Safety Designation Per Iec 60601-1 - CareFusion MicroLoop Manuel D'utilisation

Safety Designation per IEC 60601-1

Type of protection against
electrical shock
Degree of protection against
electrical shock
Power Equipment
Degree of Electrical connection
between equipment and Patient
Degree of mobility
Mode of operation
Classifications according to IEC 60601-1
MicroLoop
Volume Transducer
Option SPO2 Finger Probe
(Nonin IPOD® Integrated Oximetry Device)
WARNING: No modification of this equipment is allowed.
Note: When you connect other equipment to the unit, always make
sure that the whole combination complies with the international
safety standard IEC 60601-1 for medical electrical systems. During
measurements, connect the MicroLoop only to printers and
computers that comply with IEC/EN 60601-1 / UL 60601-1.
WARNING: The user must not touch any voltage-carrying parts and
the patient at the same time.
During database upload the Micro Loop may be connected to a
computer that that complies with EN 60950 – 'Information
technology equipment - Safety - Part 1: General requirements'.
Internally powered
Equipment and Class I
Type B applied part
Battery type: Lithium ion
polymer LP385085, 3.7V,
1600mAh
Equipment designed as
non-electrical connection to
the patient.
Transportable
Continuous
Applied part, type B
Applied part, type B
Applied part, type BF
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