CE mark/Conformity: This is a Class I medical device according to the Council Directive 93/
42/EEC concerning medical devices and is compliant with the Directive version currently in force
at the time of product sale. The manufacturer declares the conformity of this product with the
essential requirements of the Council Directive 93/42/EEC concerning medical devices
according to Appendix I, as well as the implementation of an assessment procedure required for
Class I product conformity under Appendix VII and documents this with the CE mark.
ETL mark: Intertek tested the product for the USA and Canada. ETL classification regarding risk
of electric shock and fire, as well as mechanical hazard in accordance with ULSTD 60601-1;
CAN/CSA STD C22.2 NO.601.1.
We at TRUMPF Medical are constantly improving our products.
Therefore, we reserve the right to make changes to the format, equipment, and technology at any time.
Reprinting, copying or translating this document, in whole or in part, is forbidden without the express written
permission of TRUMPF Medizin Systeme GmbH + Co. KG.
TRUMPF Medizin Systeme GmbH + Co. KG expressly reserves all rights under copyright law.
Within the bounds of the legal requirements, the manufacturer is responsible for the technical safety characteristics
of this apparatus only if the maintenance, repairs, and modifications to this apparatus are performed by him or
by someone appointed by him and in accordance with his instructions.
This manual and any repair steps specified herein must be observed
and followed. Repairs may be performed only by service
technicians from TRUMPF Medizin Systeme GmbH + Co. KG or by
personnel authorized, trained, and certified by Trumpf Medical.
Only the repairs and settings listed in this guide or known to you
from the appropriate service training by our technical support
service may be performed! Repairs not covered in these instructions
may be performed only after consulting with the TRUMPF Medical
Technical Service department or by Trumpf Medical itself.
Unauthorized or provisional repairs are not permitted even if a
customer so requests. All laws, legal regulations and standards must
be observed and adhered to. Only use original spare parts
designated by Trumpf Medical as spare parts. Defective parts that
are not in proper working order must be replaced with original
spare parts, even if it is beyond the scope of the repair order! After
repairs, return cables to their original installed positions and avoid
any shearing or crushing. After each repair, recheck the electrical
connections against the circuit diagram before performing a
functional test. After all repairs or adjustments, a functional test has
to be performed in accordance with these instructions or relevant
standards. Recheck the position of the cables during and following
all equipment positions!
Important Information
Germany
Only deliver the device to the customer in the tested state with
full functionality! Hand-over to the customer must be effected in
writing with confirmation from the customer. The functionality
must be demonstrated to the customer!
Proper use of and instructions on how to operate the TruSystem
7000 operating table can be found in the instruction manual.
The Service Center will be grateful for any corrections and tips for
more efficient repairs. For questions or feedback please contact:
TRUMPF Medizin Systeme GmbH + Co. KG
Technical Customer Service
Carl-Zeiss-Str. 7–9
07318 Saalfeld
Germany
• Important: use only stainless-steel screws of strength class 70 on
the operating table! Comply with the torque specified for
tightening screws.
•For all screws ≥ M4 without split lock washers, use a mediumstrength screw locking agent. Notice, the agent can be
loosened again by heating the screws with a hair dryer.
• Protective work clothing:
Do not wear clothing which can become caught in the
equipment. Shirt and jacket sleeves should be buttoned or rolled
up.
Tie or put up long hair.
Tuck the ends of scarves, ties or shawls into your clothing or pin
them down. Loose clothing can be a hazard!
For activities that are moderately dangerous for the eyes, wear
protective glasses (e.g., for soldering work or when removing
taut springs and fasteners, when hammering in or hammering out
pins or similar parts).
Safety information
Protection against
infection
• Do not perform any activity that may put other people in danger
or that can make the device a source of danger!
• Store removed housing and other machine parts in a safe place
while working. Always store tools or removed parts in such a
way that no one can stumble and fall over them. Keep the area
around the device clean and tidy during and after maintenance
work.
• Do not let any screws, nuts or other parts fall into the column.
Immediately remove any parts that fell in. Parts that have not
been removed can damage other components or cables when
the OR table is adjusted. Important! The operating table may not
be released to the customer if parts fell in and were not removed.
