Likorall 242/243/250 Overhead Lifts
Instructions for Use
Product Models:
- Likorall 242 S lift (Prod. no. 3122009-3122010)
- Likorall 242 ES lift (Prod. no. 3122005-3122006)
- Likorall 242 S R2R lift (Prod. no. 3122011-3122012)
- Likorall 242 ES R2R lift (Prod. no. 3122007-3122008)
- Likorall 243 ES lift (Prod. no. 3123001-3123002)
- Likorall 250 ES lift (Prod. no. 3122501-3122502)
- Likorall 250 S, IRC lift (Prod. no. 3124050)
Product Description
The Likorall overhead lift is a general-purpose lifting device designed for use in healthcare settings, including general care, intensive care, and rehabilitation. It integrates seamlessly with Liko's fixed and free-standing rail systems, offering ease of use and accessibility. The lift facilitates common patient transfers, such as between bed/wheelchair, to/from the floor, for toilet visits, gait training, and with stretchers. The Likorall R2R model allows for patient movement between two separate rail systems in different rooms without requiring wall modifications.
The Likorall ES models are equipped for wireless operation via the HandControl Remote (IR) and can also accommodate a Transfer Motor for powered rail movement. The Likorall S, IRC model features continuous charging through the rail system via the Liko In-Rail charging system (IRC).
A wide range of accessories, including various sling models in different sizes and designs, are available for the Likorall overhead lift.
Intended Use
This product is designed for use by trained personnel assisting a patient. It is not intended for patient self-operation. Lifting and transferring a patient must always be performed with the assistance of at least one caregiver. This manual focuses on the operation of the lift itself, not specific patient conditions. For support and advice, contact a Hillrom representative.
IMPORTANT! Lifting and transferring patients involves inherent risks. Always read and understand the instructions for use for both the lift and lifting accessories before operation. Ensure lifting accessories are compatible with the lift. Exercise care and caution; the caregiver is responsible for patient safety and must assess the patient's ability to manage the lifting situation. Contact the manufacturer or supplier if anything is unclear.
Symbol Description
The following symbols are used in this document and on the product:
- Indoor Use Only: Symbol indicating the product is for indoor use.
- Insulation Class II: Symbol indicating extra protection against electric shock.
- Type B Protection: Symbol indicating protection level against electric shock.
- Warning: Symbol indicating extra care and attention are needed.
- Read Instructions: Symbol indicating to read instructions before use.
- CE Mark: European Union medical device conformity mark (Class I Medical Device).
- IP Rating (N1, N2): Protection level against ingress of solid objects (N1) and water (N2).
- Manufacturer: Symbol indicating the manufacturer.
- Date of Manufacture: Symbol indicating the date of manufacture.
- Caution: Symbol indicating to consult instructions for use.
- Battery: Symbol indicating batteries are present.
- Recycling Symbols: Indicate batteries and EEE must be recycled separately.
- UL Recognized Component Mark: For Canada and the United States.
- EFUP: Environmental Friendly Usage Period (years).
- Recyclable Symbol: Indicates the product is environmentally friendly and can be recycled.
- Australian Safety/EMC: Symbol for Australian Safety and EMC compliance.
- PSE Mark (Japan): Symbol for Japan's product safety conformity.
- REF: Product Identifier.
- SN: Serial Number.
- MD: Medical Device.
- Recyclable: General recyclability symbol.
- EMC Verified: Indicates compliance with electromagnetic compatibility standards.
- Non-ionizing electromagnetic radiation: Symbol indicating non-ionizing radiation.
