Liko

Liko Mobile Patient Lifts and Sit & Stands

Golvo Instructions for Use March 2011

Instructions for Use

16 Pages

Table of Contents Safety Instructions... 2 Definitions... 3 Technical Data... 3 Dimensions... 4 Assembly... 5 Disassembly... 7 Operation... 8 HandControl IR... 10 Operation Panel... 10 Charging the Batteries... 11 Maximum Load... 12 Recommended Lifting Accessories... 12 Simple Troubleshooting... 15 Inspection and Maintenance ... 16 NOTE! This instruction guide contains important information for users of the product. All those who use the product should review and fully understand the contents of the instruction guide. Remember to keep the instruction guide in a place where it is always available to those using the product.  Safety Instructions Before using the first time make sure that: • the lift is assembled in accordance with the assembly instructions • the lifting accessory is properly attached to the lift • the batteries have been charged for at least 5 hours • you have read the instruction guides for the lift and lifting accessories • personnel using the lift are informed of the correct operation and use of the lift. Before lifting, always make sure that: •	the lifting accessories is selected appropriately in terms of type, size, material and design with regard to the patient’s needs • the lifting accessories are not damaged • the lifting accessory is correctly attached to the lift • the lift strap is not twisted or worn and can move in and out of the lift • the lifting accessory hangs vertically and can move freely • the lifting accessory is correctly and safely applied to the patient in order to prevent injuries • the latches are intact; missing or damaged latches must always be replaced •	the sling’s strap loops are correctly connected to the sling bar hooks when the sling strap is extended, but before the patient is lifted from the underlying surface. Never leave a patient unattended during a lifting situation!  		 Golvo 8000/8008/8008 LowBase™ have been tested by an accredited testing institute and fulfil the requirements specified in the Medical Device Directive for class 1 products (MDD 93/42/EEC). Golvo 8000/8008/8008 LowBase™ complies with the requirements in EN ISO 10535, IEC 60601-1, IEC 60601-1-2, ANSI/AAMI ES60601-1 and CAN/CSA C22.2 no. 60601-1 Under no circumstances must the lift be modified. If you have any questions, please contact Liko. Particular care must be observed when using strong sources of potential disturbance, such as diathermy, etc, so that diathermy cables are not positioned on or near the lift. If you have questions, please consult the responsible assistive-device technician or the supplier. The lift must not be used in areas where flammable mixtures may occur, for example in areas where flammable goods are stored. Golvo • 7EN140105-02    w w w . l i k o . com
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File Name: Liko - Golvo Instructions for Use March 2011 - 2011-03.pdf

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