Drive Medical Padded Swivel Seat Cushion Manuel utilisateur

Marque: Drive Medical

Modèle: Padded Swivel Seat Cushion

Taper: Manuel utilisateur

Operating Manual

Item # RTLAGF-1000

Consult instructions for use

Table of Contents

Introduction ................................................................................................................................. 1

Indications for Use ...................................................................................................................... 1

Safety Warning ........................................................................................................................... 2

Contraindications ........................................................................................................................ 2

Warnings .................................................................................................................................... 2

Precautions ................................................................................................................................. 3

Adverse Reactions ...................................................................................................................... 4

Symbol and Title ..................................................................................................................... 4, 5

Environmental Condition for Transport and Storage .................................................................... 6

Electromagnetic Compatibility ................................................................................................. 6, 7

How the Device Works .............................................................................................................. 11

Setup ........................................................................................................................................ 12

Operating Instruction ................................................................................................................. 13

Performance Specifications ...................................................................................................... 18

Cleaning and Maintenance ....................................................................................................... 18

Trouble Shooting ...................................................................................................................... 18

Recommended Use Positions ................................................................................................... 19

Warranty ................................................................................................................................... 20

Contact Information................................................................................................................... 20

Introduction

RTLAGF-1000 delivers electric pulses and heat generated to the user’s body areas

such as legs and feet through the electrodes. The portable and compact device has

multiple modes of different pulse frequencies, covering Transcutaneous Electrical Nerve

Stimulation (TENS) and Electrical Muscle Stimulation (EMS). It includes operating

elements of ON/OFF button, intensity increase button, intensity decrease button, mode

button, timer button, heat/temperature button, and could be attached and detached to

electrodes through the magnetic connectors.

Indications for Use:

TENS (Modes 1, 2, 4, 5, 6, 8)

To be used for temporary relief of pain associated with sore and aching muscles in the

shoulders, waist, back, arms and legs, due to strain from exercise or normal household

and work activities.

It is also intended for symptomatic relief and management of chronic, intractable pain

and discomfort associated with arthritis.

EMS (Modes 1, 3, 7)

To stimulate healthy muscles to improve and facilitate muscle performance. To be used

for the improvement of muscle tone and firmness and for strengthening muscles in the

arms, abdomen, legs, and buttocks. Not intended for use in any therapy or for the

treatment of any medical conditions or diseases.

It is also intended to temporarily increase local blood circulation in the healthy muscles

of lower extremities.

Heating Mode

Temporary relief of minor aches and pains.

Safety Warning

Caution, consult accompanying documents

Contraindications:

w Do not use this device on persons who have a cardiac pacemaker, implanted

defibrillator, or other implanted metallic or electronic device because this may cause

electric shock, burns, electrical interference or death.

w Do not use this device on persons whose pain syndromes are undiagnosed.

Warnings:

w WARNING: Use carefully. May cause serious burns. Do not use over sensitive skin

areas or in the presence of poor circulation. The unattended use of this device by

children or incapacitated persons may be dangerous. To reduce the risk of burns,

electric shock and fire this device must be used in accordance with the instructions.

w Do not crush the device or its electrode, and avoid sharp folds.

w Carefully examine the device and its electrodes, do not use if they show any sign of

deterioration.

w Do not tamper with this device and its electrodes in any way. There are no user

serviceable parts. If for any reason they do not function satisfactorily, return to the

authorized service dealer where purchased from.

w The long-term effects of chronic electrical stimulation are unknown.

w Stimulation should not be applied over the carotid sinus nerves, particularly in persons

with a known sensitivity to the carotid sinus reflex. Carotid sinus is located on both sides

of the neck (Refer to Page 20 for details).

w Stimulation should not be applied over the front of neck or mouth. Severe spasm of

the laryngeal and pharyngeal muscles may occur and the contractions may be strong

enough to close the airway or cause difficulty in breathing. Stimulation over the neck

can also cause adverse effects on heart rhythm or blood pressure.

w Do not apply stimulation across the patient’s chest because the introduction of

electrical current into the chest may cause rhythm disturbances to the patient’s heart,

which could be lethal.

w Since the effects of stimulation of the brain are unknown, stimulation should not be

applied across the head and electrodes should not be placed on opposite sides of head.

w Stimulation should not be applied over swollen, infected, or inflamed areas or skin

eruptions, e.g., phlebitis, thrombophlebitis, varicose veins, etc.

w Stimulation should not be applied over, or in proximity to, cancerous lesions.