Technical Data
Parameter | Details |
---|---|
Maximum Load | Likorall 242 lift: 200 kg (440 lbs) Likorall 243 lift: 230 kg (507 lbs) Likorall 250 lift: 250 kg (550 lbs) |
Batteries | 2 x 12 V (2.4 Ah - 2.6 Ah) Valve-regulated lead-acid gel-type batteries. |
Battery Charger | CH01 FW7218M/24 (100-240 V AC, 50-60 Hz, max 500 mA) SMP CC-10-43-24 (100-240 V AC, 40-60 Hz, max 600 mA) IRC: CH01 FW7218M/24 (100-240 V AC, 50-60 Hz, max 500 mA) |
Lifting Speed | 50 mm/s (2 inch./s) |
Lifting Interval | 2050 mm (80.7 inch.) (242 vertically adjustable) |
Electrical Data | 24 V, 12 A |
Lift Motor Weight | Likorall 242 lift: 13.0 kg (28.6 lbs) Likorall 242 R2R lift: 12.6 kg (27.7 lbs) Likorall 243 lift: 12.6 kg (27.7 lbs) Likorall 250 lift: 12.6 kg (27.7 lbs) |
Emergency Lowering Device | Mechanical: Likorall 242 S/ES Electrical: Likorall 242 R2R lift, Likorall 243 lift, Likorall 250 lift |
Intermittent Operation | Int. Op 10/90, active operation max 30 Sec. |
Sound Level | 49 dB |
Protection Class | IP 43 (hand control: IP 54 for Prod. No. 3126050; IP 43 for Prod. No. 3126035, 3126036, 3126038, 3126060) |
Operating Forces of Controls | 3 N (for Prod. No. 3126050); 5 N (for Prod. No. 3126035, 3126036, 3126038, 3126060) |
Ambient Temperature | Min. +10°C - Max. +50°C (Min. 50° F - Max. 122° F) |
Intended Use | Indoor use only. |
Electrical Shock Protection | Type B, in accordance with the electrical shock protection class. |
The Likorall overhead lift features a patented SFS (Single Fault Safety) safety drum, providing protection against uncontrolled lowering. The lift strap has a tenfold safety mechanism.
Measurements
Diagram Description: The diagram illustrates lateral and overhead views of the Likorall lift system, showing key measurement points (A, B, C, D, H, L) relative to the ceiling, suspension point (CSP), and carriage.
Dimension | Measurements in mm | Measurements in inch | |||||
---|---|---|---|---|---|---|---|
A | B | C | D* | H** | L*** | ||
Likorall 242/243/250 | 165 | 340 | 250 | 304 | - | - | |
Likorall 242 R2R, 243, 250 | - | - | - | 221 | - | - | |
Likorall 242 | - | - | - | 346 | - | - | |
Likorall 242 | - | - | - | - | 8.7 | 13.6 | |
Likorall 242 R2R, 243, 250 | 6.5 | 13.4 | 9.8 | 12.0 | - | - | |
Likorall 242 | - | - | - | - | - | 80.7 |
* Minimum distance from ceiling to CSP at maximum lifting height with standard carriage.
* Built-in dimension: distance between attachment point and CSP at maximum lifting height.
* Lifting interval: distance between maximum and minimum lifting height measured in CSP.
EMC Table and Guidance
This section provides guidance and declarations regarding electromagnetic compatibility (emissions and immunity) for the Likorall overhead lift, in conjunction with specific accessories like the Hand control (3126050) and battery chargers (3126131-134, 3126135). The configurations comply with IEC 60601-1-2 standards.
