Moog CURLIN INFUSION PainSmart, Руководство пользователя

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• The Bolus/Data Connector is to be used by the patient only for the connection of the bolus cord
with the remote switch. Other accessory equipment connected to this digital interface must
be certified to the respective IEC/EN standards (i.e. IEC 950 for data processing equipment
and EN 60601-1 for medical equipment). Furthermore, all configurations shall comply with
the system standard EN 60601-1. Anyone who connects additional equipment to the signal
input part or signal output part configures 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.
• The 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. These limits are designed to provide
reasonable protection against harmful interference in a typical medical installation.
• This 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 off 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 different from that to which the other
device(s) are connected.
4. Consult the manufacturer or field service technician for help.
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
Code” contains access code information, the entire chapter should be
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.
IMPORTANT
INFORMATION