GE LOGIQ 7 Pro Quick Manual page 49

LOGIQ 7/LOGIQ 7 Pro Quick Guide
EMC (Electromagnetic Compatibility)
NOTE: This equipment generates, uses and can radiate radio frequency energy. The equipment may cause radio frequency interference to other medical and non-
medical devices and radio communications. To provide reasonable protection against such interference, this product complies with emissions limits for a Group 1,
Class A as stated in IEC/EN 60601-1-2:2001. However, there is no guarantee that interference will not occur in a particular installation.
NOTE: If this equipment is found to cause interference (which may be determined by turning the equipment on and off), the user (or qualified service personnel)
should attempt to correct the problem by one or more of the following measure(s):
• reorient or relocate the affected device(s)
• increase the separation between the equipment and the affected device
• power the equipment from a source different from that of the affected device
• consult the point of purchase or service representative for further suggestions.
NOTE: The manufacturer is not responsible for any interference caused by using other than recommended interconnect cables or by unauthorized changes or
modifications to this equipment. Unauthorized changes or modifications could void the users' authority to operate the equipment.
NOTE: To comply with the regulations on electromagnetic interference for a Group1/Class A, all interconnect cables to peripheral devices must be shielded and
properly grounded. Use of cables not properly shielded and grounded may result in the equipment causing radio frequency interference in violation of the
regulations.
NOTE: Do not use devices which intentionally transmit RF Signals (cellular phones, transceivers, or radio controlled products) other than those supplied by GE
(wireless microphone, for example) in the vicinity of the equipment as it may cause performance outside the published specifications. Keep the power to these type
devices turned off when near this equipment.
The medical staff in charge of this equipment is required to instruct technicians, patients, and other people who maybe around this equipment to fully comply with the
above requirement.
Safety
Direction 5307393-100 Rev. 1 45