DHG SystemRoMedic 56-304 User manual

IFU no: 928 rev. 2 2022-03-01
Max User Weight: 150 kg / 330 lbs
Bure Space Instructions for use – English
Bruksanvisning – Svenska

Table of contents
English............................................................................................... 4
Svenska............................................................................................19

3IFU
Product Overview
56-304
56-304-B/0-FKN_R
56-304-B/0-FKH_R-PU
56-304-B/0-FKH_R-PL-PU-R
56-304-B/0-PU
56-304-B/1-PL-PU
56-304-PLUS
56-304-PLUS-PU
56-304-PLUS-RED
56-304-PU
56-304-RED
56-304/100
56-304/75
56-304/75-B/0
56-304/75-B/0-FKH_R-PS-PU
56-304/75-B/0-FKN_R-PU
56-304/75-B/1
56-304/75-PLUS
56-304/75-PLUS-PU
56-304/75-PU
56-307
56-307/100
56-307/75
56-307-B/1-PU
56-307-B/1-PU-RED
56-307-PU
56-307/LOW

4IFU
Contradictions
• The device may not be used by patients above the maximum weight indicated on the label of the device.
Precautions
• Check that the device is used on a dry and flat surface.
• Check the device is correctly mounted/assembled before its first use.
• Check the device after every folding/disassembly after any transport.
• Check height adjustment and leg spreading motions and inspect the actuators or gas pistons full ranges.
• Activate the brakes whenever the device is not in use.
• Check the function of the brakes before use.
• Inspect the device regularly to detect any signs of damage. If there are any visible signs of damage, contact
Direct Healthcare Group Customer Service.
• Check that the hand control does not show signs of wear before every use.
• Check that the hand control markings are in accordance with the lifting functions.
• Check the battery status of an electrically operated model before using the device.
• Warranty applies only if repairs or alterations are made by personnel who are authorized by Direct Healthcare
Group.
• Ensure that there are no obstacles or people in the way of the device, when moving.
• Handle batteries with care. Do not drop.
• Use only batteries and cables that are intended for the device as instructed by the manufacturer.
• Verify that potential accessories that might be used are properly attached to the device before use.
• Low speed is recommended when moving with the device.
• Take care not to drive the device over thresholds with high speed or force. Approach the threshold with lower
speed and communicate the coming threshold to the user.
• In case of an electrical model of the device, check that the hand control does not show signs of wear before
every use
• Keep the instructions for use together with the product so that it can be used as a reference if necessary.
Instructions for use - English
Bure Space
Bure Space is a walker that has been specifically designed for the orthopaedics departments and situations where
patients require extra leg room to get up closer to wheelchairs or similar. Bure Space is available with electrically oper-
ated or hydraulic height adjustment.
1. Intended use
Walkers are indoor, movable and portable assistive aids, which together with approved accessories are intended to
be used for transfer from sitting to standing positions, and walking training. Walkers are to be used by persons with
reduced muscular strength, who shall be able to stand and perform simple leg movements. Walkers are to be used
for leaning on when walking and standing during early mobilisation training. Walkers and accessories are intended for
indoor use only in Home Healthcare environment and Professional Healthcare facility environment.
The Bure Space is intended to be used in orthopaedics department and situations where patients require extra leg
room to get up closer to wheelchairs or similar.
2. Contraindications, Precautions, Warnings