Precautions:

w Safety of stimulation use during pregnancy has not been established. Consult with

your physician before use during pregnancy.

w Caution should be used for persons with suspected or diagnosed heart problems.

w Caution should be used for persons with suspected or diagnosed epilepsy.

w Caution should be used if you have any of the following:

• If you have a tendency to bleed internally following an injury.

• If you recently had surgery, or have ever had surgery on your back.

• If areas of skin lack normal sensations, such as skin that is numb.

w Consult with your physician before use over the menstrual uterus.

w You may experience skin irritation or hypersensitivity due to the electrical stimulation

or electrical conductive medium. The irritation can usually be reduced by using an

alternate conductive medium, or alternate electrode placement.

w Do not use this device while driving, operating machinery, or during any activity in

which involuntary muscle contractions may put the user at undue risk of injury.

w Keep this device out of reach of children.

w Do not use this device while sleeping.

w Do not use this device in high humidity areas such as, a bathroom.

w Stop using this device at once if you feel discomfort, dizziness or nausea, and consult

your physician immediately.

w Do not attempt to move the electrodes while the device is operating.

w Do not apply stimulation of this device in the following conditions:

● Across the chest because the introduction of electrical current into the chest may

cause

rhythm disturbances to the heart, which could be lethal.

● Over open wounds or rashes, or over swollen, red, infected, or inflamed areas or

skin

eruptions (e.g., phlebitis, thrombophlebitis, varicose veins).

● In the presence of electronic monitoring equipment (e.g., cardiac monitors, ECG

alarms).

● On children or incapacitated persons.

w Be aware of the following:

● Consult with your physician before using this device.

● This device is not effective for pain associated with Central Pain Syndromes, such

headaches.

● This device is not a substitute for pain medications and other pain management

therapies;

● This device is a symptomatic treatment and, as such, suppresses the sensation of

pain

that would otherwise serve as a protective mechanism.

● Stop using the device if the device does not provide pain relief.

● Use this device only with the electrodes, and accessories recommended for use by

the

manufacturer.

w Store the device away from high-temperature and direct-sunlight. Storage outside of

stated storage temperature may result in measurement error or device malfunction.

w Do not share the use of the electrodes with others; electrodes are intended for single

person use.

w Do not use the device while it’s charging.

w This device contains a lithium battery. If overheating of the device occurred during the

charging, stop the charging or operation immediately and contact customer support.

w Dispose of this battery-containing device according to the local, state, or federal laws.

w Skin burns may occur, and check the skin under the electrode periodically.

Adverse Reactions

w You may experience skin irritation and burns beneath the stimulation electrodes

applied to the skin; check skin under electrodes frequently.

w You should stop using the device and should consult with your physicians if you

experience adverse reactions from the device.

Symbol and Title

Information essential for proper use shall be indicated by using the corresponding

symbols. The following symbols may be seen on the device and labeling.

Symbol

Title

Consult instructions for use

Caution, consult accompanying

documents

Use by date

Date of manufacture

Batch code

Catalog number

Serial number

Manufacturer

Temperature limitation

Humidity limitation

Non-sterile

MR Unsafe - keep away from magnetic

resonance imaging (MRI) equipment

Fragile, handle with care

Keep away from rain

Product packaging is able to be recycled

Environmental Condition for Transport and Storage

- Normal working ambient temperature: 10~40°C

- Normal working ambient humidity: 30~85%

- Store and transport ambient temperature: -10 ~50°C

- Store and transport ambient humidity: 30~90%

Fragile; handle with care

Keep away from rain

Product packaging is able to be recycled

Non-sterile

Electromagnetic Compatibility

1) This product needs special precautions regarding electromagnetic compatibility

(EMC) and needs to be installed and put into service according to the EMC information

provided, and this unit can be affected by portable and mobile radio frequency (RF)

communications equipment.

2) Do not use a mobile phone or other devices that emit electromagnetic fields, near the

unit. This may result in incorrect operation of the unit.

