Product Descripon

In this document, the person being lied is referred to as the paent, and the person helping them is referred to as the

caregiver.

Likorall overhead li is a staonary li unit oen called an

“overhead li”. Likorall overhead li is mounted in LikoTM

rail system, which is adapted to suit the room/rooms it

will be operated in. The rail system can be built straight,

with or without curves, as a traverse system and also as a

room-to-room system. LikoTM rail system is comprised of

Likorall overhead li is intended for use in liing and transferring

paents, for example, from bed to a wheelchair, to or from

the oor, for visits to the toilet, for gait, standing and balance

training, when weighing the paent and when liing the

paent with a stretcher.

Likorall 200 overhead li is adapted to the LikoTM Quick-release

Hook System for safe and easy changing of liing accessories.

The LikoTM Room-to-Room system (R2R), enables the paent

to be moved between two rail systems in separate rooms,

without connecng rails and without making holes over doors.

7EN120114 Rev. 10

ENGLISH 2020

IMPORTANT!

Liing and transferring a paent always involves a certain level of risk. Read the instrucons for use for both the paent

li and liing accessories before use. It is important to completely understand the contents of the instrucons for use.

The equipment should only be used by trained personnel. Ensure that the liing accessories are suitable for the li used.

Exercise care and cauon during use. As a caregiver, you are always responsible for the paent’s safety. You must be aware of

the paent’s ability to make it through the liing situaon. If something is unclear, contact the manufacturer or supplier.

EMC Table ......................................................................................................................................... 6

Assembly .......................................................................................................................................... 9

Operaon ......................................................................................................................................... 9

Charging the Baeries .................................................................................................................. 12

Transferring from Room to Room ................................................................................................... 13

Maximum Load ............................................................................................................................... 14

Recommended Liing Accessories ................................................................................................. 14

Simple Troubleshoong .................................................................................................................. 16

Recycling Instrucons ..................................................................................................................... 17

Cleaning and Disinfecon .............................................................................................................. 18

Symbol Descripon

Safety Instrucons

• the sling bar latches are intact; missing or damaged latches must always be replaced

• the sling strap loops are correctly connected to the sling bar hooks when the sling´s strap is extended upward, but before

the paent is lied from the underlying surface.

Electromagnec disturbance, may aect the liing performance of the product. Modicaon using other parts than original

spare parts (cables etc.) may aect the electromagnec compability of the product.

Parcular care must be observed when using strong sources of electromagnec disturbance, such as diathermy, etc, so that dia-

thermy cables are not posioned on or near the li. If you have quesons, please consult the responsible assisve-device technician

paent shall always be performed with the assistance of at least one caregiver. This product is used as a means to perform the li

but is not in contact with the

your Hill-Rom representave for support and advice.

Likorall 200 is tested by an accredited tesng instute.

Valve-regulated lead-acid gel-

type baeries. New baeries are

provided by the supplier.

Immunity test IEC 60601 test level Compliance level Electromagnec environment - guidance

Electrostac discharge

(ESD)

IEC 61000-4-2

Electrical fast transient

/ Burst

IEC 61000-4-4

voltage variaons on

power supply input

IEC 61000-4-11

IEC 61000-4-6

Radiated RF

IEC 61000-4-3

NOTE UT is the a.c. mains voltage prior to applicaon of the test level.

The product is intended for use in the electromagnec environment specied below. The customer or the user of this

product should assure that it is used in such an environment.

level

Electromagnec environment - guidance

Portable and mobile RF communicaons equipment should

Radiated RF

IEC 61000-4-3

10 V/m

80MHz to 2,5GHz

80 MHz to 800 MHz

800 MHz to 2,5 GHz

where P is the maximum output power rang of the transmier

the following symbol.

NOTE 1 At 80MHz and 800MHz, the higher frequency range applies.

NOTE 2 These guidelines may not apply in all situaons. Electromagnec propagaon is aected by absorpon and reected

from structures, objects and people.

amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theorecally with accuracy. To assess the

electromagnec environment due to xed RF transmiers, an electromagnec site survey should be considered. If the mea-

sured eld strength in the locaon in which the product is used exceeds the applicable RF compliance level above, the product

should be observed to verify normal operaon. If abnormal performance is observed, addional measures may be necessary,

such as reorienng or relocang the product.

• the li’s funcons correspond to the markings of the

hand control

• the electrical emergency lowering device

funcons properly

Push down the red catch and connect the quick-release hook to the Q-Link II or Q-Link. Release

and check that the catch locks in order to prevent involuntary unhooking from the Q-Link II

or Q-Link. Read more about the Liko

The liing moon in LikorallTM 200 overhead li is controlled

using an aached hand control. LikorallTM 200 overhead li

is manoeuvered by pressing lightly on the hand control

buons. The arrows indicate direcon. Moon ceases when

the buon is released.

device to lower the paent onto a rm surface.

4. Charge the baery.

5. If the problem persists, please contact Hill-Rom.

Please contact Hill-Rom.

regional, and/or local laws and regulaons as it pertains to the safe disposal of medical devices and accessories.

If in doubt, the user of the device shall rst contact Hill-Rom Technical Support for guidance on safe disposal protocols.

These instrucons do not replace the facility’s own cleaning and disinfecon policies.

To help prevent injury and/or equipment damage, obey these warnings:

• Warning—The potenal for electrical shock exists with electrical equipment. Failure to follow facility protocol could cause

death or serious injury.

• Warning—Do not reuse wiping material for mulple steps or on mulple products.

• Warning—Harmful cleaning soluons may cause skin rash and/or irritaon upon contact.

• Cauon—Do not steam clean or power wash the li. Pressure and excessive moisture can damage

the protecve surfaces of the li and its electrical components.

• Cauon—Do not use harsh cleansers/detergents, heavy duty grease removers, solvents such as toluene,

xylene, or acetone, and do not use scouring pads (you may use a so bristle brush).

• Cauon—Fully extend the li strap prior to the cleaning and disinfecon process.

• Wear protecve equipment according to manufacturer’s instrucon and per facility protocol

throughout the cleaning operaons, such as: gloves, eye protecon, apron, face mask and shoe covers.

• Unplug mains (AC power source) before cleaning and disinfecon.

• Never clean the li by pouring water on it, steam cleaning it, or by using a high-pressure jet.

• Clean and disinfect the product while the trainer supervises. During, and/or aer this process,

the trainer should correct the trainee about any dierences from the instrucons for use.

The trainer should supervise the trainee unl the trainee can clean and disinfect the li as instructed.

Hill-Rom recommends to clean and disinfect the li between paent use and regularly during extended paent stays.

Some uids used in the hospital environment, such as iodophor and zinc oxide creams, can cause

permanent stains. Remove temporary stains by wiping vigorously with a lightly-dampened wiping