Werbung
Verfügbare Sprachen
Verfügbare Sprachen
USER MANUAL FOR
● Disassembly, cleaning and lubrication of front and rear castors.
● Disassembly, cleaning and lubrication of the mast hinge.
● Check the fastening, wheel play, and efficiency of the brakes.
● Check the welds. Visual inspection.
● Check the alignments. Visual inspection.
● Check and lubricate after dismantling the mast and hanger bar
pivots.
● Check and grease the actuator fasteners.
● Re-tighten all parts.
Mechanical parts showing cracks, signs of wear or geometric
defects must be replaced with original components supplied by
Drive DeVilbiss Healthcare France.
VIII-5.2) ELECTRICAL INSPECTION
● Check the handset.
● Check the charger.
● Check the remote control box and the actuator.
● Check the lifting/lowering speed.
● Check the emergency stop and lowering.
● Condition of the electric cables (change the cables if in doubt).
Replace the electric cables, and/or the components to which they
are connected, if they show signs of wear, sheathing cuts, plug
degradation or blackening of the plastics and sheathing around
the connection areas. Replace defective components with original
ones. Never disassemble the protective covers of the actuator,
battery pack, handset, control box and battery charger.
VIII-5.3) CHARGING TEST
● Charge the battery pack.
● Check the power and autonomy of the battery pack.
● Test of the patient when fully loaded at 175 Kg and check the
cut threshold (230 Kg ± 10 Kg).
VIII-5.4) MAINTENANCE MANUAL
Every maintenance operation or intervention must be recorded in
the maintenance manual attached to these instructions.
VIII-5.5) LIST OF SPARE PARTS
A list of spare parts is available on request.
IX - SHIPPING, STORAGE, AND
DISPOSAL
● The patient lift must be returned or transported in its original
packaging.
● Before storing the patient lift, clean it thoroughly and check its
operation; store it in a dry room away from dust and moisture.
The batteries must be fully charged every 3 months.
● When commissioning after storage, charge the battery pack,
and check the operation before further use.
● Storage temperature: ....................................................0 to +50°C
....................................................... Humidity between 10 and 80%
● Operating temperature: ............................................ +10 to +40°C
...................................................... Humidity between 30 and 80%
30
SAMSOFT 175
● Defective parts, packaging, and battery packs must be
disposed of at authorised waste treatment centres.
● The device in question must not be disposed of with
household waste, and must be handed in to an appropriate
waste collection point or a distributor. The patient lift is subject
to Directive 2002/96/EC on waste electrical and electronic
equipment (WEEE) and marketed after 13 August 2015.
● By following these guidelines, you are doing your bit for the
environment by helping to preserve natural resources and
protect human health.
X - WARRANTY CONDITIONS AND
LIABILITY
The SAMSOFT 175 is guaranteed for 5 years on structure, cylinder,
and control box, in normal use according to the instructions given in
this manual. Negligence, handling errors or accidents are excluded
from the warranty. The remote control is guaranteed for 3 months,
and the battery pack is guaranteed for 6 months.
● Any modification or addition of accessories without written
consent from Drive DeVilbiss Healthcare France, will de facto
exclude the patient lift from the warranty and from Drive
DeVilbiss Healthcare France's liability. In particular, we cannot
be held liable for the use of slings not marketed by Drive
DeVilbiss Healthcare France for this patient lift.
● The periodic checks and inspections mentioned in the
previous paragraph must be carried out by competent
personnel and recorded in the maintenance book. Out of
the warranty period, we cannot be held responsible if these
checks and inspections are not carried out. Only spare parts
and components supplied by Drive DeVilbiss Healthcare
France can be used for repairs.
● Any serious incident occurring in connection with this patient
lift must be notified to the manufacturer and to the competent
authority of the Member State in which the user and/or patient
is established.
EN
Werbung
