Dürr Medical CR 35 VETwin User manual

EN
CR 35 VETwin
Installation and operating instructions
9000-608-160/02
*9000-608-160/02*
2107V004

Contents
Important information
1About this document .. . . . . . . . . . . . . 3
1.1 Warnings and symbols .. . . . . . . 3
1.2 Label .. . . . . . . . . . . . . . . . . . . . 4
1.3 Copyright information .. . . . . . . . 4
2 Safety .. . . . . . . . . . . . . . . . . . . . . . . . . 5
2.1 Intended use .. . . . . . . . . . . . . . . 5
2.2 Improper use .. . . . . . . . . . . . . . . 5
2.3 General safety information .. . . . . 5
2.4 Specialist personnel .. . . . . . . . . 5
2.5 Electrical safety .. . . . . . . . . . . . . 5
2.6 Only use original parts .. . . . . . . . 5
2.7 Transport .. . . . . . . . . . . . . . . . . . 6
2.8 Disposal .. . . . . . . . . . . . . . . . . . 6
2.9 Protection from threats from the
Internet .. . . . . . . . . . . . . . . . . . . 6
Product description
3Overview .. . . . . . . . . . . . . . . . . . . . . . . 7
3.1 Scope of delivery .. . . . . . . . . . . . 8
3.2 Accessories .. . . . . . . . . . . . . . . . 8
3.3 Optional items .. . . . . . . . . . . . . . 8
3.4 Consumables .. . . . . . . . . . . . . . 8
3.5 Wear parts and replacement
parts .. . . . . . . . . . . . . . . . . . . . . 8
4Technical data .. . . . . . . . . . . . . . . . . . . 10
4.1 Image plate scanner .. . . . . . . . . 10
4.2 Image plate .. . . . . . . . . . . . . . . . 12
4.3 Type plate .. . . . . . . . . . . . . . . . . 13
4.4 Evaluation of conformity .. . . . . . 13
4.5 Declaration of conformity .. . . . . . 14
5 Operation .. . . . . . . . . . . . . . . . . . . . . . 15
5.1 Image plate scanner .. . . . . . . . . 15
5.2 Image plate .. . . . . . . . . . . . . . . . 17
5.3 Light protection cover .. . . . . . . . 17
5.4 Flexible foil cassette .. . . . . . . . . 17
5.5 Rigid foil cassette .. . . . . . . . . . . 18
5.6 Foil sleeve .. . . . . . . . . . . . . . . . . 18
5.7 Rigid cassette .. . . . . . . . . . . . . . 18
5.8 Stylus .. . . . . . . . . . . . . . . . . . . . 18
5.9 Bite protector (optional) .. . . . . . . 18
5.10 Light protection screen .. . . . . . . 18
Assembly
6 Requirements .. . . . . . . . . . . . . . . . . . . 19
6.1 Installation/setup room .. . . . . . . 19
6.2 System requirements .. . . . . . . . . 19
6.3 Monitor .. . . . . . . . . . . . . . . . . . . 19
7 Installation .. . . . . . . . . . . . . . . . . . . . . . 19
7.1 Carrying the unit .. . . . . . . . . . . . 19
7.2 Setting up the unit .. . . . . . . . . . . 20
7.3 Removing the protective film
from the touch screen .. . . . . . . . 20
7.4 Attaching the stylus .. . . . . . . . . . 20
7.5 Inserting the memory card .. . . . . 20
7.6 Electrical connections .. . . . . . . . 21
7.7 Connecting the device to the
network .. . . . . . . . . . . . . . . . . . . 22
8 Commissioning .. . . . . . . . . . . . . . . . . . 23
8.1 Installing and configuring the unit .. 23
8.2 X-ray unit settings .. . . . . . . . . . . 26
8.3 Acceptance tests .. . . . . . . . . . . 27
Usage
9Operating the touch screen .. . . . . . . . 28
9.1 Navigating .. . . . . . . . . . . . . . . . . 28
9.2 Using menus .. . . . . . . . . . . . . . . 28
9.3 Entering text in the field .. . . . . . . 28
9.4 Calling up messages on the
touch screen .. . . . . . . . . . . . . . . 29
10 Correct use of image plates .. . . . . . . . 29
11 Operation .. . . . . . . . . . . . . . . . . . . . . . 30
11.1 X-ray .. . . . . . . . . . . . . . . . . . . . . 30
11.2 Scanning the image data via a
computer .. . . . . . . . . . . . . . . . . . 34
Contents
9000-608-160/02 2107V004 1
EN

