Introduction
2067634-131 Revision E
SEER ™ 1000
19
These devices also represent possible causes of interference as they may emit
higher levels of electromagnetic radiation.
NOTICE
FAILURE OF EQUIPMENT - The use of mobile phones and other devices AF in the
periphery of the system may cause unexpected or undesirable behavior.
Avoid the use of mobile phones and other devices nearby AF system.
NOTICE
Attachments or components - The addition of accessories or components to the system
or the device or system modification can lead to an increase of radiation or reduced
immunity of the device or system.
More information about EMS / CEM and AF can be obtained from the following sources:
O Reference Manual of spare parts and accessories
O Reference Manual of spare parts and accessories
for your system
O Or authorized representatives GE Healthcare GE Healthcare
O Or authorized representatives GE Healthcare GE Healthcare
O Annex on electromagnetic compatibility in this manual
O Annex on electromagnetic compatibility in this manual
instructions.
biocompatibility
The system components described in this manual, including accessories that, when used as
prescribed, come in contact with the patient meet the biocompatibility requirements of the
relevant standards. If you have questions about this, please contact GE Healthcare or their
representatives.
Information on spare parts and accessories
Ordering information and a list of products that are approved for use with this device, are in
SEER 1000 -
Reference Manual of spare parts and accessories
which are supplied with each recorder.
Reference Manual of spare parts and accessories
which are supplied with each recorder.