5
IFU
• Beware of moving parts during usage.
• Peform a risk assessment on the user before using the Walker to ensure they can stand and peform simple
movements.
Warnings
• The device may not be used by infants, children or adults who are 146 cm or shorter.
• The caregiver must be able to read and understand the Manual/IFU of the product.
• Caregiver: Never use the device if you have not had a proper training on how to use the device including the
accessories.
• Maintenance/Service staff: Never maintain the device if you have not had a proper training on how to use and
maintain the device including the accessories.
• It is important to use only approved accessories to prevent unintended detachment of components and
subsequently a fall that may lead to patient injury.
• Use careful and gentle maneuvers when moving the device.
• Perform maintenance/service of the device, according to the instructions in the IFU (Instruction for use), at
least once every 12 months.
• No parts of the device shall be serviced, while the device is in use
• Accessories must be properly fitted and tested in relation to the user’s needs and functional ability.
• Special care must be taken when using strong electrical power sources such as diathermy and the like so
that diathermy cables are not placed on or near the device. In case of doubt consult with a Direct Healthcare
Group representative.
• When lifting the device, only use the denoted handholds. At least two people are required for lifting the
device.
• Do not leave a patient unattended when the device is being used.
• The device can not be used by patient alone.
• Never move the walker by pulling on the actuator device or gas piston.
• The device must not be lowered into water.
• The device must not be cleaned using steam.
• The device must not be left or stored in a damp or humid environment.
• The device must not be charged in a wet room.
• The device must not be used outdoors, only indoors.
• To avoid the risk of electric shock, this equipment must only be conected to a supply mains with protective
grounding.
• No modification of this equipment is allowed
• Do not modify this equipment without authorisation of the manufacturer.
• If this equipment is modified, appropriate inspection and testing must be conducted to ensure continued safe
use of this equipment.
• Do not use the device while it is charging.
• Do not use the device if any of the cables shows signs of wear and tear.
• Do not put the device in direct sunlight as it may get hot.
• Do not run over the cables with the walker or other devices.
Always make sure that you have the correct version of the manual. The most recent version of all manuals are
available for downloading at/from our website: www.directhealthcaregroup.com.
Always read the user manual

6IFU
3. Using Bure Walker
Standing up and walk training
1. Ask the user to sit on the edge of the bed or chair. Bring out the walking table and place it in front of the user.
Lock the brakes on the wheels.
2. Ask the user to place their arms on the armrests. If necessary, ask the user to move forward on the seat base
so that the user reaches the handles.
3. Ask the user to lean forward. To start raising the walking table, press the UP button on the controller. Raise
the walking table to a desired height.
4. Unlock the brakes. Adjust the height of the walking table to a desired position
5. Assist the user while walk training.
Before first use:
• Inspect the packaging for any damage.
• Check for correct product being delivered.
• Check to ensure that the device is free from damage.
• Check if all the parts/components are included in the package.
• Check if all approved accessories are included in the package.
• Check if Product Quality Approval document is included in the packaging. Save this document for future
contact with manufacturer.
• Make certain the device is properly assembled.
• Check lifting function and bottom-frame adjustment function.
• Check if it is possible to move the device in all directions.
With gas piston:
1. Ask the user to sit on the edge of the bed or chair. Bring out the walking table and place it in front of the user.
Lock the brakes on the wheels.
2. Raise the walking table by pressing the handle on the gas piston.
3. Ask the user to lean forward, grap the armrests and stand up.
4. Adjust the height of the walking table to a desired position

7IFU
4. Using Bure Walker with Gait Training Kit 56-388
Top view
Front
Back
• The gait support harness has four blue straps with a plastic buckle allowing for adjustments in length, having
steel carabiner clips at the ends to be fasten to the gait walker. The carabiner clips on to the metal mounts
placed under the table of the Gait walker.
• Apply the gait walker support harness by clipping on the two front carabiners to the front mounters, one on
each side of the table.
• Place the user standing up in the Gait walker. Pull back the harness in between the legs and clip on the
carabiners to the back mounters, one on each side of the table. Adjust the harness to the user by pulling in
the back strap loops.
• Observe! Intended use of the Gait trainer support harness is to practise walking. It is not a sitting or lifting aid.
Standing Plate
Attach standing plate by hooks on the main frame of the walker

