Inspection and Maintenance
For trouble-free operation, certain details should be checked each day the lift is used:
• Inspect the lift and check to make sure that there is no external damage.
• Check the sling bar attachment.
• Check the lift strap for wear and to ensure the strap is not twisted.
• Check the functionality of the latches.
• Check the operation of the lift movement.
• Check to make sure that the electrical emergency lowering functions correctly.
• Charge the batteries each day the lift is used and check to ensure that the charger works.
Clean the lift with a moist cloth. Find more detailed information regarding cleaning and disinfection of your
Liko
TM
product in
the chapter
“Cleaning and Disinfection”
.
The lift should not be exposed to running water.
Service
A periodic inspection of the lift should be carried out at least once per year.
Periodic inspection, repair and maintenance should be performed only in accordance with the Liko
TM
Service Manual
and by personnel authorized by Hill-Rom and using original Liko
TM
spare parts.
Service activities are not allowed with the patient in the lift.
Service Agreement
Hill-Rom offers the opportunity to enter into service contracts for the maintenance and periodic inspection of your
Liko
TM
products.
Expected Life Time
The product has an expected life time of 10 years when correctly handled, serviced and periodically inspected in accordance
with
Liko
TM
instructions.
Parts listed below are subject to wear and tear and have specific expected life time:
- Handcontrol, expected life time 2 years,
- Battery, expected life time 3 years.
- Liftstrap, expected life time 5 years.
Transport and Storage
During transportation, or when the lift is not to be used for a long time, the emergency stop should be engaged.
The environment where the lift is transported and stored should have a temperature of -10°C to +50°C (14°F to 122°F)
and a relative humidity of 20 to 90 %. The athmospheric pressure should be 700–1060 hPa.
Product Changes
Liko
TM
products undergo continuous development, which is why we reserve the right to make product changes without prior
notice. Contact your Hill-Rom representative for advice and information about product upgrades.
Design and Quality by Liko
TM
in Sweden
Liko is quality certified according to ISO 9001 and its equivalence for the medical device industry, ISO 13485.
Liko is also certified according to environmental standard ISO 14001.
Notice to Users and/or Patients in EU
Any serious incident that has occurred in relation to the device, should be reported to the manufacturer and the competent
authority of the Member State in which the user and/or patient is established.
Liko AB,
Nedre vägen 100
975 92 Luleå, Sweden
+46 (0)920 474700
Liko AB is a subsidiary of Hill-Rom Holdings inc.
www.hillrom.com
© Cop
yrigh
t Lik
o R&D AB 2019. ALL RIGHT
S RE
SER
VED
.