Electromagnetic Emissions Guidance
Emissions Test | Compliance | Electromagnetic Environment - Guidance |
---|---|---|
RF emissions CISPR 11 | Group 1 | The product uses RF energy internally. Emissions are low and unlikely to interfere with nearby electronic equipment. |
RF emissions CISPR 11 | Class B | - |
Harmonic emissions IEC 61000-3-2 | Class A (with 3126135 charger) / Complies (with 3126131-134 charger) | Suitable for domestic and public low-voltage power supply networks. |
Voltage fluctuations/flicker emissions IEC 61000-3-3 | Complies | - |
Electromagnetic Immunity Guidance
Immunity Test | IEC 60601 Test Level | Compliance Level | Electromagnetic Environment - Guidance |
---|---|---|---|
Electrostatic discharge (ESD) IEC 61000-4-2 | +/- 8 kV contact, +/- 15 kV air | +/- 8 kV contact, +/- 2, 4, 8, 15 kV air | +/- 8 kV contact, +/- 15 kV air (relative humidity >= 15%). |
Electrical fast transient/Burst IEC 61000-4-4 | +/- 2 kV for power supply lines, +/- 1 kV for input/output lines | +/- 2 kV for power supply lines, n/a for input/output lines | Mains power quality should be typical of commercial, hospital, or home healthcare environments. |
Surge IEC 61000-4-5 | +/- 1 kV differential mode, +/- 2 kV common mode | +/- 0.5 & 1 kV differential mode, n/a for common mode | Mains power quality should be typical of commercial, hospital, or home healthcare environments. |
Voltage dips, short interruptions, voltage variations IEC 61000-4-11 | 0% UT for 0.5 cycle, 40% UT for 5 cycles, 70% UT for 25 cycles, <5% UT for 250 cycles (50Hz) / 300 cycles (60Hz) | 0% UT for 0.5 cycle, 40% UT for 5 cycles, 70% UT for 25 cycles, <5% UT for 250 cycles (50Hz) / 300 cycles (60Hz) | Mains power quality should be typical of commercial, hospital, or home healthcare environments. For continued operation during interruptions, use an uninterrupted power supply or battery. |
Power frequency (50/60 Hz) magnetic field IEC 61000-4-8 | 30 A/m | 30 A/m | Power frequency magnetic fields should be at levels characteristic of typical commercial, hospital, or home healthcare environments. |
Proximity Magnetic Fields | 8 A/m (CW mod. 30kHz), 65 A/m (2.1kHz pulse mod. 134.2kHz), 7.5 A/m (50kHz pulse mod. 13.56MHz) | 8 A/m (CW mod. 30kHz), 65 A/m (2.1kHz pulse mod. 134.2kHz), 7.5 A/m (50kHz pulse mod. 13.56MHz) | Proximity magnetic fields should be at levels characteristic of typical commercial or hospital environments. |
Recommended Separation Distances for RF Communications Equipment
This product is intended for use in environments where RF disturbances are controlled. Maintain minimum distances between portable/mobile RF equipment and the product based on the transmitter's maximum output power (P) and frequency, using the formulas provided (d = (0.58)√P for 150 kHz-80 MHz, d = (0.35)√P for 80 MHz-800 MHz, d = (0.70)√P for 800 MHz-2.7 GHz). Field strengths from fixed transmitters should be less than compliance levels. Interference may occur near equipment marked with the symbol for electromagnetic fields ((())).
Rated Maximum Output Power of Transmitter (W) | Separation Distance According to Frequency of Transmitter (m) | ||
---|---|---|---|
150 kHz to 80 MHz | 80 MHz to 800 MHz | 800 MHz to 2.7 GHz | |
0.01 | d = (0.58)√P = 0.06 | d = (0.35)√P = 0.04 | d = (0.70)√P = 0.07 |
0.1 | 0.18 | 0.11 | 0.22 |
1 | 0.58 | 0.35 | 0.70 |
10 | 1.84 | 1.11 | 2.21 |
100 | 5.83 | 3.50 | 7.00 |
Note: For transmitters not listed, estimate separation distance using the formula. At 80 MHz and 800 MHz, use the higher frequency range. Guidelines may vary based on site-specific propagation.
Operation
The Likorall overhead lift is operated using a hand control with buttons corresponding to lifting/lowering and movement direction. The lift stops when a button is released. For Likorall ES models, wireless IR hand controls are available.
Button Functions:
- Up/Down Arrow: Lifting movement (Up/Down).
- Movement Direction Arrow: Transfer motor control.
