room are

compatible with the field strength of the MR system. For
example, devices compatible with 1.5 T systems may be
unsuitable for 3 T systems, and vice versa. See also MR
Conditional: (
◆ Contact Siemens Service prior to combining the MR system with
other devices.
Peripheral equipment (e.g. patient monitoring, life support or
emergency care equipment) which is not specified or recommended
for use in the MRI environment, including the controlled access area,
may be disturbed by the RF field or the magnetic fringe field of the
MR system. This equipment may also disturb the proper function of
the MR system.
ASTM International developed a new classification system for
implants and ancillary clinical devices. The following definitions
apply:
An item that poses no known hazards in all MR environments. MR Safe items
include nonconducting, nonmagnetic items such as a plastic petri dish. An
item may be determined to be MR Safe by providing a scientifically based
rationale rather than test data.
Page 29 Labeling)
Safety 2
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