Rehamedi Medior User manual

www.rehamedi.de

Mobilizer Medior

Instructions for use

Mobilizer Medior

Table of contents Information on the

instructions for use

Manufacturer

Reha & Medi Hoffmann GmbH

Debyestraße 5

04329 Lei zig

Germany

Tel. +49 341 / 39284960

[email protected]

SRN: DE-MF-000007034

www.rehamedi.de

Version: 4

Date of issue: 26.04.2023

Language: english

Validity range: Mobilizer Medior

Article number: 6020412

1. foreword and general information .........................3

1.1 Co yright ........................................................ 4

1.2 Disclaimer ....................................................... 4

1.3 Denition of grou s of ersons....................... 5

2. descri tion, ur ose, denition ......................6

2.1 Indication ....................................................... 7

2.2 Contraindication.............................................. 7

3. Permissible o erating conditions /

lace of use.....................................................8

4. Dimensions......................................................8

5. Safety instructions ........................................10

5.1 Ex lanation of symbols and notes................ 10

5.2 Basic safety information ...............................10

5.3 O erational ca ability ................................... 12

5.4 Products with battery.................................... 13

6. Height adjustment.........................................14

7. Backrest adjustment .....................................14

8. Hand control..................................................15

8.1 Function keys................................................ 15

8.2 Programme buttons ...................................... 15

9. Main switch ...................................................16

10. Transfer .........................................................16

11. Armrests........................................................17

12. Footste ........................................................18

Positioning ................................................... 18

electric footrest adjustment ......................... 18

13. Driving and braking .......................................19

14. CPR function.................................................19

15. Angle dis lay.................................................19

16. Battery change..............................................20

17. Product care note..........................................21

18. Re rocessing ................................................21

Cleaning and disinfection ............................. 21

19. Re-use...........................................................21

20. Equi ment o tions........................................22

Headrest, xing............................................. 22

Locking the armrests .................................... 22

Table with u holstery .................................... 22

Side bar......................................................... 22

Infusion stand ............................................... 23

Stra s............................................................ 23

Akku .............................................................. 23

Vibrationsmodul ............................................ 23

21. Warranty........................................................24

22. Dis osal ........................................................24

23. Technical data ...............................................24

23.1 IP rotection classes and

tem erature ranges....................................... 25

23.2 The ty e late ............................................... 26

1. foreword and general information

Dear customer,

Thank you for choosing a roduct from Reha & Medi Hoffmann GmbH. These instructions

for use rovide you with all the im ortant information and notes on the Mobilizer Medior. It

is also intended to make it easier for you to become acquainted with the roduct and to

rovide instructions for its ro er use and safe o eration.

Please read this manual carefully and completely before using your Mobilizer Medior.

Keep them handy for future reference.

All directions are indicated looking from the rear of the roduct in the direction of travel, as

shown in Fig. 1.

Assembly / Mounting

Assembly or mounting is not required. Mobilizer Medior is delivered ready for use. Before

rst use, the batteries must be charged.

If, des ite careful study, further information is required, lease do not hesitate to contact us.

You will nd our contact details at the beginning of these instructions for use. Online you

will nd all documents in digital form at www.rehamedi.de.

Fig. 1: Basis for directional/ lateral indications (Fig.

shows Mobilizer Medior with vibration module

LEFT RIGHT

DIRECTION OF TRAVEL

Instructions for use Mobilizer Medior

1.1 Copyright

These o erating instructions, including all their arts and illustrations, are rotected by co-

yright. The rights to translation, re rinting, extraction of ictorial re resentations as well as

re roduction and storage in data rocessing systems are reserved, even if only excer ts are

used. The use in lectures or ublication in media, in articular in ublications, also in ex-

tracts, requires the rior written consent of Reha & Medi Hoffmann GmbH.