• After performing work, reattach protective devices and replace
them if necessary. This includes, for example, covers, cable ties,
cable mounts, cable shields, ground and potential conductor
connections, and power connections. Check connection of
equipotential bonding conductor/grounding cable in
accordance with the applicable standards.
• Risk of infection throughout the entire hospital! Follow all safety
measures, behavioral rules and hygiene requirements. Follow
the requirements of the medical facility for protecting against
infection.
• Perform maintenance and repair work only on disinfected
operating tables! Disinfection is performed by the medical
facility.
• Perform work in the OR area only with appropriate
authorization.
• Immediately seek a physician in the event of a complaint of
possible infection. Inform the doctor you were working in a
hazardous area - even if this was several months prior.
Prevention against
infection
2.2Liability
2.3Disposal
• Ask the doctor about possible risks and discuss how to avoid
them in your work as a medical service technician.
• Get a hepatitis B inoculation if advised by a physician. A booster
shot is required every 3 to 5 years. The incubation period for
hepatitis B is 1 to 6 months!
TRUMPF Medizin Systeme GmbH + Co. KG IS LIABLE ONLY for
reliable and proper functionality of the operating table IF
• installation, modification, and repairs are performed by
Trumpf Medical service technicians or by personnel authorized,
trained, and certified by Trumpf Medical.
• the operating table is used properly in accordance with the
instruction manual.
The products must be recycled in an environmentally friendly
manner. Disposal, including that of individual parts, must be
environmentally friendly, i.e., in accordance with the legal
regulations currently in force. For information on proper disposal of
old equipment, please contact either Technical Service at
Trumpf Medical, your local sales representative, or the appropriate
national agency Trumpf Medical will take back your old equipment
or products that are defective or no longer used. For detailed
information, contact Technical Service.
When decommissioning an operating table, the lithium ion batteries
have to be removed by a Trumpf Medical service technician or a
person trained and authorized by Trumpf Medical. Return removed
and unusable batteries in suitable packaging to Trumpf Medical
Technical Service. Important: the returns must be declared as
hazardous materials of class 9/UN3480! Trumpf Medical will
take responsibility for the environmentally proper disposal of the
battery.
Important information in these repair instructions is marked with
symbols and keywords. Keywords such as DANGER, WARNING
or CAUTION indicate the level of danger involved. The symbols
emphasize the message visually. Additional symbols can indicate
injury hazards or danger to life and limb. The measures to prevent
hazards must be observed.
Refers to a directly imminent danger that will result in death or
serious injuries if the appropriate precautionary measures are not
taken.
Refers to a directly imminent danger that can result in death or
serious injuries if the appropriate precautionary measures are not
taken.
Explanation of Symbols
DANGER
Risk of death (for example, electric shock)!
WARNING
Risk of death!
CAUTION
Risk of injury (for example, crushing)!
Refers to a possible danger that can lead to slight to moderate
injury or damage to the equipment if the appropriate precautionary
measures are not taken.
CAUTION
Risk of material damage!
Refers to a possible danger that can lead to equipment damage if
the appropriate precautionary measures are not taken.
NOTE
Additional useful information and tips.
TEST
Performing functional tests, measurements and tests
[1] Column keypad
[2] Remote control
[3] Seat section
[4] Back section
[5] Motorized leg section joint with fixture L
[6] Side rail for seat section
[7] Motorized back section joint
[8] Side rail for back section
[9] Fixture S
[10] Insertion opening for extension adapter
[11] Bayonet locking mechanism for extension adapter
[12] Control unit connector socket (head and foot end)
[13] Table base
[14] Connector pin for equipotential bonding cable
[15] Connector socket for power cable
[16] wheel
[17] Wheel for table base support (directional travel/drive mode)
[18] Key for emergency release of the table 's base (under the
label)
[19] Power cable
[20] Equipotential bonding cable
[21] Side rail for leg section joint
*1
[22] Head end
[23] Foot end
[24] Left side
[25] Right side
The ▸System◂ menu and its functions are available only with the
Cable remote control TS7000 U (#1767067).
The ▸System◂ (secured) submenu is located under the ▸Settings◂
menu item on the touch screen. This menu item is passwordprotected and accessible only to trained Trumpf Medical service
technicians. The password, which is set at the factory, is available
from the Service Center.
