Instruction Manual

Treatment Table
3000.9xx

GA-A 176 / en / 2012-05 V6.0 / PDG 11-5360

 Important general notes and instructions for use
Make sure that this product is used only as intended and described in this instruction manual, by adequately
trained and qualified medical personnel, and that maintenance and repair are only carried out by authorized
experts.
Use the product only in the combinations and with the accessories and spare parts specified in this instruction
manual. Use other combinations, accessories and replacement parts only if they are expressly intended for
the planned application and if the performance characteristics and safety requirements are not impaired. Do
not alter the product.
Reprocess the products before each use and before return shipment as required by the instruction manual
to protect the patient, user and others.
Immediately upon receipt, check the product and its accessories for completeness and possible damage.
Should the shipment give right to complaints, please inform the manufacturer or supplier immediately.
Subject to technical changes!
Due to the continuous development of our products, the illustrations and technical data may deviate slightly.

Safety instructions and levels of danger

Symbol Level of danger
WARNING!
Failure to observe can result in death or serious injury.
CAUTION!
Failure to observe can result in slight injury or damage to the product.
IMPORTANT!
. Failure to observe can result in damage to the product or surroundings.
NOTE!
. Tips for optimum use and other useful information.

GERMANY USA UK
RICHARD WOLF GmbH RICHARD WOLF RICHARD WOLF UK Ltd.
75438 Knittlingen Medical Instruments Corporation Waterside Way
Pforzheimerstr. 32 353 Corporate Woods Parkway Wimbledon
Telephone: +49 70 43 35-0 Vernon Hills, Illinois 60061 SW17 0HB
Telefax: +49 70 43 35-300 Toll Free: 001 (800) 323 - 9653 Telephone: + 44 20 89 44 74 47
MANUFACTURER Phone: 001 (847) 913 - 1113 Telefax: + 44 20 89 44 13 11
[email protected] Fax: 001 (847) 913 - 1488 [email protected]
www.richard-wolf.com [email protected] www.richardwolf.uk.com
www.richardwolfusa.com
BELGIUM / NETHERLANDS FRANCE AUSTRIA
N.V. Endoscopie RICHARD WOLF France S.A.R.L. RICHARD WOLF Austria
RICHARD WOLF Belgium S.A. Rue Daniel Berger Ges.m.b.H.
Industriezone Drongen Z.A.C. La Neuvillette Wilhelminenstraße 93 a
Landegemstraat 6 F-51100 Reims A-1160 Vienna
9031 Gent Drongen Telephone: +33 3 26 87 02 89 Telephone: +43 14 05 51 51
Telephone: +32 92 80 81 00 Telefax: +33 3 26 87 60 33 Telefax: +43 14 05 51 51 45
Telefax: +32 92 82 92 16 [email protected] [email protected]
[email protected] www.richard-wolf.com
www.richard-wolf.be
Marketing Office INDIA
U.A.E RICHARD WOLF India Private Ltd.
RICHARD WOLF Middle East JMD Pacific Square
P.O. Box 500283 No. 211 A, Second Floor
AL Thuraya Tower 1 Behind 32nd Milestone
9th Floor, Gurgaon - 122 001
Room 904, Dubai National Capitol Region
Telephone: + 9 71 43 68 19 20 Telephone: + 91 12 44 31 57 00
Telefax: + 9 71 43 68 61 12 Telefax: + 91 12 44 31 57 05
[email protected] [email protected]
www.richard-wolf.com www.richard-wolf.com

GA-A 176 0
 Contents
1 General information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
1.1 Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
1.2 Intended use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
1.3 Combinations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
1.3.1 Potential equalization . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
1.3.2 Requirements for the products / components of a combination . . . . . . . . . . . . . . . . . . . . 3
1.4 Electromagnetic compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4

2 Illustration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
2.1 Drawing of Treatment Table . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
2.1.1 Legend . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6
2.2 Cable--linked remote control unit for Treatment Table . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

3 Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
3.1 Parking brakes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
3.2 Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
3.3 Installing the table extension . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10

4 Checks and testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

4.1 Daily checks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

5 Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
5.1 General notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
5.2 Positioning the Treatment Table . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
5.2.1 “Emergency OFF” pushbutton . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
5.2.2 Taking out of service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12

6 Reprocessing and maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13

6.1 Reprocessing of device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
6.2 Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
6.2.1 Maintenance intervals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13