1.2 Disclaimer

Understanding, observing and com lying with these instructions for use is absolutely es-

sential for atient safety and the safety of users as well as the trouble-free o eration of the

roducts of Reha & Medi Hoffmann GmbH. Reha & Medi Hoffmann GmbH does not assume

any warranty or liability for direct or indirect damage resulting from unauthorised modica-

tions to the roduct or failure to observe these instructions for use.

The roducts of Reha & Medi Hoffmann GmbH may only be used in conjunction with equi -

ment o tions a roved by the manufacturer as s ecied in the instructions for use.

Any combination of the roduct with other roducts, in articular with medical roducts, as

well as any technical modication to the roduct is generally not ermitted. Exce tions re-

quire the written a roval of the manufacturer.

Des ite careful checking, errors in this document cannot be com letely ruled out. We reser-

ve the right to make technical or content-related changes at any time without rior notice.

Documents in rinted form are not subject to a change service.

1.3 Definition of groups of persons

For reasons of better readability, the simultaneous use of the language forms male, female

and diverse (m/f/d) is dis ensed with.

Manufacturer

determines all measures to ensure safe and ro er handling and use and is res onsible for

instructing the o erator in this res ect.

Operator

is any natural or legal erson res onsible for the o eration of the healthcare facility in which

Der Mobilizer Medior is used by its em loyees.

User

is medical and nursing staff who use the roduct for mobilisation after instruction by the

o erator. As well as maintenance ersonnel with basic training in mechanical and mecha-

tronic systems who are res onsible for troubleshooting. Users are able to recognise, assess

and, if ossible, avoid otential hazards during use.

Patient

is a

- erson undergoing medical treatment

- erson in care

- cared for mentally and / or hysically im aired erson.

medical professionals (staff)

These are, among others, doctors, nurses, caregivers, hysiothera ists / occu ational the-

ra ists. Trainee healthcare rofessionals must be su ervised during use in addition to in-

struction.

Lay people and third parties

Lay ersons are ersons instructed in cleaning work by healthcare rofessionals. Third ar-

ties" also includes, for exam le, relatives of the atient.

These instructions for use have been re ared for users and o erators!

Instructions for use Mobilizer Medior

2. description, purpose, definition

The Mobilizer Medior is a mobile, height-adjustable inclined board and enables standing

exercises. To extend the thera eutic benet, intermediate ositions, such as sitting and sit-

ting ositions, can be continuously adjusted between the horizontal and vertical ositions

by means of a hand control unit with an electric motor and battery o eration.

Mobilizer Medior is suitable for atients from 14 years of age with a body length of 146 to

200 cm and can be adjusted to the required height by means of the height-adjustable foot-

rest.

Mobilizer Medior enables stabilisation of the torso and legs as needed. The individually ad-

justable ositions su ort the atient's head control and arm function. The u right body

osition can ex and the atient's eld of vision and im rove their s atial erce tion. The

extensive osition adjustment allows Mobilizer Medior to be used for thera eutic ur oses

and can also be used as art of the administration of nutrition.

Mobilizer Medior is also innitely adjustable during treatment between the horizontal and

vertical ositions, as well as to all intermediate ositions. The leg section moves synchro-

nously with the backrest.

When the atient is in the su ine osition, the range of functions with all intermediate osi-

tions can be used. In rone osition, Mobilizer Medior may only be swivelled between hori-

zontal and vertical osition with the lying surface level.

The sitting/lying surface is mounted on a com act chassis with four swivelling and brakable

castors, one of which can additionally be xed in direction, thus ensuring safe straight run-

ning. The castors are o erated by means of central foot control.

On both sides of Mobilizer Medior are u holstered armrests that raise and lower synchro-

nously with the backrest. The armrests can be swivelled in any osition to ensure barrier-

free lateral transfer of the atient in any lying or sitting osition. The body contact surfaces

are added and limited with swivelling side bars in the elvic and leg area, as well as in the

u er body area.

The foot xation, leg xation, elvic xation and u er body restraint are individually adjus-

table and added.

The u holstery has a ressure-relieving effect in the seat and back area due to a viscoela-

stic com onent in the u holstery foam and contributes to decubitus ro hylaxis.

