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Ipump Pain Management System Operator’s Manual
1-14
CD07-19-E4-766
CAUTION
As with all medical electronic equipment, exercise care to avoid exposing this pump to powerful
sources of electromagnetic interference. This device design has been tested to current U.S. and
European standards and guidelines for medical devices. The pump was not found to be affected
adversely by these susceptibility tests and will perform safely. The pump’s emissions also were
found to be acceptable. Using the pump near operating equipment that radiate high-energy radio
frequencies (such as electrosurgical/cauterizing equipment, two-way radios, or cellular tele-
phones) may cause false alarm conditions. If this happens, reposition the pump away from the
source of interference or turn off the pump.
CAUTION
Use only accessory equipment complying with the pump’s safety requirements; failure to do so
may lead to reduced safety levels of the resulting system. Consideration relating to accessory
choice shall also include the use of the accessory in the patient vicinity, and evidence that the
safety certification of the accessory has been performed in accordance with the appropriate
UL2601-1 (UL 60601-1) or IEC 60601-1 and/or IEC 60601-1-1 harmonized national standard.
CAUTION
Use this product for its intended use as described in this manual. Do not use attachments not
recommended by the manufacturer. If interconnection with other infusion systems and/or parallel
infusion is desired, make sure a recommended Anti-Reflux Y-Site Extension Set (2L3506) or a set
containing an integral Y-Site (2L3525, 2L3526, or 2L3527) is used to prevent back flow.
CAUTION
Follow the cleaning schedule and methods defined in “Preventive Maintenance,” 7-1, to ensure
the proper maintenance of the pump.
CAUTION
Any equipment connected to the pump through the PRINTER/COMM port must conform to the
electrical safety requirements of IEC 60601-1.
Oct02_0719E4766.book Page 14 Friday, August 3, 2007 1:46 PM