Dosimax plus A HV

Dosemeter

User Manual
2
 Preface

This operating manual is an integral component of the dose ­ surfaces ­ product measuring system
Dosimax® plus and should always be kept in the proximity of the actual measuring system. This
®
operating manual is needed, in order to ensure the correct function and operation of the Dosimax
®
plus system. The Dosimax plus system together with its accessories may be used for no other
purposes other than those specified in this operating manual.

The use of the Dosimax® plus and every other system described in this document, the resulting data,
as well as the substantiation of the data before use in a clinical environment, is the sole responsibility
of the user. Iba Dosimetry accepts no liability for personal injury or damage to devices due to faulty
operation, neglect of the danger warnings in this operating manual or local health and safety
regulations. No part of this operating manual may be translated or be reproduced in any way without
the express written consent of the company Iba Dosimetry.

The user must treat this documentation like any other copyright protected material. Particularly, if parts
of the enclosed documentation are present in electronic form, these may not be modified in any way.
Iba Dosimetry owns all copyrights in the enclosed documentation (both in electronic and written form).
Several key functions of the Dosimax® plus and its associated components are protected by
international patents.

Manufacturer : Iba Dosimetry GmbH

Adress : Bahnhofstraße 5, DE­90592 Schwarzenbruck
Tax Nr. : 241/137/21452
VAT­Nr. : DE132815519
WEEE­Reg.­Nr. : DE 65960409

Copyright © 2006 by Iba Dosimetry GmbH.

All other Brands, Trademarks and Trade Names mentioned in this documentation are the property of
the applicable manufacturers and companies. IBA DOSIMETRY GmbH renounces all claims of
possession to rights in Brands, Trademarks and Trade Names mentioned in this documentation which
are not their property.

Note:
The use of the device as agreed is fixed obviously on the following pages. Every use differing from it
leads to a risk transition on the user.

0124

­3­
Table of Contents
Table of Contents ...................................................................................................................4
1.1. Short description of the DOSIMAX plus....................................................................5
Important Notice .................................................................................................................6
1.2. Statement of intended use........................................................................................7
1.3. User Restrictions......................................................................................................7
1.4. Environmental Conditions.........................................................................................8
2 System components........................................................................................................9
2.1. Standard components ..............................................................................................9
Accessories (optional).......................................................................................................12
3 Operating instructions ...................................................................................................13
3.1. ON/OFF key ...........................................................................................................13
3.2. PARAMETER keys.................................................................................................13
3.2.1. DOSE key .......................................................................................................13
3.2.2. DOSE RATE key.............................................................................................13
3.2.3. TIME key.........................................................................................................14
4 Measuring Setup ...........................................................................................................15
4.1. General procedure .................................................................................................15
4.2. Practical hints.........................................................................................................16
5 Measurements ..............................................................................................................17
5.1. Dose measurement ................................................................................................17
6 Changing the batteries ..................................................................................................19
7 Technical data...............................................................................................................20
7.1. Basic instrument.....................................................................................................20
7.2. Detector RQA.........................................................................................................21
7.3. Detector RQM (separate detector for use in mammographic installations) .............23
7.4. DCT10­RS chamber (separate ionization chamber for measuring at CT scanners)24
7.5. DC300­chamber (ionization chamber for conventional radiation and mammography
devices) ............................................................................................................................26
Active Volume: 2.98 cm³ ...............................................................................................26
8 Quality Assurance Tests................................................................................................27
9 Troubleshooting – Error indications ...............................................................................29
10 Warranty .......................................................................................................................30
10.1. General...............................................................................................................30
10.2. Warranty period ..................................................................................................30
10.3. Limitations ..........................................................................................................30
10.4. Consequential damage or personal injury ...........................................................31
11 Recycling ......................................................................................................................31

­4­
 Introduction

1.1. Short description of the DOSIMAX plus

The DOSIMAX plus A dosemeter is a fully automatic precision instrument for measuring
dose, dose rate and exposure time simultaneously. Semi­conductor detectors are used
which offer, in comparison to ionization chambers, a number of well­known advantages e.g.
they are unaffected by air pressure and temperature. The ionization current of the semi­
conductor detector is measured, converted into the dosimetrical unit Gray (Gy) and then
shown in the display.

The DOSIMAX plus A has the following features:

· Automatic sensitivity change­over between radiography and fluoroscopy

· Automatic reset
· Easy parameter selection by using the corresponding key
· Direct readout of measured values
· Auto power­off after a period of 10 minutes when no user interaction or
measuring takes place.