11.3 Scanning image data via the
touch screen on the unit .. . . . . . 37
11.4 Erasing the image plate .. . . . . . . 40
11.5 Switch off the unit. .. . . . . . . . . . 40
12 Cleaning and disinfection .. . . . . . . . . . 41
12.1 Image plate scanner .. . . . . . . . . 41
12.2 Light protection cover .. . . . . . . . 41
12.3 Image plate .. . . . . . . . . . . . . . . . 41
12.4 Foil cassette .. . . . . . . . . . . . . . . 42
12.5 Stylus .. . . . . . . . . . . . . . . . . . . . 42
12.6 Rigid cassette .. . . . . . . . . . . . . . 42
12.7 Foil sleeve .. . . . . . . . . . . . . . . . . 42
13 Maintenance .. . . . . . . . . . . . . . . . . . . . 43
13.1 Recommended maintenance
schedule .. . . . . . . . . . . . . . . . . . 43
Troubleshooting
14 Tips for operators and service techni-
cians .. . . . . . . . . . . . . . . . . . . . . . . . . . 44
14.1 Poor X-ray image .. . . . . . . . . . . 44
14.2 Software error .. . . . . . . . . . . . . . 46
14.3 Fault on the unit .. . . . . . . . . . . . 48
14.4 Error messages on the touch
screen .. . . . . . . . . . . . . . . . . . . . 50
Appendix
15 Settings menu layout .. . . . . . . . . . . . . 52
16 Scanning times .. . . . . . . . . . . . . . . . . . 54
16.1 Intraoral .. . . . . . . . . . . . . . . . . . . 54
16.2 Extraoral .. . . . . . . . . . . . . . . . . . 54
17 File sizes (uncompressed) .. . . . . . . . . 55
17.1 Intraoral .. . . . . . . . . . . . . . . . . . . 55
17.2 Extraoral .. . . . . . . . . . . . . . . . . . 55
Contents
2 9000-608-160/02 2107V004
EN

Important information
1 About this document
These installation and operating instructions rep-
resent part of the unit.
DÜRR MEDICAL will not offer any war-
ranty or accept any liability for the safe
operation and the safe functioning of the
unit if the instructions and information in
these installation and operating instruc-
tions are not complied with.
The German version of the installation and oper-
ating instructions is the original manual. All other
languages are translations of the original manual.
These installation and operating instructions
apply to:
CR 35 VETwin
Order number: 2132-000-61
1.1 Warnings and symbols
Warnings
The warnings in this document are intended to
draw your attention to possible injury to persons
or damage to machinery.
The following warning symbols are used:
General warning symbol
The warnings are structured as follows:
SIGNAL WORD
Description of the type and source of
danger
Here you will find the possible conse-
quences of ignoring the warning
❯Follow these measures to avoid the
danger.
The signal word differentiates between four levels
of danger:
–DANGER
Immediate danger of severe injury or death
–WARNING
Possible danger of severe injury or death
–CAUTION
Risk of minor injuries
–NOTICE
Risk of extensive material/property damage
Other symbols
These symbols are used in the document and on
or in the unit:
Note, e.g. specific instructions regarding
efficient and cost-effective use of the unit.
CE labelling
Manufacturer
Date of manufacture
Dispose of correctly in accordance with
EU Directive 2012/19/EU (WEEE).
Do not reuse
Wear protective gloves.
Disconnect all power from the unit.
Refer to the accompanying electronic
documents.
Observe the operating instructions.
Order number
Serial number
Lot designation
Warning – dangerous high voltage
Warning - laser beam
XX
YY
Lower and upper temperature limits
XX
Upper temperature limit
Important information
9000-608-160/02 2107V004 3
EN