3) Caution: This unit has been thoroughly tested and inspected to ensure proper

performance and operation!

4) Caution: This machine should not be used adjacent to or stacked with other

equipment and that if adjacent or stacked use is necessary, this machine should be

observed to verify normal operation in the configuration in which it will be used.

Guidance and manufacture’s declaration – electromagnetic emission

The device is intended for use in the electromagnetic environment specified below. The

customer of the user of the device should ensure that it is used in such an environment.

Emission test

Compliance

Electromagnetic environment – guidance

RF emissions

CISPR 11

Group 1

The device uses RF energy only for its internal

function. Therefore, its RF emissions are very

low and are not likely to cause any interference

in nearby electronic equipment.

RF emission

CISPR 11

Class B

The device is suitable for use in all

establishments, including domestic

establishments and those directly connected to

the public low-voltage power supply network

that supplies buildings used for domestic

purposes.

Harmonic

emissions

IEC 61000-3-2

Class A

Voltage

fluctuations/ flicker

emissions

IEC 61000-3-3

Complies

Guidance and manufacture’s declaration – electromagnetic immunity

The device is intended for use in the electromagnetic environment specified below. The

customer or the user of the device should ensure that it is used in such an environment.

Immunity test

IEC 60601 test

level

Compliance

level

Electromagnetic

environment - guidance

Electrostatic

discharge (ESD)

IEC 61000-4-2

±6 kV contact

±8 kV air

±6 kV contact

±8 kV air

Floors should be wood,

concrete or ceramic tile. If

floor are covered with

synthetic material, the

relative humidity should be

at least 30%.

Electrical fast

transient/burst

IEC 61000-4-4

±2 kV for power

supply lines

±1 kV for

input/output lines

±2kV for power

supply lines

Mains power quality should

be that of a typical

commercial or hospital

environment.

Surge

IEC 61000-4-5

± 1 kV line(s) to

line(s)

± 2 kV line(s) to

earth

±1 kV differential

mode

Mains power quality should

be that of a typical

commercial or hospital

environment.

Voltage dips,

short

interruptions and

voltage variations

on power supply

input lines

IEC 61000-4-11

<5% U

(>95% dip in U

)

for 0.5 cycle

40% U

(60% dip in U

)

for 5 cycles

<5% U

(>95% dip in U

)

for 0.5 cycle

40% U

(60% dip in U

)

for 5 cycles

Mains power quality should

be that of a typical

commercial or hospital

environment. If the user of

the device requires

continued operation during

power mains interruptions, it

is recommended that the

70% U

(30% dip in U

)

for 25 cycles

<5% U

(>95% dip in U

)

for 5 sec

70% U

(30% dip in U

)

for 25 cycles

<5% U

(>95% dip in U

)

for 5 sec

device be powered from an

uninterruptible power supply

or a battery.

Power frequency

(50Hz/60Hz)

magnetic field

IEC 61000-4-8

3 A/m

Power frequency magnetic

fields should be at levels

characteristic of a typical

location in a typical

commercial or hospital

environment.

NOTE U

is the a.c. mains voltage prior to application of the test level.

Guidance and manufacture’s declaration – electromagnetic immunity

The device is intended for use in the electromagnetic environment specified below. The

customer or the user of the device should ensure that it is used in such an environment.

Immunity

test

IEC 60601 test

level

Complianc

e level

Electromagnetic environment - guidance

Conducted

IEC 61000-

4-6

3 V

rms

150 kHz to 80

MHz

3 Vrms

Portable and mobile RF communications

equipment should be used no closer to any

part of the device, including cables, than the

recommended separation distance

calculated from the equation applicable to

the frequency of the transmitter.

Recommended separation distance

Where P is the maximum output power

rating of the transmitter in watts (W)

according to the transmitter manufacturer

and d is the recommended separation

distance in meters (m).

Field strengths from fixed RF transmitters,

as determined by an electromagnetic site

survey,

should be less than the compliance

level in each frequency range.

