User guide

12
MAN 01/EN/03 CRONO PAR 50 06/13
The device must be used:
- under medical supervision,
- with appropriate procedures and adequate measures when dealing with
patients who could suffer serious consequences (injury or death) in the event
of accidents and/or breakdowns which cause an interruption of the admini-
stration of the drug.
Do not prime the infusion line when it is connected to the patient, because
this could cause an overdose of the drug.
Before beginning an infusion, inspect the infusion line to ensure there are no
folds, clamps or other occlusions in the line, and expel any air bubbles.
The level of precision and the amount of time needed to detect an occlusion
could differ from the values indicated in this User Guide for the elements
composing the infusion line.
If you have any suspicion that the pump has been in any way damaged, for
example by liquid penetration or having been dropped, contact the Customer
Support Service to check that the pump is functioning correctly. Do not use a
damaged pump.
If you have any doubts about the functioning of the pump and/or an error or
anomaly occurs, stop using the device and contact the Customer Support
Service.
CANĂˆ S.p.A. does not supply a replacement service for the pump during
the period needed for any repairs; such a service should be supplied by the
relevant medical structure or the local distributor.
Any liquid on the pump casing must be removed immediately with paper
towels.
It is important to establish a procedure and/or alternative to pumped infusion,
in case the pump malfunctions. Possible solutions could either be to have a
secondary pump or to have an alternative system.
It is recommended that the individuals who assist and/or live with the pump
user know how the pump works and the information in this User Guide.
It is important to stop using the device after the indicated service life has ex-
pired and follow the instructions for its correct disposal.
SECTION 3