8IFU
Adjust the height with the aid of the remote control UP and DOWN arrows.
Handset Plus has charge indicator / battery (low, medium, high) and Service indicator (see
further under “Hand Control Plus”).
Adjusting the Handles
To adjust handles to the desired position; loosen screw, adjust handle, tighten
screw.
Left and Right Adjustment of Armrests
The armrests can be adjusted sideways for optimal support; loosen screw, adjust
armrest, tighten screw.
NOTE: The rear attachments on the frame/armrest are interchangeable (left with right and
vice versa) to provide different widths. The locating pins on the cushion’s underside/rear
can also be moved. These adjustment capabilities make customisation possible.
Locking/Unlocking Castors wheels
The device is equipped with lockable / braked castor wheels. Lock the wheels by
pressing the green pedal brake down with your foot. To release the break, press the
green protruding part with your foot.
Raising/Lowering the Frame
Hand Control Plus
**1. Service indicator – flashes red after 11 months’ operation.
Constant light (red) after 12 months’ operation.
The indicator is a reminder to review the maintenance instruction (see Maintenance
Instructions). This should be done at least once every 12 months.
Reset: hold down buttons <2a> + <2b> for at least 30 seconds. **The indicator will go out
around 30 seconds after the hand control is activated (battery conservation function).
1
2a 2b

9
IFU
Battery Charging
Battery charging must take place when the device is not in use.
Charging starts automatically when power plug is connected to 230V wall socket. Green light on the control box will
turn on, once the power plug is connected.
• The LED flashes green during charging.
• ON/OFF: To use the product, press ON.
• The green lamp will begin to flash.
• Use the OFF button (hold down for 5 s) to switch off the battery if the product
• will not be used for an extended period.
• The LED will shows a constant green light when the battery is fully charged.
• When the battery is in normal state/in operation, the LED flashes green at REGULAR intervals, namely 0.5 s
ON, 4 s OFF.
• When the battery requires charging (remaining charge <25%) the LED will flash orange/red at REGULAR
intervals, namely 0.5 s ON, 4 s OFF.
NOTE: The battery has an in-built device that automatically switches it off when remaining charge is <20%. The
LED is then extinguished. The battery must now be fully charged before the electronics can be used again.
Control box
The control box cover can be opened by using a screwdriver or similar; refer to the intstructions which are sitting on
the control box.
NOTE: Make sure that plugs are connected to the correct sockets otherwise the actuators can be damaged.
1. Connector for actuator up / down.
2. Hand control connector.
3. Battery outlet.
4. Connector for mains cable. NOTE: The mains cable must
ALWAYS be connected to the control box for IP protection to be valid.
Trouble shooting
If the lifting function cannot be activated, check the following:
• That all cables are properly and securely connected,
Pull out the contact and plug it in again firmly.
• That battery charging is not in progress.
• That the battery is charged.
If the device is not working properly, contact your distributor.
If the device makes unusual noises:
• Try to determine the source of the sound. Take the device out of operation and contact your distributor.
1
2
3
4

10 IFU
Accessories
Art. Nr. Description
56-339-1-0 Handbrake kit/2 handles
56-339-1-1 Handbrake kit/One-handed brake
56-336-4 Oxygen holder
56-337 Side support, adjustable
56-338 Drip rod complete with attachment
56-389 Soft basket with attachment
56-352 Lower Leg Support