- Control Switch System: Indicates the control system type.
Hand Control Operation:
- Press buttons lightly; arrow directions match illustration.
- Movement ceases upon button release.
- For Likorall ES, multiple hand controls are available, including IR for wireless use.
- Lifting motion can also be controlled via buttons on the lift's end cover if the hand control is unavailable.
Emergency Stop:
- Pull the red emergency stop cord to stop the lift.
- Reset by turning the button in the direction of the arrows.
- The red cord is located on the lift motor's end cover.
Activate/Reset:
- Activate: [Diagram showing activation mechanism]
- Reset: [Diagram showing reset mechanism]
Q-Link or Q-Link II with Quick-Release Hook:
- Used for lifting accessories (e.g., Likorall 242 R2R, 243 ES, 250 ES).
- To attach, push down the catch and connect the hook to the Q-Link II or Q-Link.
- Release and verify the catch locks to prevent involuntary unhooking.
- Safety Check: Before lifting, ensure the Quick-release Hook is correctly attached to the Q-Link II or Q-Link.
Correct Lifting Procedure:
- Ensure sling loops are at the same height on both sides.
- Verify all sling loops are securely fastened to the slingbar hooks.
- Confirm the slingbar is level during the lift (See Figure 1).
- If the slingbar is not level (Figure 2) or sling loops are wrongly attached (Figure 3), lower the user to a firm surface and adjust. Improper lifting can cause discomfort or equipment damage.
Mechanical Emergency Lowering (Likorall 242 S/ES):
- Move the emergency lowering handle up and down until the patient is lowered and the lift strap is slack. Ensure lowering occurs onto a bed, wheelchair, or suitable surface.
- After lowering, reset/adjust lifting height: Lower the sling bar to slacken the strap, hold the handle halfway, and simultaneously tighten the strap by turning the black wheel counter-clockwise. Repeat until desired height is achieved.
Electrical Emergency Lowering:
- Push the button on the lift's end cover.
- Always ensure emergency lowering is to a bed, wheelchair, or suitable location.
Carriages with Adjustable Friction Brake:
- Drag along the rail can be adjusted by turning the friction brake clockwise (increase resistance) or counter-clockwise (reduce resistance).
- Carriages with friction brake include prod. no. 3126011 and 3126015.
Hang-up HandControl Hanger:
- Use to store the hand control when not in use.
SSP Limit Switch:
- Stops lifting motion electrically if the strap, Q-Link, or Q-Link II touches the switch, or if the strap is strained (e.g., pulled sideways, folded).
- After activation, the lift can be operated again once the strap is straight. A short delay is normal.
- Protects the lift motor from strain and prevents squeeze injuries.
- Ensure the lift strap remains straight and stretched during operation.
Charging Indications:
- Buzzer: Sounds when lifting, indicating low battery.
- LED (Red): Flashes when lifting, indicating low battery.
- When these signals occur, charge the lift as soon as possible.
Important Operation Note: Never move the lift by pulling the hand control!
Installation of Latches:
- After installation, check that latches lock and move freely in the sling bar hook.
Charging the Batteries
Regular charging is recommended for maximum battery life. Charge after use or nightly. Full charge takes up to 8 hours and provides approximately 60 lift cycles.
Note: If the lift is unused for an extended period, activate the charging system or press the emergency stop button to prevent battery discharge.
Never activate more than one charging system simultaneously.
Charging via Hand Control (Prod. No. 3126034-3126036, 3126038 charging station Prod. No. 3126101-3126104, 3126107)
- Ensure the emergency stop button is not pressed during charging.
- Place the hand control in the charger's socket.
- Connect the charger to a 100-240 V AC mains connection.
- Green LED (charger): Indicates connection to wall power.
- Yellow LED (charger): Illuminates when charging starts and turns off when fully charged.
Charging via Hand Control (Prod. No. 3126050, charging station Prod. No. 3126131-3126135)
- Ensure the emergency stop button is not pressed during charging.
