General Informations; Safety Notes; Definitions - Eurosets COLIBRI SYSTEM Instructions For Use Manual

1. GENERAL INFORMATIONS

1.1. SAFETY NOTES

Information to draw the user's attention to potentially dangerous situations and to ensure correct and safe use of
the device is indicated in the text as follows:
Warning
Indicates possibility of injury, death, or other serious adverse reaction associated with the use or
miuse of the device.
Caution
Indicates possibility of problem with the device associated with its use or misuse. Such problems
include device malfunction, device failure, damage to the device or damage to other property.

1.2. DEFINITIONS

COLIBRÌ SYSTEM:
Composed by COLIBRÌ Console, COLIBRÌ Flowmeter and COLIBRÌ Power Module.
COLIBRÌ FLOMETER:
Corresponds to:
- COLIBRÌ FLOWMETER 3/8" X 3/32" for Adult/Paediatric configuration.
- COLIBRÌ AIR/FLOW SENS 1/4" X 3/32" for New Born configuration.
COLIBRÌ CONSOLE:
Main electronic unit of COLIBRÌ System for operating, powering, controlling and regulating the operation of motor
driver.
CENTRIFUGAL PUMP:
Magnetic non-occlusive blood pump consisting in a rotating impeller arranged with vanes inside a plastic housing
with inlet and outlet ports. Blood is moved by centrifugal force with bearing-less magnetic levitation generated by
COLIBRÌ System.
HIGH PRIORITY ALARM:
Indicates that immediate intervention by the OPERATOR is required.
MEDIUM PRIORITY ALARM:
Indicates that timely intervention by the OPERATOR is required.
LOW PRIORITY ALARM:
Indicates that something requires the attention of the OPERATOR.
RESPONSIBLE ORGANIZATION:
The organization responsible for the use and the maintenance of the device. The RESPONSIBLE ORGANIZATION
can be, for example, a hospital or a medical practitioner.
APPLIED PART:
The part of the COLIBRÌ System which, under normal conditions of use, is in physical contact with the patient in
order to fulfil its function.
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