11
IFU
5. Maintenance
The device must undergo thorough inspection at least once per year. Inspection must be performed by authorised
personnel and in accordance with Direct Healthcare Group’s instructions.
Repairs and maintenance may only be done by authorised personnel using original spare parts.
Check that Action if a problem is noticed
General
The Walker feels firm/free from play.
The Walker does not rattle during manoeuvres.
The Walker is level and all of its castors are in
contact with the floor.
The Walker is not dirty.
Clean with lukewarm soap solution or alcohol-based cleaning
agent (no petroleum products).
Armrests
Armrests are intact and clean.
Armrest widening is functional. Clean; replace if damaged. Replace lock knob.
Fit lock screws/plates as required.
Handle
Grips are not damaged/dirty.
Handle adjustment is functional. Clean with lukewarm soap solution (no petroleum products). Replace handle grips.
Fit lock screws/plates as required.
Electronics
Check that the charging cable is connected to
the control box.
Check that the hand control is connected to
the control box.
Check that the battery, actuators and control
box are not loose.
If any part needs to be replaced refer to the wiring diagram in
the control box wiring section.
Fit new charging cable; this must always be connected to the
control box.
Connect or fit new hand control as required.
Tighten; replace with new fasteners as required.
Height adjustment
Raising and lowering are functional.
The Walker feels stable at maximum settings.
There is no play between the vertical frame
and bottom frame.
Height adjustment clamps lock.
The electric actuator fitting must be free from
play.
Height adjustment via hand control is
functional. The electric actuator must run
smoothly at a constant speed.
Fit new guide sleeves (in frame) or end plugs (in chrome
tubes) as required.
Tighten all lock bolts.
Replace clamps.
Tighten the attachment fitting concerned; replace bolts/lock
nuts as necessary.
Check that the battery/hand control/ actuator are connected in
accordance as in the control box wiring section.
Charge the battery.
The part list shows the design and which fasteners must be
checked.
Frame parts
There is no mechanical damage.
There are no scratches.
End plugs/lower frame fitted
If mechanical damage is present, contact DHG Customer
Services.
Touch up as necessary.
Fit new end plugs.
Castors/brakes
Castors roll easily/tread not damaged.
The castors are firmly fastened to the lower
frame.
Castor brakes functional on all castors.
Handbrake functional.
Clean or replace castors.
NOTE! Castors are always fixed to the lower frame with thread
locker or lock nuts. The castors are sealed and we do not
recommend their dismantling; instead, replace the whole
castor assembly.
Tighten the castor bolt and fit locking nut or use thread locker
(depends on model).
Replace castor assembly.
Adjust the brake or fit new castors.
Power cord may only be replaced by DHG service personnel or technical personnel trained by DHG.
DHG can provide upon request neccessary technical information in order to assist maintenace and repair of the
device.

12 IFU
Storage and transportation
The walker should be transported and stored in 5 ° C to 50 ° C and in normal humidity, 20% to 80% non-condens-
ing. The air pressure should be between 700 and 1060 hPa. Leftmost symbol indicates storage and transportation.
Let the walker reach room temperature before the batteries are charged or the walker is used. The walker should
not be stored so that it is exposed to dust, or so that the battery or gas piston is exposed to direct sunlight.
Operation
The operating environment should be 5 °C to 40°C, relative humidity 20% to 80% non-condensing, and atmo-
spheric pressure 700 to 1060 hPa. See also Technical specification below. Leftmost symbol indicates operating
condition.
Cleaning and disinfection
After every use:
Clean the walker armrests and handles. Wipe using a mild soap solution/surface disinfectant. However, the product
is not corrosion proof.
Weekly and possibly more often depending on frequency of use:
If necessary, clean the whole walker with a cloth with warm water or a soap solution and check that the castors
are free from dirt and hair. The electronic components (battery, control box, hand control, actuators, cables) should
be cleaned with a damp cloth only. To avoid degreasing of the piston rods, the actuators should be retracted to
minimum stroke and without load before cleaning. Ensure that the device is dried thoroughly after cleaning.
If disinfection is needed:
70% ethanol, 45% isopropanol or similar should be used.
Do not steam clean due to risk of corrosion.
Do not use cleaning agents containing phenol or chlorine, as this could damage the materials.
With enviroments with high risk of infections use the walker with PU-cushions (Accessory number 57-361-L
and 57-361-R)
Recycling/Disposal
When the product is no longer usable it should be recycled in accordance with legislation and regulations in the
country concerned. All electrical parts including batteries must be removed and recycled as electrical components.
Ask your local recycling station for further information about how the different materials in the product (metals,
plastics, electronics) should be recycled. Used batteries can also be returned to Direct Healthcare Group or a Direct
Healthcare Group distributor for recycling.
40°C
5°C
50°C
-10°C
1060
hPa
700
hPa
1060
hPa
700
hPa
%
80%
20%
%
80%
20%