All u holstery arts and covers are removable without tools, can be cleaned with standard

household cleaning agents, are resistant to disinfectants and have an anti-microbial nish.

The frame is owder-coated to revent corrosion, can be cleaned with standard household

cleaning agents and is resistant to disinfectants. The Mobilizer Medior is reusable.

2.1 Indication

De ending on the severity of the res ective functional or structural damage, tting with a

Mobilizer Medior may be indicated:

Signicant im airment of standing and walking, for exam le:

• Com lete/incom lete hemi legia (hemi aresis) and, if necessary, with involvement of

the trunk muscles as a result of a brain disease (for exam le, stroke, brain tumour).

• Com lete/incom lete aralysis of the arms and legs (tetra legia/ aresis) and, if neces-

sary, with involvement of the trunk muscles as a result of a disease of the brain (for ex-

am le, multi le sclerosis, brain injury), the s inal cord (for exam le, oliomyelitis, ara-

legia due to trauma or tumour) or the eri heral nervous system/muscular diseases (for

exam le, Guillain-Barré syndrome, muscular dystro hies).

• Com lete/incom lete aralysis of the legs ( ara legia/ aresis) and, if necessary, with

involvement of the trunk musculature as a result of a disease of the s inal cord (for ex-

am le, ara legia in the case of traumatic/inammatory/tumorous thoracic and lumbar

marrow lesion) or disease of the eri heral nervous system/muscular diseases (for ex-

am le, olyneuro athy, muscular dystro hies).

• For assuming a standing osition, for exam le in re aration for gait training and/or for

achieving ositive effects of an u right body osition (for exam le with regard to circula-

tion regulation/bone metabolism/bowel eristalsis/urinary drainage and/or for reventing

ressure sores, thrombosis or joint contractures, romoting head control and arm func-

tion and im roving s atial erce tion), if the clinical icture and the s atial conditions

make it necessary for the assistant/carer to change the location of the aid within the

home.

2.2 Contraindication

Selected contraindications to the use of Mobilizer Medior as a standing aid:

• Non-stabilised fractures, acute hase of a ara legic injury

• Sym toms of the failure of autonomous vascular regulation also in other neurological

and/or internal diseases.

• Cardiac emergency - acute, severe im airment of cardiovascular function.

• Surgical wounds - Patients with fresh wounds after surgical rocedures, such as a ster-

notomy after cardiac surgery, after lastic surgery to cover sacral or leg decubiti, should

not be raised, or only after a doctor's orders.

• The atient's body weight must not exceed 250 kg.

The Mobilizer Medior must not be used if a atient has failed the examination of a health-

care rofessional.

3. Permissible operating conditions/place of use

The Mobilizer Medior is intended for indoor use. If it is necessary to negotiate ste s or

thresholds, these must be slo ed or a ram must be created. The ram s or an inclined

lane may have a maximum gradient of seven degrees. The o erating tem erature range is

+5°C to +40°C.

Instructions for use Mobilizer Medior

. Dimensions

All dimensions in millimetres

Fig. 2: Mobilizer Medior in upright

position with vibration module

ATTENTION!

The osition adjustments may only be made on a horizontal surface. Use in o-

tentially ex losive atmos heres is not ermitted.

Fig. : Mobilizer Medior in lying position

Fig. 4: Mobilizer Medior in

sitting position

Instructions for use Mobilizer Medior

5. Safety instructions

5.1 Explanation of symbols and notes

For the safety of atients, for ersonal safety as well as to avoid damage to ro erty, the

meaning of the following symbol and note ex lanations must be observed. These are divi-

ded into hazard levels. If several degrees of severity occur, the warning for the highest level

is always used.

Safety and warning notices on the Mobilizer Medior

Safety and warning notices in the form of ictograms and stickers are attached to Mobilizer

Medior and to any equi ment su lied with it. These must not be changed or removed.

Defective or damaged notices must be re laced immediately. The manufacturer must be

contacted for this ur ose.