7 Technical description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
7.1 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
7.2 Technical data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
7.3 Operating, storage, transport and shipping conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
7.4 Transport of Treatment Table . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
7.5 Spare parts and accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
7.6 Replacing parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
7.6.1 Device fuse of Treatment Table . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
7.6.2 Disposal of the product, packaging material and accessories . . . . . . . . . . . . . . . . . . . . . 16

GA--A 176 I
1 General information

1.1 Symbols

Symbols Meaning

Attention, Caution

Follow the instruction manual

OFF (power/mains)

ON (power/mains)

Equipotentality

Fuse
μ Alternating current (AC)

TYPE B APPLIED PART

Recycle the product separately. Do not discard together with other waste.

Manual control

A Registered Trademark of ETL, a Recognized Testing Laboratory, listing compliance as

Medical Electrical Equipment to standard CAN/CSA C 22.2 No. 601.1 (c) and UL 60601--1 (us)

A Registered Trademark of Underwriters Laboratories, Inc., a Recognized Testing Laboratory,

listing compliance as Medical Electrical Equipment to standard UL 2601--1 and
CAN/CSA C 22.2 No. 601.1.

A Registered Trademark of a Recognized Testing Laboratory, confirm the compliance to the standard
of Medical Electrical Equipment CAN/CSA C22.2 No.60601-1 (c) and ANSI/AAMI ES60601-1 (us)

Identification in conformity with Medical Devices Directive 93/42/EEC only valid if the product and/or
packaging is marked with this symbol. Products of category IIa and above, as well as
sterile products or products with measuring function of category I, are additionally marked with the
code number of the notified body (0124)

1 GA--A 176
1.2 Intended use

The Treatment Table serves to position the patient for diagnostics and
therapy as well as for necessary auxiliary measures required for ESWL
and ESWT (Extracoporal Shockwave Lithotripsy and -- Therapy).

This product is designed exclusively for use by specialized medical per­

sonnel and may only be applied by medically qualified and adequately
trained persons.

1.3 Combinations
The treatment table is designed for use in combination with PIEZOLITH and
PIEZOSON.

. IMPORTANT
In addition to this instruction manual follow the manuals of the products used in
combination with this product.

1.3.1 Potential equalization

The potential equalization cable establishes a direct connection between
a medical electrical device and an equipotential bonding rail.
It serves to equalize differences in potential between enclosures of elec­
trical equipment and firmly installed conductive parts in the patient envi­
ronment.

GA--A 176 2
1.3.2 Requirements for the products / components of a combination

1.5m
1.5m
1.5m The general requirements depend on whether the products /
components are inside or outside the patient environment.

IEC 60601-1, 3. Ed.

Medically used room Non-medically Requirements / measures

used room
inside the outside the Leakage currents to section 16.6
patient environment patient environment IEC 60601-1:2005 / EN 60601-1:2006 *

MP MP
- - Verification of the total patient leakage current
~ ~
MP MP

~ **

MP NMP
**
~ ~
MP NMP
- Verification of leakage currents
a) additional protective earth connection
**
~ - (consult the corresponding manufacturer),

MP
or
NMP b) additional isolating transformer for medical applications **

~
MP NMP

~
MP MP / NMP

**
~

MP NMP Verification of leakage currents

- a) no plugs with metal housing, or
~ ~ b) additional isolation device (to avoid voltage differentials)
Verification of leakage currents
a) common protective earth connection, or
MP MP / NMP b) additional protective earth connection at MP (clarify with the corre­
ponding manufacturer), or
~ ~ c) additional isolation device (to avoid voltage differentials), or
d) no plugs with metal housing in the patient environment

additional "isolating transformer" to IEC/ EN60601-1 additional isolating device to IEC/

Multiple socket strip
** EN 60601-1
Functional connection ~ Power supply grid
MP = medical electrical device to IEC/ EN 60601-1, ANSI/AAMI es60601-1, CSA C22.2 No. 60601-1 08
NMP = non-medical electrical device in accordance with product-specific IEC/EN/UL standards
* When connected via a power bar under standard conditions the earth leakage current of the power bar must not exceed 5 mA.
** e.g. Richard Wolf video cart with "isolating transformer"

3 GA--A 176
 . IMPORTANT!
The persons combining products to form a system are responsible for not impairing the system's compliance with
performance and safety requirements, and that the technical data and the intended use are adequately fulfilled.
Possible electromagnetic or other interference that may occur between the product and other products can cause
faults or malfunctions.
When selecting the system components, make sure that they meet the necessary requirements of the medical envi­
ronment they are used in, in particular IEC/ EN 60601-1 (3. Edition IEC/EN 60601-1, section 16). In case of doubt
contact the manufacturer(s) of the system components.
Do not touch connectors for electrical connections between various components (such as signal input connectors and
signal output connectors for video signals, data exchange, controls etc.) and the patient at the same time.