- Place the hand control in the charging station and connect the charger.
- Connect the charger to a 100-240 V AC mains connection.
- LED (hand control): Illuminates to indicate connection to wall power.
- Orange LED (charger): Illuminates when charging starts; turns green when fully charged.
Alternative Charging Procedures
- In-Rail Charging (IRC): The lift charges continuously when on the rail. Charging pauses during lifting and resumes automatically. A green LED indicates readiness; a yellow LED indicates low battery capacity.
- MultiStation: Batteries can be charged by parking the lift under a MultiStation installed on the rail system. This requires the lift to be equipped with a contact rail or transfer motor. Suitable for HandControl IR operation as well. (Prod. No. 3126110)
Transferring from Room to Room
The Liko R2R Room-to-Room system facilitates safe patient transfers between rooms using separate rail systems. It links two Likorall overhead lifts for a comfortable transition.
Diagram Description: The diagram shows two lifts (Lift 1 and Lift 2) and the R2R system components (R2R double hook, Q-Link II/Q-Link, catches). It illustrates the steps for transferring a patient from Lift 1 to Lift 2.
Mounting a Q-Link to the Sling Bar R2R:
- A sling bar R2R with a double hook accommodates two Q-Links (II or standard).
- Catches secure the Q-Link II in the R2R double hook before load is applied.
- Open the catch gently to insert or remove a Q-Link II or Q-Link.
Transfer Steps:
- Move Lift 1 close to the doorway, lowering the lift as much as comfortable for the patient.
- Move Lift 2 close to the opening, lower its strap, and connect the Q-Link II or Q-Link to the sling bar R2R. Ensure R2R double hook catches function correctly.
- Raise Lift 2 to move the patient to the next room. Once pressure is relieved from Lift 1's strap, disconnect it from the sling bar R2R.
Note: For multi-room transfers, an adjustable carriage may be used instead of a lift motor. To detach Q-Link II/Q-Link, additional strap may need to be released from Lift 1.
Extend the Lift Strap with Extension Belt
Extension Belts are available in four adjustable lengths (300-500 mm, 500-700 mm, 750-950 mm, 1000-1200 mm) to extend the lift strap. Select the appropriate length for required extension, ensuring correct attachment and detachment of sling loops.
Diagram Description: The diagram shows how to attach a Quick-release Hook on an Extension Belt to the Q-Link II on the lift unit's lift strap.
- Safety Check: Before lifting, confirm the Quick-release Hook is correctly attached to the Q-Link II.
- When an Extension Belt is attached, the Central Suspension Point (CSP) is defined as the Q-Link II on the Extension Belt.
Maximum Load
The maximum load for an assembled lift system (lift, sling bar, sling, accessories) is the lowest maximum load rating of any component. For example, if the lift is rated for 200 kg and an accessory for 300 kg, the system's maximum load is 200 kg.
Consult markings on the lift and accessories, or contact Hillrom for clarification.
Recommended Lifting Accessories
Using unapproved accessories poses a risk. The following are generally recommended sling bars and accessories for the Likorall overhead lift. Some may not be currently available.
- Universal SlingBar 350 with Quick-release Hook (Prod. No. 3156084, Fixed connection: 3156074*, Max. load 300 kg)
- Universal SlingBar 450 with Quick-release Hook (Prod. No. 3156085, Fixed connection: 3156075*, Max. load 300 kg)
- Universal SlingBar 600 with Quick-release Hook (Prod. No. 3156086, Fixed connection: 3156076*, Max. load 300 kg)
- Universal SlingBar 670 Twin with Quick-release Hook (Prod. No. 3156087, Fixed connection: 3156077*, Max. load 300 kg)
- Universal SideBars 450 including bag (Prod. No. 3156079, Max. load 300 kg)
- Sling Cross-bar 450 with Quick-release Hook (Prod. No. 3156022, Fixed connection: 3156021*, Max. load 300 kg)
- Sling Cross-bar 670 with Quick-release Hook (Prod. No. 3156019, Fixed connection: 3156018*, Max. load 300 kg)
- Universal SlingBar 350 R2R (Prod. No. 3156094, Max. load 300 kg)
- Universal SlingBar 450 R2R (Prod. No. 3156095, Max. load 300 kg)
- Carriage Adapter Likorall for S65 (Prod. no. 3126030)
* Sling bars with fixed connection can be equipped with Quick-release Hook.