5.2 Basic safety information

The Mobilizer Medior is designed and manufactured in accordance with the state of the art

and its recognised safety rules. Nevertheless, risks of injury to staff, atients and third ar-

ties or damage to the Mobilizer Medior or other ro erty cannot be excluded if the Mobilizer

Medior:

• is not used according to the intended use,

• is o erated in a technically unsound condition or

• is o erated by untrained or uninstructed ersonnel.

ATTENTION!

Indicates a hazard. Failure to observe and avoid the situation may result in injury.

ATTENTION!

All safety instructions and warnings as well as the recommendations for action

in these instructions for use must be read! These must be followed without fail!

Failure to do so may result in ersonal injury and/or damage to or malfunction

of the Mobilizer Medior!

Pictogramm Meaning

Follow the instructions for use! Instructions for the safe use of Mobilizer

Medior are included and must be followed.

250 kg Observe the maximum atient weight! Non-observance can lead to inju-

ry to atients, medical staff and third arties or to damage to ro erty.

Occupational safety in general

ATTENTION!

General and national accident revention regulations must be observed. The

o erating ersonnel must be instructed accordingly. Safety and warning notices

on the Mobilizer Medior must not be changed or removed. Damaged notices

must be re laced immediately and can be obtained from the manufacturer.

Qualification of the staff

ATTENTION!

Only demonstrably instructed users are allowed to use the Mobilizer Medior

• a ly,

• clean,

• maintain and service as a recaution.

Commissioning

ATTENTION!

Before the Mobilizer Medior is ut into o eration, the medical staff must be in-

structed in its use by means of the instructions for use. The otential hazards

that may occur des ite ro er o eration of Mobilizer Medior must be ointed

out in detail.

Mobilizer Medior may only be o erated in accordance with its intended use and

only within its erformance limits.

In the event of malfunctions or defects that could im air safety, the Mobilizer

Medior must be taken out of o eration immediately and the fault must be recti-

ed immediately. To do this, contact authorised technicians or the manufacturer.

Never use Mobilizer Medior with defective technical safety devices.

Before utting the Mobilizer Medior and its accessories into o eration, a visual

ins ection must be carried out. For this ur ose, all cables must be checked for

external damage, connecting elements for tightness and the resence of the

rotective measures.

Instructions for use Mobilizer Medior

5.3 Operational capability

Before and during the use of Mobilizer Medior and its accessories, further instructions listed

below must be observed.:

• It must be ensured that the adjustment rocesses take lace without collision, continuously

and almost noiselessly.

• The function of the braking system must be checked according to item "13 Driving and bra-

king"..

• Com liance with hygiene requirements must be ensured. The ads must be checked for

damage that could affect their disinfectability..

• Make sure that the connecting and fastening elements function correctly..

• The smooth functioning of all o erating elements must be checked.

• The a liance may only be o erated by ersons who are familiar with these o erating in-

structions. These instructions must be ke t accessible to all o erators. If they are lost, they

must be obtained from the manufacturer.

• Before each transfer and when the atient sits down or stands u , the arking brake must

be activated to revent the Mobilizer Medior from rolling away unintentionally.

• The o erator must ensure that the erson on the Mobilizer Medior is suitably secured

against falling out.

• The o erator must ensure that no one can mani ulate the Mobilizer Medior or be injured by

moving arts during adjustment. The atient's arms should be in the atient's la or on the

armrests. The feet shall be laced securely on the footrest or on the oor.

• Avoid direct and rolonged skin contact with Mobilizer Medior for more than 1 hour by using

a suitable ad.

• The Mobilizer Medior and its individual com onents are sometimes subjected to high stres-

ses over the course of their useful life or in the event of im ro er handling. Any kind of

cracks or scratches can be indications that the com onent in question will suddenly fail,

which can lead to accidents with a risk of injury.

• Rattling noises or wobbling are an indication of defects!

• Technical modications are not ermitted. Only original arts from the manufacturer may be

used for re airs. A combination with other medical devices may only be carried out after

written a roval by all manufacturers or distributors involved.