Interference may occur in the vicinity of

equipment marked with the following

symbol:

Radiated

IEC 61000-

4-3

3 V/m

80 MHz to 2.5

GHz

3 V/m

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

NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation

is affected by absorption and reflection from structures, objects and people.

a Field strengths from fixed transmitters, such as base stations for radio

(cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio

broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess

the electromagnetic environment due to fixed RF transmitters, an electromagnetic site

survey should be considered. If the measured field strength in the location in which the

device is used exceeds the applicable RF compliance level above, the device should be

observed to verify normal operation. If abnormal performance is observed, additional

measures may be necessary, such as re-orienting or relocating the device.

b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3

V/m.

Recommended separation distances between portable and mobile RF

communications equipment and the device.

The device is intended for use in an electromagnetic environment in which radiated RF

disturbances are controlled. The customer or the user of the device can help prevent

electromagnetic interference by maintaining a minimum distance between portable and

mobile RF communications equipment (transmitters) and the device as recommended

below, according to the maximum output power of the communications equipment.

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 2.5 GHz

0.01

0.12

0.23

0.1

0.38

0.73

1.2

2.3

3.8

7.3

100

For transmitters rated at a maximum output power not listed above, the recommended

separation distance d in meters (m) can be estimated using the equation applicable to the

frequency of the transmitter, where P is the maximum output power rating of the transmitter

in watts (W) according to the transmitter manufacturer.

NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range

applies.

NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is

affected by absorption and reflection from structures, objects and people.

How the Device Works

The device has multiple modes, covering TENS and EMS. If you are using the device

for the first time, it is recommended that you start with the default Mode 1, which

combines different pulse frequencies. Some modes are particularly effective for certain

users, but you may need to select both the mode and the electrode position that are the

best for you. You may need to try a few positions and modes before finding the one that

suits you the best. The best choice of modes and positions may vary from one user to

another, in spite of having the same type of symptom.

Program

Pulse frequency (Hz)

Mode 1: TENS and EMS

Combination of the following Mode 2-7

Mode 2: TENS

Mode 3: EMS

12.5-55.6

Mode 4: TENS

1.2

Mode 5: TENS

100 (On for 10 seconds and off for 2.5 seconds)

Mode 6: TENS

100 (On for 20 seconds and off for 1 seconds)

Mode 7: EMS

Mode 8: TENS

160

Setup

Unpack the box of the product, and take the product and accessories out. The

accessories may include electrodes, USB cable and AC adapter. The USB cable could

be used to charge the control unit.

Operating Instruction

The following steps are used to guide the device operation, and the details about each

step are listed in the following table.

Step – Check the battery in the control unit

Battery recharging

The control unit comes with a built-in rechargeable

battery, and could be used as received. If the

battery icon on the turned-on control unit keeps

flashing, it means the battery is running out.

Charge the control unit with the enclosed USB

cable and AC adapter. USB cable could connect

to any certified adapters. The battery icon flashes

during charging, and becomes solid when the

control unit is charged fully.

Step - Install the electrode onto the control

unit

Electrode installment

Place the enclosed electrode onto the back side of

the control unit using the magnetic snaps. Match

up the silver magnetic snaps on the electrode pad

with the silver magnetic snaps on the control unit,

follow the same steps for the gold. This should be

done before applying the device onto the skin of

treatment areas.

Step - Place the electrode-installed device

on the stimulation-needed body area

Place the device on the body area

Place the pad-installed device onto the treatment

area (such as the shoulder). Press down firmly

and ensure a firm contact with the body skin.

Note: Keep the skin clean before placing the

device.

Step - Press the “ON/OFF” to turn on the

power

Holding the On/Off button could turn on the

device, indicated by the lit-up display on the front

of device. You could press and release the On/Off

button to lock/unlock the buttons on the device

front. When the buttons are locked, you could not

operate them. However, you still could turn the

device off by holding the On/Off button.

Step - Select one of the stimulation modes

There are totally 8 preset stimulation modes.

Press the “M” button to select a desired pulse

mode. The mode selected will be shown on the

display.

Step - Choose the stimulation time

The default timer is 30 min, and pressing the “T”

button could select a desired timer (30, 40, 50, 60,

10, and 20 min). The timer selected will be shown

on the display.

Step - Adjust the stimulation intensity

Pressing the “+” button could increase the

intensity, while pressing the “-” button could

decrease the intensity. The intensity change will

be reflected on the display.

Note: With the increase of intensity (total of 20

levels), you may experience sensations like

tingling, vibration, pain, etc. Therefore, gradually

increase the intensity, and stop increasing when a

comfortable level is reached.

