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© Cop
yrigh
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o R&D AB 2020. ALL RIGHT
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.
Check the product before each use. Check the following points with regard to wear and damage:
• Fabric
• Seams
Do not use damaged lifting accessories.
If anything is unclear, please contact the manufacturer or supplier.
Washing instructions
Please see the lifting accessorie’s product label and the attached appendix ”Care and Maintenance” of Liko Slings.
Periodic Inspection
The product must be inspected at least once every 6 months. More frequent inspections might be required if the product is used
or washed more often than normal. For protocols please contact your Hill-Rom representative.
Expected Life Time
The product has an expected life time of 3 years. The expected life time is based on 10 uses per day and washing once per week,
according to washing instructions. Hill-Rom recommends the product be used only during its expected life time.
Recycling Instructions
The Straps should be sorted as Combustible waste.
Hill-Rom evaluates and provides guidance to its users on the safe handling and disposal of its devices to aid in the prevention of injury,
including, but not limited to: cuts, punctures of the skin, abrasions, and any required cleaning and disinfection of the medical device
after use and prior to its disposal. Customers should adhere to all federal, state, regional, and/or local laws and regulations as it pertains
to the safe disposal of medical devices and accessories.
If in doubt, the user of the device shall first contact Hill-Rom Technical Support for guidance on safe disposal protocols.
Overview Liko
™
Straps Mod 600 IC, 8 pcs
Care and Maintenance
Liko AB
Nedre vägen 100
975 92 Luleå, Sweden
+46 (0)920 474700
www.hillrom.com
Liko AB is a subsidiary of Hill-Rom Holdings Inc.
Product Change
Liko’s 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 in Sweden
The management system for both manufacturing and development of the product is certified in accordance with ISO9001 and its
equivalent for the medical device industry, ISO13485. The management system is also certified in accordance with the environmental
standard ISO14001.
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.
Safety Instructions
Name
Prod. No.
Material
Length
Max. Load
Straps Mod 600 IC, 8 pcs
3684001
Polyester
140 cm (55 in)
250 kg (550 lbs)