• Re airs, maintenance and adjustment work may only be carried out by ersons who have

sufcient s ecialist knowledge. The EU Medical Device Regulation (MDR 2017/745) must be

observed.

• Regular roduct maintenance of Mobilizer Medior is recommended in order to reserve its

value.

• The linear actuators and the su ly cables must be free of external damage.

• Only the batteries intended for this ur ose may be used to o erate Mobilizer Medior!

5. Products with battery

Products with rechargeable batteries may only be o erated with the rechargeable batteries

su lied or other rechargeable batteries a roved by the manufacturer. The rechargeable bat-

teries may only be charged in the charging station rovided, including the mains ada ter.

Batteries

These are 24 V rechargeable batteries. Contact between the two contacts is almost im os-

sible due to the design. Do not touch the contacts, otherwise there is a risk of re or electric

shock. As a recaution, avoid wearing metallic jewellery, as touching the electrical contacts

can cause a short circuit in the battery and thus ose a risk of ex losion.

charging station

The external charging station for the batteries must be o erated se arately and must not be

connected to the roduct for mains o eration. The charging station may only be o erated out-

side the atient environment. The charging station and the mains ada ter with su ly cable

must be checked for external damage. The mains ada ter is subject to the relevant regulations

for mains- owered devices.

5.5 Product life

The ex ected technical roduct life is set by the manufacturer at 10 years, rovided the

intended use and safety instructions are observed. Daily use rovides for 10 a lications

on 5 consecutive days followed by 2 rest days. It is recommended to limit one a lication

to 15 minutes.

ATTENTION!

Risk of destruction of the electric motors and re hazard when using unauthori-

sed batteries and charging stations! Recharging of batteries is only ermitted

with the charging station su lied by the manufacturer.

Gebrauchsanleitung Mobilizer Medior

6. Height adjustment

Mobilizer Medior is equi ed with a height ad-

justment that works inde endently of the lying

or sitting osition. It is o erated by means of

a hand switch (see Fig. 7).

Fig. 5: Height adjustment

7. Backrest adjustment

By tilting the backrest, Mobilizer Medior can

be adjusted from a at lying surface to a sitting

osition. Synchronously with the inclination of

the backrest, the leg rest is also lowered or rai-

sed. The o eration is done by means of a

hand switch (see g. 7).

The Mobilizer Medior is characterised by a re-

duction of the shear forces that are otherwise

common when adjusting the backrest. De en-

ding on the inclination of the backrest, the

seat cushion is shifted in the longitudinal di-

rection and adjusted (tilted) at the front. This

gives the atient a stable sitting osition wi-

thout shifting during sitting u .

Fig. 6: Backrest adjustment

8. Hand control

The tilt of the backrest and seat, as well as the adjustment of the seat height, is carried out

by means of electric motors. O eration is via a hand control (see Fig. 6). The hand control

has six function keys in the u er three rows of keys (framed in black) and four rogramme

keys with reset ositions in the lower two rows of keys (framed in white). The status LED

in the u er left area of the hand control indicates the battery charge status and only lights

u when the Mobilizer Medior is in o eration (see 10. Changing the battery).

8.1 Function keys

The function keys offer the ossibility to adjust the height adjustment, the backrest tilt and

the seat tilt se arately. However, for safety reasons, certain areas are blocked.

For exam le, the forward tilt is only ermitted in the highest osition of the height adjust-

ment. When using the rogramme buttons, such conditions are automatically created.

1 - Raise height adjustment

2 - Lower height adjustment

3 - Raise backrest

4 - Lowering the backrest

5 - Seat tilt forward

6 - Seat inclination to the rear

8.2 Programme buttons

Predened movement cycles are assigned to the

rogramme buttons. To set the desired end osi-

tion, the res ective button must be ke t ressed

until the corres onding osition is reached. If the

button is released before the end osition is rea-

ched, Mobilizer Medior sto s. Pressing it again

resumes the movement cycle.