Keep dry
This way up / store and transport in an
upright position
Fragile, handle with care
Keep away from sunlight
n
Stacking limits
DO NOT ROLL
Do not roll
Recycling
ETL Certification
CONFORMS TO UL STD 61010-1
CERTIFIED TO CAN/CSA STD C22:2 NO.
61010-1
1.2 Label
Fig. 1: Laser class 3B
Fig. 2: Warning – laser beams
Information about the laser
source
Danger to components due to
electrostatic discharge (ESD)
1.3 Copyright information
All circuits, processes, names, software pro-
grams and units mentioned in this document are
protected by copyright.
Reprinting of the installation and operating
instructions, or parts thereof, is only permitted
with the written approval of DÜRR MEDICAL.
Important information
4 9000-608-160/02 2107V004
EN

2 Safety
DÜRR MEDICAL has developed and designed
this unit in such a way that it does not pose any
danger to people or property provided it is prop-
erly operated in accordance with the intended
use.
Despite this, the following residual risks can
remain:
– Personal injury due to incorrect use/misuse
– Personal injury due to mechanical effects
– Personal injury due to electric shock
– Personal injury due to radiation
– Personal injury due to fire
– Personal injury due to thermal effects to skin
– Personal injury due to lack of hygiene, e.g.
infection
2.1 Intended use
The unit is intended solely for use in the area of
veterinary medicine for the scanning and pro-
cessing of image data on an image plate.
2.2 Improper use
Any use of this appliance / these appliances
above and beyond that described in the Installa-
tion and Operating Instructions is deemed to be
incorrect usage. The manufacturer cannot be
held liable for any damage resulting from incor-
rect usage. The operator will be held liable and
bears all risks.
WARNING
Risk of explosion due to ignition of
combustible materials
❯Do not operate the unit in any rooms in
which inflammable mixtures may be
present, e.g. in operating theatres.
The device is not suitable for prolonged X-ray
diagnostic monitoring of animals.
The preview of the X-ray image on the touch
screen is not suitable for the purposes of diagno-
sis.
2.3 General safety information
❯Always comply with the specifications of all
guidelines, laws, and other rules and regula-
tions applicable at the site of operation for the
operation of this unit.
❯Check the function and condition of the unit
prior to every use.
❯Do not convert or modify the unit.
❯Comply with the specifications of the Installa-
tion and Operating Instructions.
❯The Installation and Operating Instructions
must be accessible to all operators of the unit
at all times.
2.4 Specialist personnel
Operation
Unit operating personnel must ensure safe and
correct handling based on their training and
knowledge.
❯Instruct or have every user instructed in han-
dling the unit.
Installation and repairs
❯Installation, new adjustments, modifications,
upgrades and repairs must be carried out by
DÜRR MEDICAL or by person(s) specifically
authorised by DÜRR MEDICAL.
2.5 Electrical safety
❯Comply with all the relevant electrical safety
regulations when working on the unit.
❯Never touch the animal or owner and unshiel-
ded plug connections on the unit at the same
time.
❯Replace any damaged cables or plugs immedi-
ately.
2.6 Only use original parts
❯Only use the accessories and optional acces-
sories stated or approved by DÜRR MEDICAL.
❯Only use only original wear parts and replace-
ment parts.
DÜRR NDT accepts no liability for dam-
ages resulting from the use of non-
approved accessories or optional acces-
sories, or from the use of non-original
wear parts or replacement parts.
Important information
9000-608-160/02 2107V004 5
EN

2.7 Transport
The original packaging provides optimum protec-
tion for the unit during transportation.
Where required, original unit packing can be
ordered from DÜRR MEDICAL.
DÜRR MEDICAL cannot be held respon-
sible for any damage to the unit resulting
from transport in unsuitable packaging;
this also applies during the warranty
period.
❯Only transport the unit in its original packaging.
❯Keep the packing materials out of the reach of
children.
❯Do not expose the unit to any strong vibrations
or shocks.
2.8 Disposal
Dispose of correctly in accordance with
EU Directive 2012/19/EU (WEEE).
An overview of the waste keys for DÜRR
MEDICAL products can be found in the
download area at: www.duerr-medical.de
(Document no. GA10100002).
2.9 Protection from threats from
the Internet
The unit is to be connected to a computer that
can be connected to the Internet. Therefore, the
system needs to be protected from threats from
the Internet.
❯Use antivirus software and update it regularly.
Look for evidence of possible virus infection
and, if applicable, check with the antivirus soft-
ware and remove the virus.
❯Perform regular data backups.
❯Restrict access to units to trustworthy users,
e.g. via a user name and password.
❯Make sure that only trustworthy content is
downloaded. Only install software and firmware
updates that have been authenticated by the
manufacturer.
Important information
6 9000-608-160/02 2107V004
EN