1.4 Electromagnetic compatibility (EMC)

NOTE: The device or system in the following called product always relates to the Treatment Table 3000.9xx
The product does not have any performance features classified as essential performance features in accordance with IEC/EN 60601-1.
Guidelines and manufacturer's declaration - Electromagnetic emissions
The product is intended for use in the environment specified below. The user should assure that the product is used in such an environment.
Emissions measurement / test Compliance Electromagnetic environment - Guidelines
The product uses HF energy for its internal function.
HF emissions to CISPR 11 Group 1 The HF emission level is extremely low and it is not likely to cause any
interference in nearby electronic equipment.
HF emissions to CISPR 11 Class B
The product is suitable for use in all establishments, including domestic
Harmonic emissions
Class A establishments. This also includes establishments directly connected to
to IEC 61000-3-2 the public low voltage power supply network that supplies buildings used
In conformity with IEC 61000-3-3 “Emission of voltage fluctuations for domestic purposes.
/ flicker"

Guidelines and manufacturer's declaration - Electromagnetic immunity

The product is intended for use in the environment specified below. The user should assure that the product is used in such an environment.
Immunity tests IEC 60601 test level Compliance Electromagnetic environment - Guidelines

 6 KV contact discharge Floors should be wood, concrete or ceramic tile. If

Electrostatic discharge (ESD)
Yes floors are covered with synthetic material, the re­
to IEC 61000-4-2  8 KV air discharge lative humidity should be at least 30%.
 2 KV for power supply lines
Electrical fast transience, bursts Mains/line power quality should be that of a typical
 1 KV for input and output Yes
to IEC 61000-4-4 commercial or hospital environment.
lines
 1 KV line to line
Surge voltage (surges) voltage Mains/line power quality should be that of a typical
Yes
to IEC 61000-4-5  2 KV line to ground commercial or hospital environment.
voltage
Voltage dip for 0.5 cycle
> 95% UT * Mains/line power quality should be that of a typical
Voltage dip for 5 cycles commercial or hospital environment. If the user of
Voltage dips, short interruptions and sup­ 60% UT * the product requires continued operation during
ply voltage variations Yes
Voltage dip for 25 cycles power mains/line interruptions it is recommended
to IEC 61000-4-11
30% UT * that the product be powered from an uninterrupti­
Voltage dip for 5 sec ble power supply or battery.
> 95% UT *
Power frequency (50/60 Hz) magnetic Power frequency magnetic fields should be at le­
field, 3 A/m Yes vels characteristic of a typical location in a com­
to IEC 61000-4-8 mercial or hospital environment.
* NOTE: UT is the line / mains voltage prior to application of the test level.

GA--A 176 4
Guidelines and manufacturer's declaration - Electromagnetic immunity for products that are not life-supporting
The product is intended for use in the environment specified below. The user should assure that the product is used in such an environment.
Immunity tests IEC 60601 test level Compliance Electromagnetic environment - Guidelines
Portable and mobile RF communications equipment should
be used no closer to any part of the product, including ca­
bles, than the recommended separation distance calculated
from equation applicable to the frequency of the transmitter.

Recommended separation distance:

d = 1.2 p P
d = 1.2 p P for 80 MHz to 800 MHz
Conducted HF interference 3 Vrms d = 2.3 p P for 800 MHz to 2.5 GHz
to IEC 61000-4-6 150 kHz to 80 MHz P = Nominal power output rating of the transmitter in watts
Yes (W)
Radiated HF interference 3 V/m (according to the transmitter manufacturer)
to IEC 61000-4-3 80 MHz to 2.5 GHz d = recommended separation distance in meters (m)
Field strengths from fixed RF transmitters, as determined by
an electromagnetic site survey1, should be less than the
compliance level in each frequency range2.
Interference may occur in the vicinity of devices with the
following symbol:

REMARKS:
At 80 MHz and 800 MHz the higher frequency range applies. These guidelines may not apply in all situations. The propagation of elec­
tromagnetic waves is affected by absorption and reflexion from buildings, objects and people.
1 = The field strength of stationary transmitters (e.g. base station for radio phone, earth to earth radio stations,, amateur radio stations, radio
and television transmitters) cannot be exactly predicted in theory. To assess the EMC environment due to fixed transmitters an electromagnetic
site survey should be conducted. If the measured field strength in the location in which the product is used exceeds the applicable compliance
level above, the product should be observed to verify normal operation.
If abnormal performance is observed, additional measures may be required, such as reorienting or relocating the product.
2 = Over the frequency range between 150 kHz and 80 MHz the field strength should be below 3 V/m.

Recommended separation distances between portable and mobile HF telecommunication devices and devices which
are not life-supporting
The product is intended for use in an electromagnetic environment where HF disturbances are controlled.
The user can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile HF telecommunica­
tions equipment and the product.
Separation distance as a function of transmitter frequency (m)
Rated nominal output power of thetrans­
mitter (Watts) 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2.5 GHz
d = 1.2 p P d = 1.2 p P d = 2.3 p P
0.01 0.12 0.12 0.23
0.1 0.38 0.38 0.73
1 1.2 1.2 2.3
10 3.8 3.8 7.3
100 12 12 23
For transmitters rated at a nominal output power not listed in the table above, the recommended separation distance (d) in meters (m) can be
determined using the applicable equation (observe frequency). P = nominal power of the transmitter in Watts (W).
REMARKS:
At 80 MHz and 800 MHz the higher frequency range applies. These guidelines may not apply in all situations. The propagation of elec­
tromagnetic waves is affected by absorption and reflexion from buildings, objects and people.

5 GA--A 176
2 Illustration

2.1 Drawing of Treatment Table

9
4

12

14 13

7 8 1
4 3
6 2 5

11

2.1.1 Legend

1 Mains/power switch 8 Center pad with therapy cutout

2 Power/mains input connector with fuse holder 9 Center pad without therapy cutout (optional)
3 Identification plate 11 “Emergency OFF" pushbutton
4 Connector for cable-linked remote control unit 12 Leg support pad (optional)
5 Equipotential connector 13 Head pad (optional)
6 Parking brake 14 Support pad with mounting clamp (optional)
7 Extension for Treatment Table with paper reel
holder

GA--A 176 6
2.2 Cable--linked remote control unit for Treatment Table

10.5 Horizontal table movements

10.1
10.1 “Transversal forward" button
10.2 “Transversal back" button
10.3 10.4
10.3 “Longitudinal left" button
10.4 “Longitudinal right" button
10.2
10.5 “Horizontal center position" button

10.8 10.6 Vertical table movements

10.6 “Vertical up" button
10.9 10.7 10.7 “Vertical down" button
10.8 “Vertical left side down and right side up" button
10.9 “Vertical left side up and right side down" button

7 GA--A 176
3 Setup
WARNING!
This device is not protected against explosions.
Explosion hazard.
Do not operate this device in areas where there is a danger of
explosion.

WARNING!
Danger if a power supply without protective earth is used.
Danger of electric shock!
Connect the device only to a power supply with protective earth.
. NOTE!
Check that the mains/line voltage is the same as the voltage specified on
the identification plate. Connect the device only with the supplied power
cable or a power cable meeting the same specifications.

CAUTION!
Danger of faults and malfunctions.
To guarantee the safety of the user, the patient and others use only
accessories and spare parts specified by the manufacturer of this
product.
Other accessories or spare parts can cause the emission of
increased electromagnetic radiation or reduced immunity against
interference.

. IMPORTANT!
Medical devices are subject to special precautions with regard to electro-
magnetic compatibility (EMV).
Make sure you observe the notes on EMC for installation and operation.
Medical electrical devices can be influenced by mobile HF communica-
tion devices.
If it is necessary to stack the devices or place them next to each other
and HF interference is observed, make sure you observe the intended
use of the devices.

GA--A 176 8
3.1 Parking brakes

. NOTE!
During treatment the parking brake must be locked.

Z The pedal has 3 positions.

' Position 1: Parking brake engaged (locked)
' Position 2: Parking brake disengaged (free)
' Position 3: Parking brake disengaged (free) and the wheels are
locked in longitudinal direction.