Extension Belts, adjustable:
- 300-500 mm (12-20 in) (Prod. No. 3121670)
- 500-700 mm (20-27 in) (Prod. No. 3121671)
- 750-950 mm (30-37 in) (Prod. No. 3121672)
- 1000-1200 mm (40-47 in) (Prod. No. 3121673)
Carriage Adjustable (R2R):
- 300-500 mm (12-20 in) (Prod. No. 3121660)
- 500-900 mm (20-35 in) (Prod. No. 3121661)
- 900-1300 mm (35-51 in) (Prod. No. 3121662)
Quick-release Hooks:
- Universal (Prod. No. 3156508)
- TDM (Prod. No. 3156502)
Stretchers: All Liko stretchers are compatible with Likorall lifts.
- Liko FlexoStretch (Prod. No. 3156057)
- Liko OctoStretch with Leveler (Prod. No. 3156056)
- Liko Stretch Mod 600 IC, wide (Prod. No. 3156065B)
- Liko UltraStretch (Prod. No. 3156058)
Other Accessories:
- SlingBar Cover Paddy 30
- Hang-up HandControl Hanger (set of 10 pcs.)
- Multi-Connector
- Transfer motor Likorall ES Overhead Lift (Max. 250 kg)
- HandControl LR S, ES, 2 buttons
- HandControl LR ES-4MS
- HandControl LR ES-4MT
- HandControl LR ES-6MT
- HandControl Remote IR
- Parking Panel 600, LR/MR
- Parking Panel 1500, LR/MR
- Hook for SlingBar
- Hook for Accessories
- Bracket for Charger
Optional Components for Use with Lift:
- LikoScale Device (for weighing patients): LikoScale 350 (Max 400 kg, Prod. No. 3156228 / 3156228FR for France), LikoScale 200 (Max 200 kg, Prod. No. 3156225), LikoScale 400 (Max 400 kg, Prod. No. 3156226).
Troubleshooting
- Lift doesn't work: Check emergency stop, hand control connection, and battery charge. Contact Hillrom if issues persist.
- Repeated signal: Charge the battery immediately. Contact Hillrom if issues persist.
- Lift stuck in high position: Check emergency stop, hand control connection, use emergency lowering to a safe surface, and charge the battery. Contact Hillrom if issues persist.
- Lift not achieving maximum capacity: Charge the battery. Contact Hillrom if issues persist.
- Unusual sounds or leakage: Contact your Hillrom representative.
Recycling Instructions
Dispose of old batteries at designated recycling stations or authorized personnel. The Likorall overhead lift complies with the EU Directive 2012/19/EEC on waste electrical and electronic equipment.
Hillrom provides guidance on safe handling and disposal of devices. Adhere to all applicable federal, state, regional, and local laws and regulations for medical device disposal. Contact Hillrom Technical Support for guidance if unsure.
Diagram Description: The diagram illustrates the separation of components for recycling: Pb-batteries, Metals, and Waste of Electrical and Electronic Equipment (WEEE).
Cleaning and Disinfection
These instructions supplement facility cleaning policies.
Warnings:
- Electrical shock hazard exists; follow facility protocols.
- Do not reuse wiping material across multiple steps or products.
- Harmful cleaning solutions may cause skin irritation; follow product label and SDS instructions.
- Lift and move items correctly; seek assistance if needed.
