Operator's Manual
5
•
Never leave the pump unattended while on the clinician bolus edit screen. You must deliver the
programmed value, or cancel to leave the screen.
•
Do not prime the fluid path with the tubing connected to a patient as this could result in overdelivery
of medication or air embolism.
•
To prevent air embolism, ensure that the entire fluid path is free of all air bubbles before connecting to
the patient.
•
The remote dose cord is for patient use only. Operation by anyone other than the patient may cause
overdelivery of medication.
•
The manual program mode does not contain programming limits. Carefully review each parameter to
ensure it accurately matches the prescription.
•
Always carefully review the program on the pump after it has been programmed to verify that the
pump is programmed correctly.
• The pump and reusable accessories should be cleaned and disinfected after each patient use and
in accordance with this manual and your organization’s policies and procedures for reusable, solid
surface, non-critical medical devices.
•
Ensure that debris is not allowed to build up on the pressure plate surface of the pumping mechanism.
Inspect the air detector sensor slot and remove any debris. A blocked air detector sensor may not
detect air present in the fluid path.
•
Ensure that the ± 6% system delivery accuracy specification is taken into account when programming
the pump and/or filling the reservoir. Failure to do so may result in medication in the reservoir
becoming depleted sooner than expected.
•
System delivery inaccuracies beyond ± 6% may occur as a result of back pressure or fluid resistance,
which depends upon temperature, drug viscosity, catheter size, extension set tubing (for example,
microbore), in-line components (such as filters and needleless access connectors), and placing the
infusion reservoir and/or pump above or below the level of the patient. System delivery inaccuracy
may result in under or overdelivery of medication. (See System Delivery Accuracy on page 75 for more
information.)
•
The use of power supplies and a remote dose cord other than those listed in the electromagnetic
emissions declaration may result in increased emissions or decreased immunity of the pump.
•
Serious harm to the patient or operator may result from the use of modified parts or parts not
authorized by Smiths Medical. Do not modify the system, parts, or accessories.
•
The pump should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is
necessary, you should verify normal operation of the pump in the configuration in which it is to be used.
•
Common portable and mobile consumer electronic devices may cause interference with the pump.
Observe the pump to verify normal operation. If abnormal performance is observed, it may be
necessary to reorient or relocate the pump away from radio frequency transmitting devices.
•
To avoid electric shock, do not touch the Power Jack, Remote Dose Cord Jack, USB Port, Battery
Terminals, or any other connectors and the patient simultaneously.
•
Residential/facility wiring must comply with all applicable electrical codes. Do not bypass power cord
connections. Do not remove a prong from the power cord.
•
There are potential health hazards associated with improper disposal of batteries, electronics,
and contaminated (used) reservoirs and extension sets. Dispose of used batteries, reservoirs,
extension sets, and other used accessories, or a pump that has reached the end of its useful life, in an
environmentally safe manner, and according to any regulations that may apply.
•
Always set the Delivery Limit amount alarm, Reservoir Volume Low alarm, and all other variable alarm
settings to clinically appropriate settings. Setting alarm limits to values not clinically safe for the
patient may cause patient harm due to a delay in therapy.
•
To avoid any potential electrical interference or delivery inaccuracies, power off the pump when the
pump is being transported in an aircraft.