The individual numbers (0 to 9) of the password (code) are set
using the arrow keys [i16]/[i17]/[i47] and [i48]. The cursor
flashes at the currently active position. After it is entered, confirm the
password with the OK [i31] key.
The ▸System◂ menu contains the following displays and settings:
–1. ▸Display of HW/SW states◂
–2. ▸Block RC on Key Error◂
–3. ▸Show Key Error Status◂
–4. ▸Component Test◂
–5. ▸Motion Sensor Test◂
–6. ▸Key test FB◂
–7. ▸LED test FB◂
–8. ▸Start Flash update◂
–9. ▸Error memory exp.◂ (export)
– 10. ▸End emergency mode◂
– 11. ▸Reset or table◂
– 12. ▸Factory defaults◂
– 13. ▸Network address◂
– 14. ▸Set IR code◂
– 15. ▸Change password◂
– 16. ▸Acceleration sensor active◂
– 17. ▸Display battery state◂
– 18. ▸ISM parameters◂
– 19. ▸SD Card Info◂
– 20. ▸Show all messages◂
– 21. ▸Touch sensors inactive◂
– 22. ▸Test touch sensors◂
– 23. ▸Request service mode◂
NOTE
Standby mode is switched off for most of the settings in the
▸Settings◂ menu.
9.▸Error memory exp.◂ (export)
No function at this time.
10. ▸End emergency mode◂
No function at this time.
11. ▸Reset or table◂
No function at this time.
12. ▸Factory defaults◂
No function at this time.
13. ▸Network address◂
The LAN and W-LAN IP address is shown.
Important: the IP address must be read from right to left. For
example, 1.2.3.4 is shown on the display. The correct IP
address is 4.3.2.1.
14. ▸Set IR code◂
No function at this time.
15. ▸Change password◂
You can change the password that has been set at the factory.
The individual numbers (0 to 9) of the password are set using
the arrow keys [i16]/[i17]/[i47] and [i48]. The cursor flashes
at the currently active position. After it is entered, confirm the
password with the O
K [i31] key.
16. ▸Acceleration sensor active◂
The motion sensor can be switched off if frequent shaking in the
area prevents standby mode. The sensor for activating the
remote control from the standby mode is active when the
display is marked by an * (asterisk). To activate or deactivate
the sensor press the OK [i31] key.
17. ▸Display battery state◂
Function is not active.
18. ▸ISM parameters◂
Function is not active.
19. ▸SD Card Info◂
Menu item delivers information on the version of the text and
graphics files.
20. ▸Show all messages◂
The operating table transmits system information in an
encrypted code to the remote control. The most important
system information (e.g., error messages, status reports) are
stored in plain text messages and are displayed on the remote
control. Upon activating the ▸Show all messages◂ function, all
system information is displayed. The ▸Show all messages◂ is
As the medical products from Trumpf Medical are distributed
worldwide, uniform guidelines for electrical retesting should be
used.
According to the IEC 60601-1 standard, the limit values according
to the CF classification apply when testing applied parts. Based on
the design type, the Trumpf Medical electric operating tables only
include one applied part of Class B.
Furthermore, the Trumpf Medical product-specific prescribed retests
and safety checks are obligatory.
GermanyInternational
In Germany, initial testing and
retesting of electrical devices
are governed by the stipulations
of the accident prevention
regulation BGV A3.
VDE 0751-1 is the standard that
In countries with different
national legislation, the countryspecific standards and
guidelines for the retesting of
electrical medical devices are
mandatory.
serves as the basis for retesting
of electrical medical devices.
Therefore in accordance with
the VDE 0751-1 standard noted
above, the specifications based
on IEC 60601-1 are definitive
for Trumpf Medical medical
devices.
All maintenance work must be carried out with the help of the
maintenance protocol and take into consideration the spare or
wearing parts list and the lubrication plan (see page 284).
Conduct a complete functional test after service work is completed.
The TruSystem 7000 operating table contains two lithium ion
batteries. Because of their size (number of individual cells plugged
in, amount of lithium contained), they are classified as a hazardous
material. There is a risk of explosion in case of fire. As a result, there
are legal ordinances regarding the handling, deployment, and
installation of this type of battery.