- Fluid spills on electronics can create a hazard; ensure the lift is completely dry and tested before reuse.
Cautions:
- Do not steam clean or power wash; pressure and moisture can damage surfaces and electronics.
- Avoid harsh cleansers, solvents (toluene, xylene, acetone), and scouring pads (soft bristle brush is acceptable).
- Fully extend the lift strap before cleaning and disinfection.
Safety Recommendations:
- Wear appropriate Personal Protective Equipment (PPE) during cleaning.
- Unplug the mains (AC power) before cleaning.
- Never pour water on the lift, steam clean, or use a high-pressure jet.
- Follow recommendations from the cleaning product manufacturer.
Process Recommendations:
- Staff must be trained by a supervisor who has read and understands the instructions.
- Trainees should have time to ask questions and be supervised during cleaning.
- Hillrom recommends cleaning and disinfecting between patient uses and regularly for extended stays.
- Some hospital fluids may stain; remove temporary stains with a lightly dampened cloth.
Cleaning and Disinfection Overview:
- Cleaning removes soil; disinfection kills microorganisms.
- Use microfiber cloths and a soft bristle brush for small holes (e.g., Q-Link II).
- Replace cloths when soiled and between steps.
Step 1: Cleaning
- Unplug the mains (AC power source).
- Remove visible soil with a warm water-moistened cloth and an approved cleaner/disinfectant. Do not use dripping wet cloths. A soft bristle brush can help with stubborn areas.
- Wipe the entire lift from top to bottom, paying attention to seams and crevices. Key areas include: Lift strap, Emergency lowering/raising, Emergency stop, Emergency stop cord, Mechanical emergency lowering, Sling bar, Hand control.
- Ensure the lift strap is dry after cleaning.
Cleaner/Disinfection:
- Remove all visible soil before proceeding.
- Use a new cloth soaked in cleaner/disinfectant, applying firm pressure. Use clean cloths as needed.
- Clean the following: Hand Control, Lift Motor, Lift Strap, Slingbar, Scale (if applicable), Power cord, Connection points, and any soiled rail parts.
- Replace any damaged items.
Step 2: Disinfection:
- Refer to "Application of commonly used Cleaning / Disinfectants on Liko products" for suitable disinfectants.
- Follow manufacturer's instructions.
- Ensure surfaces remain wet with the cleaner/disinfectant for the specified contact time, rewetting as needed.
Note: If using bleach with another disinfectant, rinse with clean water before and after bleach application.
Restrictions: The lift, hand control, and lift strap have specific cleaning restrictions (e.g., not to be cleaned with CSI, Viraguard, Oxivir Tb, etc.). Refer to the detailed table for specific product compatibility.
Cleaning/Disinfectant Compatibility Table:
Chemical Class | Active Ingredient | pH | Cleaners / Disinfectant | Manufacturer | May not be used on the following items |
---|---|---|---|---|---|
Quaternary ammonium chloride | Didecyl dimethyl ammonium chloride (8.704%), Alkyl dimethyl benzyl ammonium chloride (8.19%) | 9.0-10.0 | Virex II (256) | Johnson/Diversey | Foot rest for Sabina sit-to-stand lift and Roll-On support for raising |
Quaternary ammonium chloride | Alkyl dimethyl benzyl ammonium chloride (13.238%), Alkyl dimethyl ethylbenzyl ammonium chloride (13.238%) | 9.5 | HB Quat 25L | 3M | The lift straps for Golvo mobile lift and overhead lifts |
Accelerated Hydrogen Peroxide | Hydrogen Peroxide (0.1-1.5%), Benzyl Alcohol (1-5%) | 3 | Oxivir Tb | 3M | - |
