Moog Curlin 6000 CMS IOD User Manual page 17

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e bolus/data connector is to be used by the patient only for the connection of the bolus
cord with remote switch. Other accessory equipment connected to this digital interface must
be certi ed to the respective IEC/EN standards (i.e. IEC 950 for data processing equipment
and EN 60601-1 for medical equipment.) Furthermore, all con gurations shall comply with
the system standard EN 60601-1. Anyone who connects additional equipment to the signal
input part or signal output part con gures a medical system, and is therefore, responsible that
the system complies with the requirements of the system standard EN 60601-1. If in doubt,
consult the technical services department or your local Moog representative.
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e Moog Curlin Infusion pump has been tested and found to comply with the European
Standard EN 60601-1-2:1993 and EN 60601-2-24:1994.
reasonable protection against harmful interference in a typical medical installation.
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is equipment generates, uses, and can radiate radio frequency energy and, if not installed
and used in accordance with the instructions, may cause harmful interference to other devices
in the vicinity. However, there is no guarantee that interference will not occur in a particular
installation. If this equipment does cause harmful interference to other devices, which can be
determined by turning the equipment o and on, the user is encouraged to try to correct the
interference by one of more of the following measures:
1. Reorient or relocate the receiving device.
2. Increase the separation between the equipment.
3. Connect the equipment into an outlet on a circuit di erent from that to which the
other device(s) are connected.
4. Consult the manufacturer or eld service technician for help.
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Prior to programming Load Dose, refer to Important Information in the appropriate
erapy chapters.
Note: For information regarding the clinician access code, read the chapter entitled "Clinician
Information and Access Code." When entered correctly, the access code allows a user to
change the lock settings of the pump and thereby change the settings of the pump.
Because the chapter entitled "Clinician Information and Access
I M PORTAN T
Code" contains access code information, the entire chapter should be
I N FORM AT I ON
removed before initial patient teaching and should not be left in the
manual while in the patient setting. Doing so could jeopardize
the security levels intended only for clinician use and access.
ese limits are designed to provide
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