The following detectors can be used in connection with the DOSIMAX plus A:

· Detector RQA, a separate external detector used in conventional radiology

· Detector RQM, a separate external detector used in mammographic radiology
· DCT10­ RS, an Ionizationchamber used in CT radiology
· DC 300, an Ionizationchamber used in conventional radiology and
mammographic radiology

The following radiation qualities can be calibrated for the RQA detector in conventional
radiography (50 ­150 kV) in the Dosimax plus A:

Filtration
Beam quality voltage [kV]
[mm Al]
RQR 5 70 2,5
RQA 5 70 23,5

­5­
For the RQM detector for dose measuring in the Mammografie (25 kV ­ 35 kV) the following
radiation qualities are calibrated:

Beam quality voltage [kV] Filtration

RQR­M2 28 30 µm Mo

For the ionization chamber DCT10­RS for dose length measuring in CT qualities (100 kV ­
150 kV) the following radiation qualities are calibrated:

Beam quality voltage [kV] Filtration

RQR­8 100 2,5 mm Al
T140 140 8 mm Al

For the ionization chamber DC300 for dose measuring in the Mammografie (25 kV ­ 35 kV)
and conventional radiography (50 ­150 kV) the following radiation qualities can be calibrated:

Beam quality voltage [kV] Filtration

RQR 5 70 2,5 mmAl
RQA 5 70 23,5 mmAl
RQR­M3 30 30 µm Mo
RQA­M3 30 30 µm Mo + 2 mmAl

Important Notice

This manual contains information necessary to use the DOSIMAX plus A and associated
detector(s) safely and effectively.

The DOSIMAX plus A should not be used until the operator is familiar with the contents of
this manual and particularly the sections prefixed with "Important", "Caution" or "Warning "
printed in bold text.

­6­
1.2. Statement of intended use

The DOSIMAX plus A is intended to be used to provide quality assurance in the

measurement of the beam intensity of X­ray installations.

1.3. User Restrictions

The DOSIMAX plus A is a medical device compliant with the German Medicine Product Law
and as such must, in Germany, undergo a two yearly check of it’s accuracy and general
condition. With this in mind please ensure that all local regulations and laws applicable to the
use of a product of this type in your country are also adhered to.

Important ­ Incident reporting:

If the system is involved or associated directly or indirectly with a hazardous incident

it should be withdrawn from service immediately and the details reported to the
manufacturer.

A copy of this manual is supplied with each DOSIMAXplus system to ensure correct
operation. It must not be copied in part or in whole, or used for any other purpose
without the written permission of the manufacturer.

Several features of the DOSIMAX plus and its component accessories are subject to
patent applications.

Modifications to the product or the content of this manual will invalidate the product
warranty and may compromise safe operation. Do not therefore, under any
circumstances, make any changes to the product or it’s component accessories.

Every effort has been made to ensure that this manual is sufficiently accurate for its
intended purpose. The manufacturer would appreciate being informed of possible
errors and suggestions for improvements.

­7­
1.4. Environmental Conditions

Allowed Environmental Conditions

Working temperature range: 15 °C ­ 35 °C

Humidity: < 80 %
Pressure: 700 hPa – 1060 hPa

Reference Range (Factory Calibration)

Temperature: 20 C°
Humidity: 20 % ­ 75 %, ≤ 20 g/m3
Pressure: 800 ­ 1060 hPa

­8­
 2 System components

2.1. Standard components

The DOSIMAX plus measuring system consists of a basic measuring and display unit and
one or two detectors:

Figure 1: DOSIMAX plus – basic instrument

Figure 2: Detector RQA. A flexible sensor for radiographic measurements.

( select an RQA or RQM detector in this set)

­9­
Figure 3: Detector RQM. A flexible detector, for mammographic measurements.

( select an RQA or RQM detector in this set)

Figure 4: DCT­10 Ionisation chamber for measuring at CT facilities

­ 10 ­
Figure 5: DC300 ionization chamber for measuring in the mammography and
conventional radiography

­ 11 ­
 Accessories (optional)

Figure 3: Detector extension cable, 8 m

Figure 4: Cartridge adapter for the RQA detector

The dosemeter – detector combination can be used with different types of test tools, e.g.
the detector RQM with the mammography test tool MAMMO­152.

­ 12 ­
 3 Operating instructions

The basic unit has four keys, one ON/OFF key and three parameter keys.

3.1. ON/OFF key

The instrument is activated by pressing the ON/OFF key.

If the DOSIMAX plus A is not used for longer than 10 minutes (no radiation detection or
pressing of any key), the device switches itself off automatically (battery saving function).
The display lighting switches itself off after 3 minutes. It is activated again either after
radiation detection or by pressing a key.

3.2. PARAMETER keys

3.2.1. DOSE key

The dose key is used in order to indicate the dose value of the preceding exposure in the
display (Figure 2).

Figure 2

3.2.2. DOSE RATE key

The dose rate key is used in order to indicate the dose rate of the preceding exposure in
the display (Figure 3).

Figure 3

­ 13 ­
3.2.3. TIME key

The time key is used in order to indicate the exposure time of the preceding exposure in the
display (Figure 4).

Figure 4

­ 14 ­
 4 Measuring Setup

4.1. General procedure

The DOSIMAX plus A was developed to measure dose, dose rate and exposure time
simultaneoulsly, fast and simply, but with the highest precision.

The measuring setup is very easy:

· Position the chosen detector in the field of radiation (central beam) and make sure
that the marked side of the detector is facing towards the X­ray tube.