Phenolic | Ortho-Phenylphenol (3.40%), Ortho-Benzyl-para-Chlorophenol (3.03) | 3.1 +/- 0.4 | Wexcide | Wexford Labs | The lift straps for Golvo mobile lift and overhead lifts |
Bleach | Sodium hypochlorite | 12.2 | Dispatch | Caltech | Hand controls for all lifts |
Alcohol | Isopropyl alcohol (70%) | 5.0-7.0 | Viraguard | Veridien | Viking mobile lift, Liko M220/M230 mobile lift, Uno, Sabina, Golvo, LikoLight, Roll-On, Likorall, Multirall overhead lifts; Foot rest for Sabina sit-to-stand lift and Roll-On support for raising |
Quaternary ammonium | n-Alkyl dimethyl benzyl ammonium chlorides (0.105%), n-Alkyl dimethyl ethylbenzyl ammonium chlorides (0.105%) | 11.5-12.5 | CSI | Central Solutions Inc. | The lift straps for Golvo mobile lift and overhead lifts |
Benzyl-C12-18-alkyldimethylammonium, chlorides | Benzyl-C12-18-alkyldimethylammonium, chlorides (22%) | approx 8.6 | Terralin Protect | Shülke | Control box for all mobile lifts |
Organic peroxide (type E, solid) | 2-Phenoxyethanol (20%), Tridecylpolyethylenglycolether (15%), Propan-2-ol (8%), Magnesium monoperoxyphtalate hexahydrate (50-100%), Anionic surfactant (5-10%), Nonionic surfactant (1-5%) | 5.3 | Dismozon Pur | Bode | The lift straps for Golvo mobile lift and overhead lifts |
Ethanol | Hydrogen peroxyde (2.5-10%), Lauryldimethylamine oxid (0-2.5%), Ethanol (2.5-10%), Adipic acid (10-30%), Amorphous silica (<1%) | 7 | Anioxy-Spray WS | Anios | - |
Troclosene sodium | Sodium Toluene sulphonate (5-10%), Troclosene sodium (10-30%) | 4-6 | Chlor-Clean | Guest Medical Ltd | The lift straps for Golvo mobile lift and overhead lifts |
*) Or equivalent
Inspection and Maintenance
Daily Checks:
- Inspect for external damage.
- Check sling bar attachment.
- Check lift strap for wear and twists.
- Verify latch functionality.
- Check lift movement operation.
- Ensure emergency lowering functions correctly.
- Verify mechanical emergency lowering and lifting height setting.
- Charge batteries daily and check charger function.
Clean the lift with a moist cloth. Refer to the "Cleaning and Disinfection" chapter for details. Do not expose the lift to running water.
Service:
- A periodic inspection is required at least once per year.
- Service, repair, and maintenance must be performed by authorized personnel using original Liko spare parts, following the Liko Service Manual.
- Service activities must not be performed with the patient in the lift.
Service Agreement: Hillrom offers service contracts for maintenance and regular inspection.
Expected Life Time:
- Product: 10 years (with proper handling, servicing, and inspection).
- Handcontrol: 2 years.
- Battery: 3 years.
- Lift strap: 5 years.
Transport and Storage:
- Activate emergency stop during transport or long-term storage.
- Storage environment: -10°C to +50°C (14°F-122°F), 20-90% relative humidity, 700-1060 hPa atmospheric pressure.
Product Changes: Liko continuously develops products and reserves the right to make changes without prior notice. Contact Hillrom for upgrade information.
Design and Quality: Liko is ISO 9001 and ISO 13485 certified for medical devices, and ISO 14001 for environmental standards.
Notice to Users/Patients in EU: Report any serious incidents to the manufacturer and the competent authority of the Member State.
Golvo, Liko, Likorall, Sabina, and Viking are trademarks of Baxter International Inc. or its subsidiaries. Other trademarks are property of their respective owners.
Contact Information
Liko AB,
Nedre vägen 100
975 92 Luleå, Sweden
+46 (0)920 474700
Liko AB is a subsidiary of Hillrom Holdings Inc.
Website: www.hillrom.com