Acteon X-MIND trium - Interactions, Contraindications, and Prohibitions; Interference with Medical Devices; Prohibited Operating Conditions

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USER MANUAL• X-Mind trium • (13) • 03/2018 • NTR0EN010M
ENGLISH
INTERACTIONS
CONTRAINDICATIONS
PROHIBITIONS
This includes information relating to the interactions, contraindications and prohibitions known by ACTEON
Imaging
®
on the date on which this document was written.
13.1 INTERFERENCES WITH OTHER MEDICAL DEVICES
Interferences may occur when the system is used on patients tted with a pacemaker.
The medical device presents potential risks due to the emission of electromagnetic elds.
13.2 USING ACCESSORIES NOT SUPPLIED BY ACTEON IMAGING
®
The medical device was designed and developed with its accessories to guarantee maximum safety and
performance. The use of accessories from another source could put you and your patients at risk and could
damage your medical device. Do not try to connect accessories not provided by ACTEON Imaging
®
to your
medical device.
Even if the manufacturer or dealer of your accessory claims full compatibility with ACTEON Imaging
®
equipment, it
is advisable to exercise caution with regards to the origin and safety of the product offered. Look out in particular
for lack of information, information in a foreign language, very attractive prices, suspect appearance, mediocre
quality or premature wear. If necessary, contact an approved dealer or the ACTEON Imaging
®
Customer Service.
13.3 PROHIBITED USES
• Do not immerse or use outdoors.
• Do not place the medical device next to a source of heat or in direct sunlight.
• Do not expose the medical device to water spray or mist.
A hot/cold temperature contrast can cause condensation to form in the medical device, which may be dangerous.
The medical device may not be stored or used outside the atmospheric pressure and temperature ranges
recommended in the User Manual supplied with your medical device.
Do not touch accessible electrical connections.
13.4 MOVING THE MEDICAL DEVICE
After its initial installation, the medical device is not designed to be moved. The medical device must be xed to
ensure that it cannot be removed or moved without the use of a tool. Do not move the medical device during use.
13.5 ASSEMBLY AND DISASSEMBLY
Unless otherwise indicated in the instructions specic to your medical device:
• Control devices are not designed to be removed or disassembled.
• Access doors and/or aps are not designed to be removed or disassembled.