Product description
3 Overview
3
4
7
5
9
8
2
1
6
1 CR 35 VETwin Image Plate Scanner
2 Foil cassette, intraoral
3 Image plate intraoral
4 Light protection cover intraoral
5 SDHC memory card
6 Light protection screen
(mounted on device)
7 Network cable
8 Mains cable (country specific)
9 Power supply unit
Product description
9000-608-160/02 2107V004 7
EN

3.1 Scope of delivery
The following items are included in the scope of
delivery (possible variations due to country-spe-
cific requirements and/or import regulations):
CR 35 VETwin
Image Plate Scanner .. . . . . . . . . . . . . 2132-61
– CR 35 Basic unit
– Network cable
– SDHC memory card
– Power supply unit
– Mains cable (country specific)
– Vet-Exam Plus or Vet-Exam Pro Imaging Soft-
ware
– IP Cleaning Wipes
– Installation and operating instructions
– Quick start instructions
3.2 Accessories
The following items are required for operation of
the device, depending on the application:
Image plates
– Image Plate PLUS, size 0
– Image Plate PLUS, size 1
– Image Plate PLUS, size 2
– Image Plate PLUS, size 3
– Image Plate PLUS, size 4
– Image Plate PLUS, size 4C
– Image Plate PLUS, size 5
– Image Plate PLUS, size R3
– Image Plate 18x24
– Image Plate 24x30
– Image Plate 30x40
– Image Plate 35x43
Light protection covers
– Light Protection Cover Plus, size 0
– Light Protection Cover Plus, size 1
– Light Protection Cover Plus, size 2
– Light Protection Cover Plus, size 3 / R3
– Light Protection Cover Plus, size 4
– Light Protection Cover Plus, size 4C
– Light Protection Cover Plus, size 5
3.3 Optional items
The following optional items can be used with the
device:
SDHC memory card .. . . . . . . . . . . 9000-134-18
Bite protector, size 4 (100 pcs) .. . . 2130-074-03
Network cable (5 m) .. . . . . . . . . . 9000-118-036
3.4 Consumables
The following materials are consumed during
operation of the device and must be reordered
separately:
Light protection covers
Light Protection Cover Plus size 0
2 x 3 cm (100 pcs.) .. . . . . . . . . . . 2134-080-00
Light Protection Cover Plus size 1
2 x 4 cm (100 pcs.) .. . . . . . . . . . . 2134-081-00
Light Protection Cover Plus size 2
3 x 4 cm (300 pcs.) .. . . . . . . . . . . 2134-082-00
Light Protection Cover Plus size 3 /
R3
2.7 x 5.4 cm (100 pcs.) .. . . . . . . . . 2134-083-00
Light Protection Cover Plus size 4
5.7 x 7.6 cm (100 pcs.) .. . . . . . . . . 2134-084-00
Light Protection Cover Plus size 4C
4.8 x 5.4 cm (100 pcs.) .. . . . . . . . . 2134108800
Light Protection Cover Plus size 5
5.7 x 9.4 cm (100 pcs.) .. . . . . . . . . 2134-085-00
Cleaning and disinfection
IP cleaning wipes (10 pcs.) .. . . . CCB351A1001
3.5 Wear parts and replacement
parts
Set of light protection brushes .. . 2134-205-00E
Set of vibration reducers .. . . . . . . 2134-305-00E
Toothed belt set .. . . . . . . . . . . . . 2134-315-00E
Set of drive belts (4 pieces) .. . . . . . 2134-993-50
Image plates
Image Plate
18x24 (1 piece) .. . . . . . . . . . . . . . VMIP1824210
Image Plate
24x30 (1 piece) .. . . . . . . . . . . . . . VMIP2430210
Image Plate
30x40 (1 piece) .. . . . . . . . . . . . . . VMIP3040210
Image Plate
35x43 (1 piece) .. . . . . . . . . . . . . . VMIP3543210
Product description
8 9000-608-160/02 2107V004
EN

