User`s manual

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The soft carry packs are intended for single patient use. They may be cleaned in the
gentle cycle of a washing machine using cold water, no chlorine bleach, and line dried.
(They cannot be dried in a clothes dryer.)
The 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 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 Curlin Medical representative.
The Curlin Medical 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
Introduction