1 2 3

3.2 Preparation
Z Insert plug of remote control unit into socket on treatment table and
tighten locking collar.
Z Connect the power cable.
Z Switch on the power switch.
' The lamp inside the power switch illuminates.
Z The equipotential line of the device can be connected to the equipoten-
tial line/point of the room, using a potential equalization cable.

9 GA--A 176
3.3 Installing the table extension

Z Insert the pins of the table extension into their holders and push down
the table extension as far as it will go (A).
' Lift outer edge of table extension slightly to allow the sections of
square tubing to pass the stop pins (B).
' Check that the pins of the table extension have fully (i.g. up to the
stop) engaged in the holders.

GA--A 176 10
4 Checks and testing
. IMPORTANT!
Run through the checks before and after each use.
Do not use the products if they are damaged or incomplete or have loose
parts.
Return damaged products together with any loose parts for repair.
Do not attempt to do any repairs yourself.

4.1 Daily checks

Z Check device and accessories for damage, hygienic condition and
competeness.
Z Check all connection cables for damage.
Z The labeling must be complete and easy to read.

5 Use

5.1 General notes

CAUTION!
If patients have infectious diseases, the following measures must be
taken:
Before treatment, seal open wounds with impermeable material to
keep any body fluid from being issued.
After treatment disinfect the device, following the disinfectant man-
ufacturer’s instructions.

. IMPORTANT!
For reasons of hygiene use new table tissue for each patient (e.g. tissue
paper, sterile drapes).

. NOTE!
For the treatment of patients, the parking brakes of all system compon-
ents used must be locked.
Attach the table extension where required.

5.2 Positioning the Treatment Table

Position the patient as required, then fine--position the patient using the
positioning buttons of the cable--linked remote control unit for the Treat-
ment Table.

CAUTION!
Danger. Patient or user may get caught when table is moving.
Adjust table only under visual control not to endanger patients or
others. Ensure that there are no objects stopping the table move-
ment.

11 GA--A 176
5.2.1 “Emergency OFF” pushbutton

. IMPORTANT!
The table movement can be stopped at any time by pressing the “Emer-
gency OFF” pushbutton (11).

To reset the “Emergency OFF” pushbutton (11), turn the pushbutton

clockwise as far as it will go and release it.

11

5.2.2 Taking out of service

Z To take the device out of service, switch off the power switch and
disconnect the device from the power supply / mains.

GA--A 176 12
6 Reprocessing and maintenance

6.1 Reprocessing of device

WARNING!
Prevent humidity from entering the device.
Danger of electric shock!
Before reprocessing switch off and disconnect the device from the power
supply / mains.

. NOTE!
For a description of the surface cleaning and disinfecting agents for devi­
ces and universal device carts / trolleys and utility carts approved by Ri­
chard Wolf, please refer to manual GA-J020 "Reprocessing of RICHARD
WOLF Heat-stable Instruments".

. IMPORTANT!
Disinfect the padding of the treatment table top using surface disinfectant
certified for use with patients on a daily basis.
Follow the disinfectant manufacturer’s instructions.

. IMPORTANT!
Make sure that no humidity enters the device. Do not use any cleaning or
scouring agents or solvents for the care of the device!

6.2 Maintenance
. IMPORTANT!
In your inquiries or correspondence please always indicate the model and
serial number on the identification plate. Further documentation is avail-
able from the manufacturer upon request.

6.2.1 Maintenance intervals

. IMPORTANT!
To prevent incidents caused by ageing and wear, the device and its ac-
cessories must be serviced at adequate intervals. Depending on the fre-
quency of use, however at least once a year, an expert must check the
device and carry out a safety test.

13 GA--A 176
7 Technical description

7.1 Troubleshooting
. IMPORTANT!
If you cannot eliminate a problem with the help of this table, please con-
tact our service department or return the device for repair.
' Do not attempt to do any repairs yourself!