Step – Use heat/temperature on the device

Press the “Heat +/-” button for the first time to turn

on the heat Level 1 of up to 104

F, for the second

time to adjust to Level 2 of up to 109.4

F and for

the third time to turn off the heat. The heat will be

reflected on the display.

Note: The device is used for the electrical

stimulation or heat; consult with your physician

before using electrical stimulation and heat

simultaneously.

Step - Hold the “ON/OFF” again to turn off

the power after done

When the countdown timer is up, the device will

turn off automatically. The device could be also

turned off by holding the On/Off button, indicated

by the display light off.

Remote Operation

As shown above, the Electronic Pulse Stimulator could be operated independently by

pressing its buttons (ON/OFF button, intensity increase/decrease buttons, mode/timer

selection buttons and heat/temperature button). As the optional accessory, the remote

control could provide a secondary operation way to wirelessly control the functions

mentioned above. At any time, you could switch to manually operate the device itself by

pressing its buttons to deal with any issues that may arise.

1. Follow the above instruction to install the electrode onto the device, place on the

body area, and turn on the device.

2. Recharge the battery of the remote if needed by inserting the USB cable to the

top of the remote, which could connect to the adapter included or any certified

adapters.

3. Switch the ON/OFF button to turn on the remote, indicated by its first LCD

display on.

Note: You could press and release the lock/unlock button on the remote to

lock/unlock the buttons on the remote and device. When the buttons are locked,

the lock icon on the remote appears, and you could not operate the buttons on

the remote and device. However, you still could turn the remote and device off by

switching the On/Off button.

4. Pressing and releasing the “+” button on the remote would increase the intensity

of the device, while pressing and releasing the “-” button on the remote would

decrease the intensity of the device. Each time when the intensity

increase/decrease once, the intensity bar on the remote will accordingly

increase/decrease once.

Note: With the increase of intensity (total of 20 levels), you may experience

sensations like tingling, vibration, pain, etc. Therefore, gradually increase the

intensity, and stop increasing when a comfortable level is reached.

5. Press and release the “HEAT” button on the remote for the first time to turn on

the heat Level 1 of up to 104

F, indicated by the first HEAT indicator flashing on

the LCD display; press and release the “HEAT” button for the second time to

adjust to Level 2 of up to 109.4

F, indicated by the second HEAT indicator

flashing on the LCD display; press and release the “HEAT” button for the third

time to turn off the heat, indicated by the HEAT indicator stop flashing.

6. There are total of 8 preset stimulation modes. Press and release the “M/T” button

on the remote to select a desired pulse mode, indicated by the flashing of the

selected mode on the LCD display.

7. The default timer is 30 min. Pressing and holding the “M/T” button could select a

desired timer in the order of 30, 40, 50, 60, 10, and 20 min, indicated on the LCD

display.

8. When the countdown timer is up, the remote and device will turn off

automatically. The remote and device could be also turned off by switching the

On/Off button on the remote, indicated by the LCD display off.

Note: When the battery of the remote is running low, its battery icon will flash,

meaning it is time to recharge the battery.

If using the device for the first time, you may start from the default Mode 1, which

combines the different frequencies. If you expect to use the specific TENS or EMS

mode, please refer to the following for details.

Use as TENS

The Electronic Pulse Stimulator with Heat includes the following TENS frequencies,

69Hz (Mode 2), 1.2 Hz (Mode 4), 100Hz (Modes 5 and 6), and 160Hz (Modes 8). The

device could be placed directly on the treatment site where you are experiencing pain

(such as pain associated with sore and aching muscles and pain associated with

arthritis). For example, if the treatment site is on the leg, place the TENS device above

the pain site, and select one of the modes mentioned.

Arthritis involves inflammation on joints of the body, usually producing pain and

stiffness. The electrode is placed on or near the area of the arthritis pain. The TENS

mode of the device generates electrical pulses that are sent via the electrode for pain

relief.

Use as EMS

The Electronic Pulse Stimulator also includes the EMS frequency, 12.5-55.6Hz (Mode

3) and 20Hz (Mode 7). The device could be placed directly on the body area where you

are expecting the muscle firming and strengthening. For example, if the body area is the

arm, place the device on the arm site, and select Mode 3 or 7.

