Important information
4990113_030_01 — 2069106 — 2017–11–02
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1.4.4
MRI safety information
Tests have confirmed that the operating table column Hybrid MR is
MR conditional to the MR environment with the approved operating
tabletops and the cable remote control TS 7500 (#2003862) and
can be used safely for MRI up to a maximum of 3 Tesla.
1.4.5
Maintenance/Repair
• It is prohibited to position a patient on the operating table if the
table is undergoing maintenance or repair.
• Keep a log book for this medical equipment! All repairs and
maintenance are documented here.
• Every repair must comply with the safety regulations according
to IEC 60601-1 (DIN EN 60601-1/VDE 0750-1) and
DIN EN 62353 (VDE 0751-1).
• Within the limits of the legal requirements, the manufacturer is
only responsible for the technical safety characteristics of this
device, if the maintenance, repairs and modifications to this
apparatus are performed by Trumpf Medical service technicians
or by personnel authorized and trained by Trumpf Medical.
• Trumpf Medical will not be held liable for damage of any kind
arising from the failure to perform inspections or as a result of
inadequate maintenance, or of modifications to the product.
CAUTION
Failure to observe the specific procedures for handling
MR conditional products can result in injury to persons
involved.
Please observe the following points to ensure safety in an MRI
environment:
– Please observe the MRI safety information for the operating
table top, the shuttle and the remote control.
– Only use pads specifically designed for the operating table top
(MR safe).
– Do not use the operating tabletop with the MRI until the shuttle
has been transferred to the operating table column (MR
conditional).
– Hang the remote control on the side rail of the operating
tabletop by the “PLACE PENDANT HERE” sticker (MR
conditional).
– Remove the shuttle from the room immediately after the
operating tabletop has been transferred (MR Unsafe).
– Only use authorized accessories.
– It is essential to follow the safety guidelines of the MR device
manufacturer.