13IFU
6. Technical Specifications
Control box TiMotion, Voltage 220V-240VAC, 50Hz, 1250mA/24VDC, 70VA, IP66, Class II (Dou-
bled insulated)
Batteries TiMotion, 24 V - 4A, 96Wh, Rechargeable Li-Ion Battery, IP66, Cable length 600mm,
Duty cycle: 10%, Max. 2min. ON/18 min./OFF
Actuator 12VDC, Max 8,0A, Push: 2000N, Self-locking capacity (min): 1000N, Stroke 400mm
+/-2 mm, IP66.
Duty cycle: 10%, Max. 2min.ON/18min. OFF
Hand Control Cable length straight 300mm + coiled 400 mm, IP66
IP class IPX5
Material Steel
Castors 125/100/75mm
Weight 20 kg
Expected Service life 8 years
Max patient weight 240 kg / 529 Ibs
Operating environment 5 °C to 40°C, relative humidity 20% to 80% non-condensing, and atmospheric
pressure 700 to 1060 hPa.
Storage and transportation
environment
5 °C to 50 °C, relative humidity 20% to 80% non-condensing, and atmospheric.
Environment pressure 700 to 1060 hPa.
Height 125 mm wheels model minimum 900 mm and maximum 1300 mm
100 mm wheels model minimum 880 mm and maximum 1280 mm
75mm wheels model minimum 850 mm and maximum 1250 mm
Length 850 mm
Width 775 mm
Turning Width 125 mm wheels: 1158 mm, 100 mm wheels: 1130 mm, 75 mm wheels: 1130 mm
Materials in contact with
human skin
Materials that user and operator/caregiver are exposed to during usage of the pro-
duct for prolonged time:
Poroflex (synthetic leather cushions) Px
Polyurethane (on PU cushions) P
Dryflex (handles) P
PA6 + 20% GF (brake lever) P
Hand control C X
Applied parts: Armrest P
Handles P
Knee pad P
Foot rest support P
Foot rest support clamps C
Handles adjusting knobs C
Hand controller and its holder. C
Handles to adjust the armrest width. C
Hand control C
Charger C
Charger cable C
Footplate
xP - patient, X C - caregiver

14 IFU
7. Parts
NO. PART NO. DESCRIPTION NO. PART NO. DESCRIPTION
1 58-373 Control box 220V Digital Li-On
TiMotion Bure
16 57-810 Screw MC6S M8x45
2 58-377 Actuator T-Motion
2000N/5200rpm, Bure
17 57-811 Serrated lock washer M16
3 58-389 Battery box 4.0 Ah TBB5/Li-On 18 57-917 Wing nut
4 58-335 Telescopic Inner pipe 19 57-925 Endcover pipe 39mm black
5 57-421 Telescope inner pipe Bushing 20 56-308 Cable holder Bure charger
6 57-422 Telescope inner pipe Tube 21 57-808 Pin bolt M6x25 8.8
7 57-747 Plug dome plastic 25dia 22 57-792 Washer Cushion
8 57-049 Castor wheel 125mm brake 23 57-848 Nordlock 10,7x21x2,5
9 57-307 Protective cover plastic 24 57-918 Washer 6,5x15x10
10 57-310 Middle frame bushing 25 57-357-L Armrest Cushion Low Left
11 57-803 Locking washer M10
6.1x11.8x1.6
26 57-357-R Armrest Cushion Low Right
12 57-804 Screw MC6S M8x35 27 57-919 Star knob handle
13 57-805 Washer BRB 6,4x12x1,6 28 58-331 Cover actuator rod
14 56-353 Bure Handle assy 29 58-374-
X1
Hand control TiMotion TH10
15 57-806 Washer 8.4x16x1.5 30 58-326 Spiral Cord EUR - T-Motion, Bure