Also, the EMS mode could help temporarily increase local blood circulation in the

healthy muscles of lower extremities through the electrode pad which is positioned on

the lower extremity.

Recommended Practice for Both TENS and EMS:

• Duration suggested for each body area is 30 min and 2 times per day. Consult with

your physician for longer and more frequent uses.

• Start from the lowest intensity and gradually adjust the intensity to a comfortable

level at a scale from 1 to 20.

• Good skin care is important for a comfortable use of device. Be sure the treatment

site is clean of dirt and body lotion.

• Keeping the electrode in the storage bag after use will extend its lifespan. The

electrode pad is disposable and should be replaced when it loses the adhesiveness.

To purchase additional electrodes, please contact the seller.

As shown in the above device operation, there is one kind of electrode pad used with

the Pain Away Pro with Heat. The biocompatible electrode pad, consists of electrode

gel, conductive film, heating layer, backing material, and connectors.

In addition, it is worth mentioning the button-lock feature is very practical, which could

prevent any unintended operations during use. Pressing the On/Off button twice could

activate/deactivate the button-lock feature. This feature would not affect the safety or

effectiveness of the subject device, and the user could still turn off the device by holding

the On/Off button. After selecting the appropriate mode, intensity, and timer, the user

could activate the button-lock; when the timer is up, the device will turn off

automatically.

Electrodes with a shelf life of 2 years are intended for single person use, and could be

replaced. If the electrode no longer contacts well with your body skin, it is time to

replace it. If needed, you could use a damp and clean cloth to wipe electrodes between

uses. Please see the following for the Directions for Use, Removal and Storage of the

electrode used for both TENS and EMS.

Directions for Use

1. Clean skin thoroughly prior to each application of electrodes, which will not contact

well if any lotion, make-up, or dirt is left on the body skin.

2. Ensure the device is off before applying the electrode to it.

3. Apply the electrode-installed device firmly to the body skin.

Removal and Storage

1. Turn the device off before removing the electrode from the body skin.

2. Grab the edge of the electrode and remove from the body area.

3. When not in use and/or between each use, store the electrode in the re-sealable bag,

out of direct sunlight.

Heating Mode

In addition to the TENS and EMS modes described above, the device has an additional

mode of heat/temperature. When used in the heating function, the device will couple

with an electronically controlled electrode pad or garment to provide automatic thermal

heat to the skin with a range of 96.8 °F - 109.4 °F. This automatic thermal control

mechanism could also avoid skin from thermal injury. The device is used for the

electrical stimulation or heat; consult with your physician before using electrical

stimulation and heat simultaneously.

Performance Specifications

Power Source 3.7V Battery

Number of Output Modes 8 preset modes

Timer Range (minutes) 10-60

Dimensions (mm) [L x W x D] 89 x 77 x 18 mm

Waveform Biphasic

Shape Rectangular

Maximum Output Voltage 46V@500Ω

Maximum Output Current 92mA@500Ω

Maximum Pulse Duration 100µSec

Maximum Frequency 160Hz

Cleaning and Maintenance

Please use a wipe to clean the device first, and then use a dry cloth to wipe it again. The

electrodes coming with the device are disposable and should be replaced when they lose

their adhesiveness. Contact the seller for replacements. Replacement Electrodes, Item#

RTLAGF-1010, comes with 1 small and 1 large electrode.

Trouble Shooting

If your device is not operating properly, please check below for common problems and

suggested solutions. If the recommended action does not solve the problem, please contact the

seller.

Stimulation is weak or non-existent

• Be sure skin is clean and pads are firmly attached to skin.

• The battery is low and needs to be charged.

Devise does not turn on

• Check if battery is low and needs to be charged.

Electrodes are not sticky

• The pads will lose adhesiveness over use. Please contact the distributor or dealer

for replacements.

Skin turns red

• Stop to treat another area.

• If problem persists, contact your physician.

Wireless control not connected

• Restart the device and wireless controller to re-connect automatically.

• Switch to operate the device itself manually.

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Drive Medical Padded Swivel Seat Cushion Manuel utilisateur

Marque: Drive Medical

Modèle: Padded Swivel Seat Cushion

Taper: Manuel utilisateur

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