Intraoral
PLUS image plate, size 0
2 x 3 cm (2 pcs.) .. . . . . . . . . . . . . 2134-040-50
PLUS image plate, size 1
2 x 4 cm (2 pcs.) .. . . . . . . . . . . . . 2134-041-50
PLUS image plate, size 2
3 x 4 cm (4 pcs.) .. . . . . . . . . . . . . 2134-042-50
PLUS image plate, size 3
2.7 x 5.4 cm (2 pcs.) .. . . . . . . . . . 2134-043-50
PLUS image plate, size 4
5.7 x 7.6 cm (1 pcs.) .. . . . . . . . . . 2134-044-50
PLUS image plate, size 4C
4.8 x 5.4 cm (1 pc.) .. . . . . . . . . . . . 2134104800
PLUS image plate, size 5
5.7 x 9.4 cm (1 pcs.) .. . . . . . . . . . 2134-045-50
Plus image plate, size R3
2.2 x 5.4 (2 pcs.) .. . . . . . . . . . . . . . 2134104700
Further image plate formats available on
request
Foil cassettes
Foil cassette 18x24 cm (1 piece) .. . 2132-023-50
Foil cassette 24x30 cm (1 piece) .. . 2132-021-50
Foil cassette 30x40 cm (1 piece) .. . 2132-022-50
Foil cassette 35x43 cm (1 piece) .. . 2132-024-50
Intraoral
Foil cassette size 0
2 x 3 cm (1 piece) .. . . . . . . . . . . . . 2130-010-00
Foil cassette size 1
2 x 4 cm (1 piece) .. . . . . . . . . . . . . 2130-011-00
Foil cassette size 2
3 x 4 cm (1 piece) .. . . . . . . . . . . . . 2130-012-00
Foil cassette size 3
2.7 x 5.4 cm (1 piece) .. . . . . . . . . . 2130-013-00
Foil cassette size 4
5.7 x 7.6 cm (1 piece) .. . . . . . . . . . 2130-014-00
Rigid cassettes
Rigid cassette 18x24 cm (1
piece) .. . . . . . . . . . . . . . . . . . . . . KUNKA182408
Rigid cassette 24x30 cm (1
piece) .. . . . . . . . . . . . . . . . . . . . . KUNKA243007
Rigid cassette 30x40 cm (1
piece) .. . . . . . . . . . . . . . . . . . . . . KUNKA304010
Rigid cassette 35x43 cm (1
piece) .. . . . . . . . . . . . . . . . . . . . . KUNKA354307
Foil sleeves
Foil sleeve 18x24 (1 piece) .. . . . . NACS1824107
Foil sleeve 24x30 (4 piece) .. . . . . . 2134-024-00
Foil sleeve 30x40 (4 piece) .. . . . . . 2134-033-00
Foil sleeve 35x43 (4 piece) .. . . . . . 2134-034-00
Further information about the replace-
ment parts on demand
Product description
9000-608-160/02 2107V004 9
EN

4 Technical data
4.1 Image plate scanner
Electrical data for the unit
Voltage V DC 24
Max. current consumption A 5
Output W < 120
Electrical data – power supply unit
Voltage V AC 100 - 240
Frequency Hz 50 - 60
Protection class I
Type of protection IP20
Output W < 140
Max. current consumption A 2
Classification
EMC Directive (2014/30/EU)
RoHS Directive (2011/65/EU)
Laser class (unit)
In accordance with IEC 60825-1:2014
1
Laser source
Laser class
in accordance with EN 60825-1:1994-03
+
A1:2002-07 + A2:2001-03
3B
Wavelength lnm 660
Output mW 80
Noise level
Standby dB(A) 0
Ready to scan dB(A) approx. 37
During scanning dB(A) approx. 55
General technical data
Dimensions (W x H x D) cm 37 x 40 x 47
in 14.3 x 15.7 x 18.5
Weight kg approx. 17.5
lb approx. 38.6
Max. feeding width for image plates cm 35.4
in 13.9
Product description
10 9000-608-160/02 2107V004
EN

