Dewert 2054XLE User manual

Dewert User Manual 2000XL Series–Updated 03.2023/4 MDR Page 1 of 17
User Manual
2000XL series model
Dear customer,
Congratulations on purchasing a product of outstanding quality.
Use of the best materials from renowned suppliers guarantees years of trouble-free operation, provided the
device is handled correctly and as intended in accordance with the conditions described in the user manual.
In the unlikely event you need to make a claim, please contact us.
We welcome suggestions from the users of our products.
Contents
1. Safety information.................................................................................................................................... 2
1.1 Applied symbols .............................................................................................................................. 2
1.2 Applied standards............................................................................................................................ 2
1.3 Safety regulations............................................................................................................................ 2
1.4 Intended purpose............................................................................................................................. 3
1.5 Information on setup and use.......................................................................................................... 3
1.6 Commissioning................................................................................................................................ 3
1.7 Safety notices ................................................................................................................................. 4
1.8 Entrance area.................................................................................................................................. 4
1.9 Model designation and type labelling .............................................................................................. 5
1.10 Meaning of the serial number.......................................................................................................... 5
2. Operating manual.................................................................................................................................... 5
2.1 Table design.................................................................................................................................... 5
2.2 Height adjustment............................................................................................................................ 6
2.3 Head part adjustment...................................................................................................................... 6
2.4 Adjustment of other sections........................................................................................................... 7
2.5 Movability (model dependent or optional) ....................................................................................... 7
2.6 Additional equipment....................................................................................................................... 8
2.7 Echocardiography tables................................................................................................................. 9
3. Additional accessories (for user-specific table configuration)................................................................. 9
4. Technical data........................................................................................................................................ 10
4.1 Individual models of the 2000XL series.........................................................................................10
4.2 Technical data for electric motor ................................................................................................... 13
4.3 Technical data for hydraulic system..............................................................................................13
5. Cleaning instructions.............................................................................................................................13
6. Maintenance and technical inspection ..................................................................................................14
7. Safety devices.......................................................................................................................................15
8. Reporting obligation............................................................................................................................... 16
9. Disposal .................................................................................................................................................16
10. Declaration of Conformity ...................................................................................................................... 17
Subject to changes in materials and construction as a result of technical progress.
K.H. DEWERT GmbH
Vollmestr. 7
33649 Bielefeld
Germany
Tel. +49 / 521 400 27-0
Fax +49 / 521 400 27-27
[e-mail]
www.khdewert.de

Dewert User Manual 2000XL Series–Updated 03.2023/4 MDR Page 2 of 17
1. Safety information
1.1 Applied symbols
Safety instructions and key sections in these operating instructions are marked with the exclamation mark
symbol on the left. Please pay particular attention to these instructions and sections.
Symbols used on the device, depending on the respective equipment:
Observe instructions for use:
Risk of injury due to being pinched or crushed:
Caution, potential hazard:
Connection for potential equalisation according to DIN 42801:
1.2 Applied standards
This device has been designed and manufactured in accordance with national and international regulations.
This ensures a very high level of equipment safety.
The models described here comply with the following regulations and directives:
Regulation (EU) 2017/745
DIN EN IEC 60601-1
DIN EN ISO 14971
Pre standard DIN VDE V 0750-2-52-2 (VDE V 0750-2-52-2):2021-10 partly based on
DIN EN IEC 62353
DIN EN ISO 10993-5/-10
DGUV Regulation 3
This device is a Class 1 medical device according to Regulation (EU) 2017/745 (MDR).
1.3 Safety regulations
This section contains a summary of the most important safety information:
Correct operation of the device is essential for safe operation. Therefore, please familiarise yourself with the
contents of these instructions for use before using the device. We recommend that you keep these
instructions for use near the device for future reference.
The device may only be used by authorised, instructed and competent persons who are sufficiently familiar
with its adjustment mechanism or have read and understood the operating manual fully. The manufacturer
cannot be held responsible for damage caused by or involving unauthorised persons. No third-party devices
may be installed without consultation with us or brought in the direction of movement of the table in such a
way that a possible hazard potential arises.
The user must ensure that the device is not accessible to unauthorised persons or cannot be operated by
unauthorised persons even when left unattended. When leaving the device, it should be secured in such a
way that unauthorised adjustment is impossible.
Important: Never leave the device unattended or accessible to third parties when it is ready for operation.
This product is not approved for the American market. Distribution and use of the product in these
markets, including through third parties, is prohibited by the manufacturer.