7 - Position standing bed

8 - Chair osition

9 - Position couch

10 - Shock osition

Abb. 7: Handschalter

Status-LED

9. Main switch

Behind the backrest below the battery is the red

main switch (see Fig. 8), which is used to switch

off all drives of the Mobilizer Medior by ushing

in the switch button. Turning the red control

knob clockwise releases it again.

Fig. 8: Main switch

10. Transfer

Patients can be transferred sideways into and out of Mobilizer Medior in a sitting or lying

osition. Patients whose mobility allows it are also able to get out forwards or sit in the

standing-u osition. In rinci le, Mobilizer Medior must be braked every time the atient

is transferred or sits in or gets out of the chair.

10.1 Horizontal transfer

Before transferring atients lying down, lower the backrest to the at lying osition and the

footrest to the lowest ste . Patients are to be ositioned so that their greater trochanter

(large rolling mound) is ositioned above the rear end of the seat cushion. In this osition,

the to of the atient's head must not rotrude above the head cushion. Moving the atient

towards the head end or foot end is not ermitted (see Fig. 9 and Fig. 10). The backrest

must be raised to achieve a semi-sitting osition and the footrest adjusted to the atient's

lower leg length according to cha ter 12.

ATTENTION!

In the lying osition, the atient's body weight must be evenly distributed. The

atient's centre of gravity must be on the seat cushion (a lies es ecially to

am utees). Lifting the legs may cause the Mobilizer Medior to ti over.

Fig. 9: Permissible patient positioning Fig. 10: Inadmissible patient positioning

Instructions for use Mobilizer Medior

ATTENTION!

Mobilizer Medior is not suitable as a climbing aid, nor is it ermitted to sit down

on the backrest or foot end. An im ermissible load can cause the Mobilizer

Medior to ti over.

10.2 Sitting transfer

Alternatively, the armrests can be swivelled u wards to allow comfortable lateral transfers

in sitting ositions. If atients are transferred to Mobilizer Medior in a sitting osition, they

should only be ositioned on the seat surface so that the lower art of the back rests

against the backrest and the atient can assume an u right sitting osition.

To get out forward, the seat of Mobilizer Medior is tilted forward as far as it will go and the

footrest is stowed under the calf ad. In this osition, an attendant can hel the atient out

of Mobilizer Medior with minimal effort while observing kinaesthetic rinci les.

Fig. 11: Armrest swivelled upwards

Fig. 12: Locking the armrest in

place

11. Armrests

The armrests rovide su ort for the atient without

limiting the seat width. They lower automatically to

the level of the seat cushion when adjusted to the

couch, facilitating the rone lateral transfer of ati-

ents. For seated transfer or lateral sitting, it is ossi-

ble to swivel the armrests u wards individually (see

Fig. 11).

Locking the armrests

According to the sco e of equi ment, the armrests

can be locked in any osition by means of a locking

lever (see Fig. 12).

Instructions for use Mobilizer Medior

ATTENTION!

The foot ste may only be folded in in the extended osition to avoid damage

to the calf ad.

Fig. 1 : Positioning the feet on

the foot step

12. Footstep

Positioning

The atient's feet must be ositioned centrally aral-

lel on the foot ste (see g. 10). The atient's feet

must not rotrude beyond the footrest. The symme-

trical arrangement of the feet on the foot ste ensu-

res o timal function and revents the risk of ti ing

over due to uneven load distribution. For a lying

transfer or if the foot ste is not needed, it can be fol-

ded under the calf ad. To do this, lift the calf ad,

fold in the fully extended foot ste and then ut the

calf ad down again.

Fig. 14: Electric footrest adjustment

electric footrest adjustment

The footrest can be continuously adjusted to the

length of the atient's lower leg. To do this, ress the

buttons on both sides underneath the seat cushion

(see Fig. 14) to raise or lower the footrest.

Fig. 15: Brake lever

13. Driving and braking

With the foot control lever at the rear of the

frame, both the directional and the total locking

of the castors are o erated centrally. For driving

straight ahead, the directional castor at the front

right can be locked by lifting the central brake

lever.

