Smiths Medical CADD Solis 2100, Техническое руководство

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5
Introduction
• 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.
• 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.
• 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.
• 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.
Cautions
• Do not operate the pump at temperatures below 2°C (36°F) or above 40°C (104°F) to avoid damaging the
electronic circuitry.
• Do not store the pump at temperatures below –20°C (–4°F) or above 60°C (140°F) to avoid damaging
the electronic circuitry. Do not store the pump with a CADD™ medication cassette reservoir or CADD®
administration set attached.
• Do not expose the pump to humidity levels below 20% or above 90% relative humidity to avoid
damaging the electronic circuitry.
• Do not store the pump for prolonged periods with the batteries installed. Battery leakage could damage
the pump.
• Do not twist or turn the remote dose cord connector, or use any instrument to remove it from the pump.
• Inspect the AA batteries for damage or wear to the metal or plastic insulation prior to use, or after the
pump has been dropped or hit. Replace the batteries if any damage is noted.
• If the power up results in an error message indicating that the protocol library was lost, do not proceed
with using the pump. Follow your facility’s procedures for downloading protocol libraries.
• Do not immerse the pump in cleaning fluid or water. Do not allow solution to soak into the pump,
accumulate on the keypad, or enter the battery compartment, USB port, remote dose cord jack, or power
jack areas. Moisture buildup inside the pump may damage the pump.
• Do not oversaturate the chassis area on the bottom of the pump with cleaning or disinfecting solutions.
Oversaturating this area can cause damage to the pump sensors over time.
• Do not clean the pump with acetone, other plastic solvents, or abrasive cleaners, as damage to the pump
may occur. Also refer to the instructions for use for each accessory before proceeding with cleaning and
disinfecting. Some accessories may have their own list of acceptable cleaning and disinfecting solutions.
• CADD® pumps are sealed units. A broken or damaged seal will therefore be considered conclusive
evidence that the pump has been misused and/or altered, which voids any and all warranties. All service
and repair of CADD® pumps must be performed by Smiths Medical or its authorized agents.
• At the completion of the Downstream Occlusion Pressure Range Test 2, the pressure must be reduced
to zero before detaching the cassette from the pump; otherwise, the cassette may rupture. Safety glasses
should be worn while conducting or observing this test.