15IFU
OPTIONS
NO. PART NO. DESCRIPTION
1 57-361-L PU Arm support cushion Bure left
2 57-361-R PU Arm support cushion Bure right
357-051 Wheel w/o brake 75mm
4 56-387 Wheel with brake 75 mm
5 57-319 Wheel with brake 100mm
6 56-357 Wheel w/o brake 100mm
7 56-360 Wheel w/o brake 125mm
8 56-339-1-0 Handbrake kit/2 handles
8 56-339-1-1 Handbrake kit/One-handed brake
9 Multiple options Footplate Bure Ortho/Space
56-305 Touch-up paint Bure, Silver 8
58-306 Touch-up paint Bure, Dark grey RAL 7021

16 IFU
8. Product label
UDI (Unique Device Identification) can be found within
the barcode human readable text. It contains:-
(01) EAN code
(11) Date of Manufacture. The date is in the format
YYMMDD Y = Year, M = Month and D = Date.
(21) Serial Number displayed as five digit code.

17
IFU
This product complies with the
requirements of the Medical Device
Regulation 2017/745
Visual Inspection
Medical Device Read the manual
Caution Product Code
Legal manufacturer
Direct Healthcare Group
Sverige AB
Batch Code
Type BF applied parts, according to the
degree of protection against electric shock
The device is intended for indoor use
WEEE Symbol
May not be discarded in domestic waste
Class II Equipment
Duty Cycle:
1 min in active (ON) mode.
19 min in rest (OFF) mode.
Maximum patient weight
Walker Height Walker Width
Do not step on the device Refer to instruction manual (IFU)
27333 240
Mass
Weight (mass) of the device, the Maximum Patient Weight,
and total sum. All in kg.
9. Table of Symbols
10. How to report a serious incident
Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the
MHRA or another competent authority of the country in which the user and/or patient is established.
UK
[e-mail]
T: [phone]
F: [phone]
Other:
[e-mail]

18 IFU
Wheel diameter A: Turning
width
B: Armrest
height
B: PU Armrest
height
C: Wheel area
diameter
D: Length
125mm 1158 900-1300 870-1270 218 850
100mm 1130 880-1280 850-1250 190 835
75mm w brake 1130 850-1250 820-1220 188 830
75mm 1084 840-1240 810-1210 145 814
11. Dimensions

19
IFU
1. Avsedd användning
Gåbord ska enbart användas inomhus och på plant underlag. Gåbord är ett hjälpmedel, som tillsammans med
godkända tillbehör är avsedda att användas för förflyttning från sittande till stående positioner och gångträning.
Gåbord ska användas av personer med nedsatt muskelstyrka, som ska kunna stå och utföra enkla benrörelser.
Gåbord ska användas för att luta sig mot, när brukaren går och står under tidig mobiliseringsträning. Gåbord och
tillbehör är avsedda att användas i hemsjukvårdsmiljö och professionell vårdinrättning.
Kontraindikationer
• Produkten får inte användas av en brukare vars vikt överstiger den maximala brukarvikt som anges på
produktens etikett
Försiktighetsåtgärder
• Kontrollera att produkten används på en torr och plan yta.
• Kontrollera att produkten är korrekt monterad/ihopsatt före den första användningen.
• Kontrollera produkten efter att den har varit ihopfälld /demonterad efter transport.
• Kontrollera höjdjustering och benspridningsrörelser och inspektera ställdonens eller gasfjäderns fulla
rörelseomfång.
• Aktivera bromsarna när produkten inte används.
• Kontrollera bromsarna före användning.
• Inspektera produkten regelbundet för att upptäcka tecken på skada. Om det finns några synliga tecken på
skada, kontakta Direct Healthcare Groups kundtjänst.
• Före varje användning av en elektrisk modell av produkten, kontrollera att handkontrollen inte visar tecken på
slitage.
• Kontrollera att markeringarna på handkontrollen överensstämmer med lyftfunktionerna.
• Före varje användning av en elektrisk modell av produkten; kontrollera batteristatus.
• Garantin gäller endast om reparationer eller ändringar görs av personal som är auktoriserad av Direct
Healthcare Group.
• Se till att det inte finns några hinder eller människor i vägen för produkten när brukaren förflyttar sig med hjälp
av produkten.
• Hantera batterier varsamt. Tappa inte.
• Använd endast batterier och kablar som är avsedda för produkten enligt tillverkarens anvisningar.
Bruksanvisning - Svenska
Bure Space
Bure Space är ett gåbord som är speciellt framtagen för ortopediavdelningar och situationer där patienter behöver
extra benutrymme för att komma närmare med rullstolar eller liknande. Bure Space finns med elmanövrerad eller
hydraulisk höjdjustering.
2. Kontraindikationer, försiktighetsåtgärder och varningar