The lithium ion batteries were specially developed by
Trumpf Medical. An electronic protective circuit on a circuit board
in the housing monitors the threshold values of the current / voltage
data. The electrical connection outward is provided through a
7W2 D-Sub socket.
Technical parametersThreshold values
Nominal voltage (3.7 V/cell)40.7 V
Nominal capacity (2.4 Ah/cell)4.8 Ah
Handling on/in
operating table
Working voltage range37 V…45.1 V
Shutdown undervoltage (2.4 V / cell)approx. 26 V
Shutdown overvoltage (4.35 V / cell)approx. 48 V
Shutdown overcurrent20 A
Self-discharge current with active battery180 μA
Max. discharge current over 2 min.8 A
Max. continuous discharge current4.8 A
Charging time with 3 A charge currentApprox. 3 hrs
Storage temperature range– 40 °C to 80 °C
Max. internal battery temperature during
discharge
Max. internal battery temperature during
charge
Battery Position
1on power supply
60 °C
40 °C
2on lift motor
The battery is connected using cable W134 (#1538234) for
battery 1 and W172 (#1538235) for battery 2. The battery is
directly connected or disconnected using the corresponding
connection cable in the operating table. There are no special
measures, such as a connection sequence on the power supply. A
battery is inserted or removed using the carrying strap. The column
base has two diagonal guide pins that position the battery housing.
Battery 1 is secured in place by a special plate (battery
bracket_power supply). Battery 2 is secured by the spiral cable
holder_rear.
StorageFor extended battery storage, the manufacturer recommends a
charge level of approx. 40 %. For storage, as a guide
Trumpf Medical recommends a no-load voltage of approx. 43 V
for the battery charge level. Batteries should be stored in a cool, dry
place.
Charging/
discharging
The batteries are usually charged in the operating table by the
power supply. During external charging, the maximum charge
current equals 2.4 A. The maximum charge voltage of 45.1 V may
not be exceeded. A rechargeable battery is full (stops charging)
when the charging current falls below 100 mA for at least 1 minute.
The maximum discharge current for a period of no more than 2
minutes may not exceed 8 A. Important: there is no temperature
monitoring when the battery is used as an external energy source.
The threshold temperatures may not be exceeded.
To prevent hazards, the battery state is monitored automatically in
the operating table.
TransportAll batteries must undergo a Trumpf Medical certified safety test
before being released for general use. To ship a battery, use the
manufacturer's special transport packaging (reusable packaging).
DisposalReturn removed and unusable batteries in suitable packaging to
Trumpf Medical Technical Service. Important: the returns must be
declared as hazardous materials of class 9/UN3480!
Trumpf Medical will take responsibility for the environmentally
proper disposal of the battery.
Before beginning repair work, prepare the operating table in
accordance with the following work steps:
Preparing the Operating Table
1.
CAUTION
Danger of infection!
Note to hygienic conditions at the site, and clarify any
questions concerning protection against infection with the
doctor in charge. Before beginning work, have the medical
facility confirm that all necessary measures for protection
against infection have been implemented. Perform repairs
only after protection of personnel against infection is ensured.
2.Lock operating table (brake)
3.Move to the level position on the operating table.
4.Remove all table components and accessories from the
operating table and store them in a safe place.
5.Move the operating table to the most elevated position.
6.Disconnect the operating table from the external power supply
(first remove the power cable plug from the insulated contact
receptacle and then from the connection socket on the table
base).
7.Remove the pad from the table top so that it is not damaged
during repair.
During repair work, do not make any adjustments to the operating
table except those explicitly specified.
Open1.Prepare the operating table (see chapter 7 on page 29).
2.Turn off the operating table.
CAUTION
Risk of injury due to capacitor voltage.
Switch off repeatedly if needed. No LEDs may be illuminated
on the column keypad!
3.Disconnect the lowest column cover [1] from the pot [2] (2
screws [3]).
4.Carefully slide the column cover upward, tighten the retaining
screw [4] on the Trendelenburg assembly [5], and place the
column cover [6] on the retaining screw.
Close1.Grasp the column cover, remove the holding screw from the
Trendelenburg assembly and guide the cover carefully
downward.
2.Install the lowest column cover on the pot (2 screws).
3.Put on the pad.
4.Switch on the operating table at the column keypad.
5.Connect the operating table to the external power supply.