Pushing down the central brake lever (Fig. 15)

locks the rear brake rollers and the directional

roller (all-wheel brake). The central, horizontal

osition of the central brake lever causes free-

wheeling and free ivoting of all wheels.

ATTENTION!

To revent unintentional rolling away, the arked Mobilizer Medior must al-

ways be braked.

1 . CPR function

The foot switches for the CPR function (see Fig.

16) are installed on both sides centrally in the

lower art of the chassis on the Mobilizer Medior

and can be triggered from any osition. When the

CPR switch is actuated, the level, horizontal lying

surface is set.

Fig. 16: CPR switch

ATTENTION!

The angle of the seat to the backrest is dis layed, regardless of the inclination

of the seat.

Fig. 17: Angle display

15. Angle display

The angle indicator is located on both sides of

the Mobilizer Medior under its seat (see Fig. 17).

The reading oint of the angle at the recess of the

cover late is marked with a dot.

16. Battery change

All functions of Mobilizer Medior are owered by an electric

motor in battery mode. An LED indicator light on the battery

holder (see Fig. 18) shows the current charge status:

• green: sufcient charge - battery full

• yellow, a short bee sounds when a button is ressed:

charge is running low, recharge the battery.

• red, a re eating bee sounds: low charge - be sure to

charge the battery before using Mobilizer Medior.

Fig. 18: Battery control

light

ATTENTION!

The weight of the battery is u to 5 kg, de ending on the ty e of battery. When

removing the battery, make sure that it does not fall down when detaching it.

Fig. 19: Removing the batte-

Fig. 20: Inserting the bat-

tery

Fig. 21: Charging station with

wall bracket

The battery is freely accessible behind the backrest. To change the batteries, the backrest

should be moved to a vertical osition and the arking brake a lied. To release the battery,

ull it to the left with a slight jerk and then lift it off the backrest (see Fig. 19). To insert the

charged battery, roceed in reverse order. To charge the battery, insert it into the charging

station. The battery is inserted into the charging station in the same way as on the battery

holder on the Mobilizer Medior (see Fig. 20). Please also observe the general safety instruc-

tions (cha ter 5). The charging station should referably be mounted vertically on a wall

(see Fig. 21) so that the battery is inserted into the charging station from above for charging.

INFORMATION

De ending on the battery ty e, the battery must be re laced regularly. If

the battery erformance dro s noticeably, contact your customer advisor

or the manufacturer.

Instructions for use Mobilizer Medior

Table of contents

Other rehamedi Medical Equipment manuals

rehamedi

rehamedi Ottfried User manual

rehamedi

rehamedi Curalizer Arne User manual

rehamedi

rehamedi Norbert User manual

Popular Medical Equipment manuals by other brands

Haag-Streit

Haag-Streit BX 900 Instructions for use

ZacUrate

ZacUrate 430P user manual

HEINE

HEINE iC1 quick start guide

Omron

Omron Large Cuff manual

Rossmax

Rossmax SB100 user manual

NeurOptics

NeurOptics PLR-4000 Instructions for use

Nipro

Nipro PHOENIX ONE Operator's manual

Siemens

Siemens MAMMOMAT 1000 Nova Maintenance instructions

EMS

EMS COMBINATION 850 manual

Heyer

Heyer Narkomat + Operator's manual

NeoMedLight

NeoMedLight BiliCocoon Instructions for use

Konica Minolta

Konica Minolta REGIUS CS-2 brochure

TransMedics

TransMedics Organ Care System Technical user guide

Basic American

Basic American ZENITH Series Instructions for use

Masimo

Masimo O3 Regional Oximeter Operator's manual

Tecno-gaz

Tecno-gaz KYRI DSS instruction manual

Reinecker

Reinecker Videomatic user manual

Jumper

Jumper JPD-500G Instructions for use

rehamedi Medior User manual

Popular Medical Equipment manuals by other brands