20 IFU
• Kontrollera att potentiella tillbehör som kan användas är korrekt anslutna till enheten före användning.
• Låg hastighet rekommenderas när du använder produkten.
• Var försiktig så att du inte kör produkten över en tröskel med hög hastighet eller kraft. Närma dig trösklar med
lägre hastighet och uppmärksamma brukaren när ni närmar er en tröskel.
• Förvara bruksanvisningen tillsammans med produkten så att den kan användas som referens vid behov
• Vid en elektrisk modell av enheten, kontrollera att handkontrollen inte visar tecken på slitage före varje använd-
ning. Förvara bruksanvisningen tillsammans med produkten så att den kan användas som referens vid behov.
• Se upp för rörliga delar under anvädning.
• Genomför en riskbedömning med en brukare innan ni använder ett gåbord. Säkerställ att brukaren kan stå
och göra enkla rörelser med ben.
Varningar
• Enheten får inte användas av spädbarn, barn eller vuxna som är 146cm eller kortare.
• Vårdgivaren måste kunna läsa och förstå produktens bruksanvisning och användarinstruktioner.
• Vårdgivare: Använd aldrig enheten om du inte har fått ordentlig utbildning i hur du använder enheten inklusive
tillbehören.
• Service- och underhållspersonal: Underhåll eller modifiera aldrig enheten om du inte har fått ordentlig
utbildning i hur du använder och underhåller enheten inklusive tillbehör.
• Det är viktigt att endast använda godkända tillbehör listade i bruksanvisningen för att förhindra att
komponenter lossnar oavsiktligt, då detta medföra ett fall och patientskada.
• Manövrera mjukt och försiktigt när du jobbar med produkten.
• Utför underhåll/service av enheten, enligt instruktionerna i bruksanvisningen (bruksanvisning), minst en gång
var 12:e månad.
• Inga delar av enheten ska servas när enheten är i bruk
• Tillbehören måste vara ordentligt fastsatta. De bör testas i förhållande till användarens behov och
funktionsnivå.
• Särskild försiktighet måste vidtas vid användning av starka elektriska kraftkällor som används vid till exempel
diatermi och liknande så att diatermikablar inte placeras på eller i närheten av enheten. Vid tvivel, rådgör med
en representant för Direct Healthcare Group.
• När du lyfter produkten ska du endast använda de angivna handfästena. Minst två personer krävs för att lyfta
enhet.
• Lämna inte en patient utan uppsikt när enheten används.
• Enheten kan inte användas enbart av patienten.
• Flytta aldrig lyften genom att dra i ställdonet eller gaskolven.
• Produkten får inte sänkas ner i vatten.
• Produkten får inte lämnas eller förvaras i miljö med hög luftfuktighet.
• Produkten får inte rengöras med ånga.
• Produkten får inte laddas i ett våtrum
• Produkten får inte användas utomhus, endast inomhus.
• För att undvika risk av en elektrisk chock, gåbord kan endast kopplas mot elektrisk källa med jord.
• Ingen modifiering av denna utrustning är tillåten.
• Modifiera inte den här utrustningen utan tillverkarens godkännande
• Om denna utrustning modifieras måste lämplig inspektion och testning utföras för att säkerställa fortsatt säker
användning av denna utrustning.
• Använd inte enheten under laddning.
• Använd inte enheten om någon av kablarna visar tecken på slitage.
• Utsätt inte enheten för direkt solljus då den kan bli upphettad
• Kör inte över kablar med gåbordet eller annan utrustning.