Dewert User Manual 2000XL Series–Updated 03.2023/4 MDR Page 3 of 17
Keep a sufficient safety distance to the device during all adjustment procedures. Special attention
must be paid to the arms, hands, legs and feet of the user and the patient - RISK OF CRUSHING!
Make sure that there are no objects located directly around or above / underneath the device!
1.4 Intended purpose
The table is used for the ideal positioning of patients for the purpose of curative and disease treatment,
examination, massage and health therapy.
Table operation and patient positioning on the table may only be performed by professionally trained persons
who have been instructed in its use or who, through experience with other similar medical devices, have
knowledge of its proper use, taking into account possible hazards.
Equipped with the options of movability (not wheel-lifting/fixing mechanism), side guards and push handle, the
intended purpose of the table is extended and also provides for the ideal positioning of patients for the
purpose of transport to pre-treatment or post-treatment locations. Patient positioning during the recovery
phase after a medical procedure is also permitted under supervision.
Otherwise, the device must only be moved within the room for cleaning or patient access.
This device has been developed exclusively for use indoors and in normal ambient conditions and can be
used in the following areas: laboratories, medical practices, examination and treatment rooms, hospitals,
clinics, physiotherapy practices, occupational therapy centres and doctors’ surgeries.
This table is not classed as surgical furniture and must, therefore, not be used for surgical purposes.
The expected service life is 10 years or 100,000 drive cycles (double stroke = 1x up and down).
1.5 Information on setup and use
When packed, the device may be exposed to the following environmental conditions for approx. 3 months:
Transport/Storage temperature: -20° to +50°C
Operating temperature: +10° to +40°C
Relative humidity: 30% to 75%
Air pressure: 800hPa to 1060hPa
When transporting the device in a vehicle, it must be secured properly against moving. To do so, lock the
castors (optional equipment) and ensure further safety measures.
When setting up the device, do not lift it at the head part, as this may damage the head part and/or the
release mechanism.
Hold and lift the table on the left and right-hand side of the underframe. The table must stand securely on its
feet or castors on a level, flat and solid surface. Before use, activate the brakes on the castors and make sure
they are working properly.
When transporting the table, take hold of the underframe, NOT the upper frame.
1.6 Commissioning
The device is ready for use upon delivery. Remove the power cable from the film packaging on the
underframe of the table and connect it properly to a permanently installed mains socket. When routing the
power cable, make sure the cable cannot be crushed, rolled over or otherwise damaged.
Lock the castors (optional) or the wheel system (optional). As the operator, carry out a thorough and precise
function check once the device has been set up. Prior to commissioning, clean the device and remove any
contamination from transport. Make sure that no connecting cables from the hand or foot switch to the motor
are trapped in the mechanism and thus damaged.
Operation in potentially explosive atmospheres is not permitted.
Installation instructions: In order to exclude possible jamming / crushing between the device or one of its
parts and an object, no objects must be located in the movement area of the device.

Dewert User Manual 2000XL Series–Updated 03.2023/4 MDR Page 4 of 17
1.7 Safety notices
This table may only be used for its intended purpose. Any other use is strictly prohibited and possibly
dangerous. The manufacturer cannot be held responsible for damage caused by improper use. Patients may
only be positioned in preparation for treatment/examination by professionally trained persons.
Please note: This table is not classed as surgical furniture.
Prior to and when adjusting the height of the table, make sure that no persons or objects are located in the
adjustment range of the table and that nobody has their hands on the underframe.
The following basically applies: Never reach into or under the frame of the table when adjusting the height.
Height adjustment can result in injury if the user does not pay due care and attention. Therefore, take great
care when performing this procedure.
When adjusting the upholstery parts, make sure that no persons or objects are in the adjustment range. Make
sure that no persons reach under the upholstery part or lean on the underframe.
Important for the user: When adjusting the upholstery parts, do not reach under the spacers located beneath
the upholstery parts.
Always use both hands when adjusting the lying surface elements: Use one hand to operate the adjustment
mechanism and the other hand for the lying surface adjustment.
The lying surfaces and the underframe are not anti-static as standard.
Our products are not intended for use in wet rooms and must under no circumstances be cleaned using so-
called bed washers. This would irreparably destroy the product.
The head part and armrests are only intended to support the patient and must not be used for sitting.
Do not stand on the table or its parts.
If the underframe is designed with movability (optional), all the castors must always be locked before using
the table.
Do not put a damaged device into operation.
Disconnect the device from the mains (power supply) in the event of a fault or during maintenance work. To
disconnect, be sure to grasp the plug, not the power cable.
This device must not be modified without the express permission of the manufacturer.
When transporting the table, take hold of the underframe, NOT the upper frame.
Persons who are not familiar with the use of the table or who do not have knowledge of its proper use through
experience with other similar medical devices must not be left unattended with the table.
When the table is ready for use, it is forbidden to stay under the table or its parts.
Do not stand on the foot switch rail (optional).
1.8 Entrance area
The following pictures show, depending on the number and adjustment of the upholstery parts, the table’s
entrance area. This is characterized by a dark grey surface. The entrance area represents the area in which a
patient / person can sit down or stand up when used as intended.

Dewert User Manual 2000XL Series–Updated 03.2023/4 MDR Page 5 of 17
Mod.
2000, 2001, 2006, 2007, 2052, 2053, 2600,
2605, 2610, 2615
Mod.
2030, 2035, 2054, 2150, 2155, 2550,
2551
Mod. 2100, 2105, 2110;
Mod. 2114, 2115
(nur Fläche mit *)
Mod.
2008, 2009
Mod.
2010, 2011
Mod.
2650, 2651, 2655, 2656, 2552
1.9 Model designation and type labelling
The exact model designation depends on the choice of frame colour:
-00 white powder coated (RAL 9010);
-03 white aluminium powder coated (RAL 9006);
-04 grey aluminium powder coated (RAL 9007)
and the type of selected height adjustment:
E = electromotive;
/H = hydraulic
The type plate is attached to the underframe on one long side of the table. It provides information about key
table data. The following symbols are listed there (by way of example), their meanings are:
Read the operating
manual
Serial no.
Applied part Type B
Caution, potential
hazard
Max. load
capacity
CE mark
Date of manufacture
Product may only
be used in dry
rooms
Do not dispose of with
household waste
Address of
manufacturer
Protective
insulation,
protection class II
1.10 Meaning of the serial number
The serial no. is located on the type plate or shown separately next to the type plate of the table. This number
is unique and firmly linked to this specific individual product. It enables us to identify this table model and
trace back assemblies/safety-relevant components at any time. Please always state this serial number when
enquiring about spare parts.
2. Operating manual
2.1 Table design
When designing the table frames, special emphasis was placed on functional and operational safety. The
number of possible pinching points has thus been minimised, while remaining ones have been covered or
head part lying surface
head part lying surface
lying surface
*
head part lying surface foot part
head part lying surface foot part
head part lying surface foot part