General technical data
Duty cycle S2 (in accordance with VDE
0530-1)
min 60
Duty cycle S6 (in accordance with VDE
0530-1)
% 70
Degree of soiling 2
Pixel size (selectable) μm 12.5 - 130
Max. theoretical resolution Line
pairs/mm
(Lp/mm)
approx. 20
Network connection
LAN technology Ethernet
Standard IEEE 802.3u
Data rate Mbit/s 100
Connector RJ45
Type of connection Auto MDI-X
Cable type ³CAT5
WLAN connection
WLAN technology IEEE 802.11b/g
Encryption WPA, WPA2
Memory card
Type SDHC
Maximum memory capacity GB 32
File system FAT32
Performance class Class ³4
Ambient conditions during operation
Temperature °C +10 to +35
°F +50 to +95
Relative humidity % 20 - 90
Air pressure hPa 750 - 1060
Ambient conditions during storage and transport
Temperature °C -20 to 60
°F -4 to +140
Relative humidity % 10 - 95
Air pressure hPa 750 - 1060
Product description
9000-608-160/02 2107V004 11
EN

4.2 Image plate
Ambient conditions during operation
Temperature °C 18 - 45
°F 64 - 113
Relative humidity % < 80
Ambient conditions during storage and transport
Temperature °C < 33
°F < 91
Relative humidity % < 80
Dimensions of intraoral image plates
Size 0 mm 22 x 35
in 0.87 x 1.38
Size 1 mm 24 x 40
in 0.94 x 1.57
Size 2 mm 31 x 41
in 1.22 x 1.61
Size 3 mm 27 x 54
in 1.06 x 2.13
Size 4 mm 57 x 76
in 2.24 x 2.99
Size 4C mm 48 x 54
in 1.89 x 2.13
Size 5 mm 57 x 92
in 2.24 x 3.62
Size R3 mm 22 x 54
in 0.87 x 2.13
Dimensions of image plates
18 x 24 mm 178 x 227
in 7.01 x 8.94
24 x 30 mm 238 x 298
in 9.37 x 11.73
30 x 40 mm 298 x 398
in 11.73 x 15.67
35 x 43 mm 354 x 430
in 13.94 x 16.93
Product description
12 9000-608-160/02 2107V004
EN

4.3 Type plate
The type plate is located on the rear side of the
foot.
4.4 Evaluation of conformity
This device has been subjected to conformity
acceptance testing in accordance with the cur-
rent relevant European Union guidelines. This
equipment conforms to all relevant requirements.
ETL approval
This Class A device complies with Canadian
ICES-003.
The equipment has been tested and found to
comply with the limits for a class A digital device,
pursuant to Part 15 of the FCC rules. These limits
are designed to provide reasonable protection
against harmful interference when the equipment
is operated in a commercial environment. This
unit generates, uses and emits radio frequency
energy. If the device is not set up and operated
in accordance with the installation and operating
instructions, this can lead to interference in radio
communications. Operation of the equipment in
a residential area may cause malfunctions to
occur on the device. The operator will be
required to remedy such malfunctions or interfer-
ence at his own expense.
FDA registration
Complies with FDA performance standards for
laser products except for deviations pursuant to
Laser Notice No. 50, June 2007.
Product description
9000-608-160/02 2107V004 13
EN

4.5 Declaration of conformity
Name of manufacturer: DÜRR NDT GmbH & Co. KG
Address of manufacturer: Höpfigheimer Straße 22
74321 Bietigheim-Bissingen
Germany
Name of product: CR 35
Image plate scanners
We hereby declare that the above product meets all applicable requirements of the directives listed
below:
– Electromagnetic Compatibility (EMC) Directive 2014/30/EU in its current version.
– Directive 2011/65/EU on the restriction of the use of certain hazardous substances in electrical and
electronic equipment in its current version.
O. Ruzek O. Lange on behalf of Duerr Dental
CEO Head of Quality Management
Product description
14 9000-608-160/02 2107V004
EN

