enovis ARTROMOT K1 Mode D'emploi page 60

6.2 Maintenance
(fuse replacement)
Check before each use
Visually inspect the device for signs of me-
chanical damage before each use.
If you detect damage or malfunctions that
may impair the safety of the patient or
of the operator, have the device repaired
before using it.
Technical inspections
Due to their design, the bearings and
joints of the ARTROMOT®-K1 do not
require maintenance and all materials are
protected from corrosion, BUT: For safety,
the devices require regular maintenance.
To maintain the functional and operational
safety, check all components for damage
and loose connections at least once a year.
These checks should be performed by
persons with adequate training and experi-
ence. Damaged and worn parts must im-
mediately be replaced with original spare
parts by authorized staff.
Warning!
m
Patient hazard –
equipment malfunction and damage
− Refer repair and maintenance to
authorized persons. Persons are
authorized after training by a special-
ist trained and commissioned by the
manufacturer.
ORMED GmbH will make all docu-
ments required for servicing, such as
circuit diagrams, parts lists, descrip-
tions or calibration instructions, avail-
able to authorized experts.
The inspections can be carried out by DJO
Technical Service within the framework
of a service agreement. Contact DJO for
details.
Other than that, the manufacturer
does not require any other regular
maintenance.
Note!
Regarding further technical or other
inspections or inspection intervals,
observe applicable local requirements,
such as IEC 62353, DGUV3 or similar
regulations to be observed by users of
medical equipment or electric devices.
Fuse replacement
Warning!
m
Patient hazard –
equipment malfunction and damage
The replacement of fuses must be
referred to specialists as defined in DIN
VDE
0105 or IEC 60364 or other applicable
standards (e.g. biomedical technicians,
electricians, electronics installers).
Fuses used must be
S# < 20,000: T1A L250Vac
S# > 20,000: T2A H250Vac.
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