Problem Potential cause Intervention

Power switch is not ON 'Switch power switch ON
Device has no function: Power cable is not connected 'Connect power cord
-- Power switch is not illuminated No power supply / no supply voltage 'Check in--house power supply
Defective fuse 'Change line fuse
Device without function: Remote control unit is not connected 'Connect remote control unit
-- Power switch is illuminated Remote control unit defective 'Change remote control unit

7.2 Technical data

Voltage Frequency Power Current Fuse
Treatment
consumption rating
Table
Vμ Hz VA A A
3000.901 200 -- 240 50 / 60 240 1,0 T 2.5 L
3000.902 100 -- 120 50 / 60 240 2,0 T 4.0 L

Electrical safety to EN / IEC 60601--1

Electromagnetic compatibility (EMC) to EN / IEC 60601--1--2
Medical Devices Directive 93/42/EEC Class I
Protection against electrical shock Type B applied part
Protection class in acc.with IEC / EN 60601--1;
I
(UL 60601--1 / CSA C22.2 No.601.1 -- for USA)
Degree of protection against the ingression of liquid IP 20 (Not protected)
Mode of operation/duty factor Continuous operation
This device is not protected against explosions
Degree of protection in the presence of flammable
(Do not operate this device in areas where explosive
gasses:
substances are present)

Travel: Transversal 100 mm

Longitudinal 100 mm
Vertical 250 mm
Traverse rate: Transversal 3 mm/sec.
Longitudinal 3 mm/sec.
Vertical 6 mm/sec.
Table tilt (Trendelenburg) up to ¦ 10
Carrying capacity maximum 135 kg (296 lbs)
Carrying capacity of extension maximum 80 kg (175 lbs)
Weight approx. 120 kg (approx. 264 lbs)
Dimensions of table L x W x H 1880 mm x 780 mm x 750 to 1000 mm
Dimensions of extension L x W 400 mm x 780 mm

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7.3 Operating, storage, transport and shipping conditions
+ 10C to + 40C , 30% to 75% rel. humidity,
Operating conditions
atmospheric pressure 700 hPa to 1060 hPa
+5 C to + 40C , 10% to 90% rel. humidity,
Storage, transport and shipping conditions
atmospheric pressure 700 hPa to 1060 hPa

. NOTE!
To prevent damage during the transport or shipment of the products we recommend using the original
packaging material.

7.4 Transport of Treatment Table

Z Lower the table top as far as it will go and adjust it horizontally to cen-
ter position.
Z When passing over obstacles, such as uneven surfaces, small steps
etc., which are higher than 1.0 cm, use suitable bearing plates or
wedges.
Z Acceleration / deceleration ± 3 G
Z After transport always engage the parking brakes to lock the table in
place.

7.5 Spare parts and accessories

Units Model/type Designation

1 72 315.008 Fuse for Treatment Table T 2.5 AL
1 72 315.015 Fuse for Treatment Table T 4.0 AL
1 72 325.302 Power cord (Europe), 5.0 m
1 72 325.319 Power cord (North America), 3.66 m
1 64 235.182 Cable--linked remote control unit
1 72 325.093 Equipotential cable
1 64 211.067 Extension for treatment table, gray
1 64 211.142 Extension for treatment table, turquoise
1 64 005.927 Center foam padding with therapy cutout, gray
1 64 005.1045 Center foam padding with therapy cutout, turquoise
1 3000.971 Center foam padding without therapy cutout, gray
1 64 004.257 Center foam padding without therapy cutout, turquoise
1 3000.941 Lateral bracket, black
1 64 005.966 Head support padding, gray
1 74 020.021 Head support padding, turquoise
1 64 005.965 Leg support padding, gray
1 74 020.022 Leg support padding, turquoise
1 74 020.023 Positioning wedge, turquoise
1 64 004.249 Support padding with fastening clamp, gray
1 64 005.964 Support padding, gray
1 74 010.072 Handle
1 74 008.088 Paper roll holder
1 74 020.025 Paper roll
' further accessories on request

15 GA--A 176
7.6 Replacing parts

7.6.1 Device fuse of Treatment Table

CAUTION!
The specification of the device fuses must correspond with the fuse
ratings on the identification plate.
Use only the fuses specified in the spare parts list.

L Power input connector with fuse holder

2 2

3
4

1 3

Z Switch off the device and disconnect the power cord from the power
input connector of the device.
Z Push together the catches [2] of the fuse holder [1] and pull out the
fuse holder.
Z Remove the blown fuses and install new ones [3].
Z Reinstall the fuse holder [4]. Push it in until it audibly clicks.

7.6.2 Disposal of the product, packaging material and accessories

For the disposal observe the relevant regulations and laws valid in your
country.
' For further information please contact the manufacturer.

GA--A 176 16