Moog Curlin 6000 CMS IOD User Manual page 13

INFUSION PUMP
WITH RESPECT TO ELECTRIC SHOCK, FIRE
AND MECHANICAL HAZARDS ONLY
IN ACCORDANCE WITH UL60601-1/CAN/CSA C22.2 NO.
601.170TK
INTERNALLY POWERED OR FOR USE WITH AC ADAPTER 340 2022/360 2022KIT
AND 340 2026/360 2026 AND 47684 AND 47685
DEFIBRILLATION PROOF TYPE CF APPLIED PARTS
EQUIPMENT PROTECTED AGAINST DRIPPING WATER, IPX1
EQUIPMENT NOT SUITABLE FOR USE IN THE PRESENCE OF A FLAMMABLE
ANESTHETIC MIXTURE WITH AIR OR WITH OXYGEN OR NITROUS OXIDE
MODE OF OPERATION CONTINUOUS
•
In a life sustaining situation it is recommended that your Curlin Infusion pump use the AC
Adaptor and have a back-up pump available. Also provide an extra set of C-cell batteries in
addition to the batteries that are installed in the pumps.
•
User should be aware that the error in delivered drug volume may exceed ±5% when a syringe
is used with the Curlin infusion pump.
A mechanical problem, known as "stiction," may occur when the syringe is operated at low
plunger speeds. e friction between the syringe plunger and the barrel causes the plunger
to stick, then moves forward in a jerking motion, and the uid will be delivered as a series
of boluses. is e ect will cause variations larger than 5% in the delivered volume.
between the syringe plunger and the barrel may vary from batch to batch and, consequently,
the stiction e ect may also vary.
Due to this potential error, the delivery of powerful drugs with short half lives, such as
catecholamines is not recommended.
•
Use only Moog Curlin Infusion administration sets in your Moog Curlin Infusion pump.
Use of non-proprietary administration sets may alter accuracy in delivery of uids and could
result in over or under infusions, leading to possible patient injury or death.
•
Visually inspect the pump, pumping chamber and administration set before use. Do not use
any pump or administration set that appears to be damaged or tampered with or if there is any
indication of improper function.
WARNINGS
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