5 Operation
5.1 Image plate scanner
4
2
3
5
6
1
7
1 Stylus
2 + 3 Entry slots
4 User interfaces
5 + 6 Entry slots
7 Memory card slot
The image plate scanner is used to read image
data stored on the image plate.
The device can be used in two different ways: via
the imaging software on a PC or directly via the
touch screen on the unit.
The transport mechanism guides the image plate
through the device. The image plate is read using
a laser inside the scanner unit. The scanned data
is converted into a digital image.
If a scanning task is started via the imaging soft-
ware, the image is automatically transmitted to
the computer.
If a scanning task is started via the touch screen,
the image is saved to the memory card and then
needs to be transferred to the computer.
After scanning, the image plate runs through the
erasure unit. Image data still held on the image
plate is erased with the aid of bright light.
The image plate is then ejected for re-use.
The unit can scan up to four image plates
(depending on the sizes) simultaneously with the
same resolution.
Operating elements
2
1
1 Touch screen
2 On / off switch
The touch screen allows the unit to be operated
when it is not connected to a computer. Instruc-
tions can be entered on the touch screen either
with the tip of a finger or the stylus.
The Help button can be used to open a help
page for the relevant screen. The Messages but-
ton can be used to recall current messages.
Product description
9000-608-160/02 2107V004 15
EN

Connections
The connections are located on the rear of the
unit.
1234
1 Reset button
2 Connection for power supply unit
3 AUX connection for diagnostic units
4 Network connection with status LED
Exposure recognition
When the exposure recognition is switched on,
then the device will detect whether an image
plate is exposed or not on insertion. When an
exposed image plate is scanned then an X-ray
image will be displayed. When an unexposed
image plate is scanned then an empty image
plate will be displayed. No preview image is dis-
played on the touch screen
When the exposure recognition is switched off
and an unexposed image plate is scanned then
the device will not display anything on the touch
screen or in the software.
DualFoc
The DualFoc technology of the device allows the
size of the laser spot to be set. This provides X-
ray images with optimal signal/noise ratio and
optimally adapted resolution.
The predefined scanning modes allow the appro-
priate scanning mode to be selected for the par-
ticular application, depending on the image plate
used.
For example with the intraoral image plates
(blue), the "VET Dental" scanning mode supports
the read-out for maximum detailing with the high
resolution of 12.5 µm laser spots.
On the other hand, for an abdomen examination,
the "VET Standard" scanning mode is used with
an extraoral image plate (white) and the setting
for the large laser spot of 50 µm is selected in
order to produce a brilliant, low noise image.
Product description
16 9000-608-160/02 2107V004
EN

5.2 Image plate
The image plate stores X-ray energy, which is re-
emitted in the form of light after excitation via the
laser. This light is then converted to image infor-
mation in the image plate scanner.
The image plate has an active side and an inac-
tive side. The image plate must always be
exposed on the active side.
When used properly, image plates can be
exposed, read and erased several hundred times
provided there is no mechanical damage. The
image plate must be replaced if there are any
signs of damage, e.g. if the protective layer is
damaged or there are visible scratches that could
interfere with the diagnosis.
Intraoral
2
1
1Inactive side Black, with the size and
manufacturer information
printed on it
2 Active side Light blue, with position-
ing aid 3
Positioning aid 3is visible on the X-ray image and
makes orientation easier during diagnosis.
Extraoral
1
2
1 Inactive side black, with manufactur-
er's information printed
on it
2 Active side White
5.3 Light protection cover
The light protection cover protects the image
plate against light.
5.4 Flexible foil cassette
The flexible foil cassette has several protection
features for extraoral image plates:
– Protection against sunlight and UV light, and
therefore protection against accidental erasure
– Protection against mechanical damage
The flexible foil cassette can be used in non-dirty
environments.
Product description
9000-608-160/02 2107V004 17
EN