· Switch on the DOSIMAX plus A by pressing the ON/Off key. Straight away a display
test (the “IBA DOSIMETRY” logo appears first) is started. The following display
messages informs the user about the on board software version and the serial
number of the basic DOSIMAX plus A unit. Additionally, if the Instrument is
programmed to use more than one detector, the following screen appears:

· You can switch to another calibrated sensor with the TIME­button. When the desired
sensor is displayed please select it by pressing the DOSE­button.
· If the selected sensortype is an ionization­chamber (i.e. DCT10­RS or DC300) then
the following screen appears:

· If you want to switch on the highvoltage then confirm it with the DOSERATE­button
otherwise select a another sensor by switching off.
· The high voltage becomes started and stabilized (30 sec.)

­ 15 ­
 · When the “DOSE” indication (this is the default message) appears.
· The symbol (flash) shows that the high voltage (400 V) is on now.

· The instrument is ready to start taking measurements.

· Start an exposure and:
o Select with the “DOSE” key the dose indication or
o Select with the “DOSERATE” key the dose rate indication or
o Select with the “TIME” key the time indication
and read off the measured values.

After each exposure the chosen parameter and its corresponding unit of measurement is
clearly visible in the display.

During each new exposure an automatic RESET of the device takes place.

4.2. Practical hints

Please note that an accurate measurement result pre­supposes that the entire detector
surface is irradiated (except DCT10­RS). The active detector surfaces can be made
particularly small by the use of high resolution silicon semiconductors.

Due to the high sensitivity of the detectors, it is possible that a triggering can take place
without the effect of radiation (e.g. through a shifting current value in the cable when
mechanicaly moved). Therefore neither the detector/s or the measuring cable should be

­ 16 ­
 moved, or suspended in a way that a mechanical influence can occur, during the switching
on phase or during the taking of measurements.

5 Measurements

5.1. Dose measurement

The dose measurement in the radiographic mode is started as soon as a trigger threshold is
exceeded. On the display the dose value appears (Figure 5). An “M” in the top line of the
display indicates that a signal has been recognized. The measurement is terminated after a
time interval of 2 s without radiation detection run off.

Figure 5

After measurement the dose value is indicated (Figure 6).

Figure 6

By pressing the DOSERATE­Button, the dose rate and the time value is indicated
(Figure 7).
­ 17 ­
 Figure 7

By pressing the TIME­Button, the time value is indicated

(Figure 8).

Figure 8

­ 18 ­
6 Changing the batteries

By means of the battery symbol the battery status can be verified.

If the capacity of the batteries is too low, measurements are no longer possible.

If the battery symbol flashes , the batteries must be changed immediately.

Commercial AA batteries (Mignon) can be used, whereas alkaline batteries LR 6 are
preferred because a longer function period is possible. In order to change the batteries, you
must carefully slide the battery compartment lid downwards (Figure 9).

Figure 9

Exchange the batteries and close the lid again.

The use of rechargable batteries (Accumulators) is not recommended.

Note: If you do not intend to use the DOSIMAX plus A for a longer period of time, please
remove the batteries before storage.

­ 19 ­
 7 Technical data

7.1. Basic instrument

EMC testing: according IEC 801­2, ­3 and EN 55011

Wave form: 1­pulse up to middle frequency / high frequency
generators

Exposure time: 1 ms to 19999 s

Reset: automatic
Switching Off: automatically after 10 minutes of inactivity or by use of
the Off key.

Interface: Bluetooth
Power supply: 4 Mignon batteries(AA) 1,5V each or alkaline (LR6)
Working time: 15 hours (alkaline batteries)
Display: LCD­DOT­Matrix, 5 Digits and units
Weight: 280 g / 0.44 lb (basic equipment without batteries)
290 g / 0.64 lb (basic equipment with batteries)

Size (H x W x L):
Dosimeter: 35 x 90 x 145 mm, (1.4’ x 3.5’ x 5.8’)

Operating temperature: 15 to 35 °C (59 to 95 °F), Storage: 0 bis + 60 °C (32 to

140 ° F)

Relative air humidity: < 80 %

­ 20 ­
7.2. Detector RQA

Type of detector: Silicon photodiode (PIN)

Measurement principle: Ionization current in the semiconductor detector
Detector patch cord: Triaxial plug type Lemosa, size 0
Nominal measuring range for 50­150 kV tube voltage in the unattenuated
diagnostic beam qualities: useful beam (RQR 3 – RQR 10, acc. DIN EN
61267)

50­150 kV tube voltage in the attenuated useful

beam (RQA 3 ­ RQA 10, acc. DIN EN 61267)

Calibration factor: 0.0188 mGy/nC (70 kV, 2.5 mm Al)

0.0174 mGy/nC (70 kV, 25 mm Al)

Response: 53.2 nC/mGy (70kV, 2.5 mmAl)

57.5 nC/mGy (70kV, 25 mmAl)

Dose measuring range: 200 nGy bis 9999 mGy

Dose rate measuring range: 50 nGy/s bis 120 mGy/s
Measurement uncertainty: < 5 % (by a minimal dose rate of 50 nGy/s)
Weight: 85 g (0.18 lb)
Size (L x W x H): 45 x 20 x 8 mm (1.7’ x 0.78’ x 0.31’)

Maximum cable length: 10 m (394’)

Calibration reference point: 70 kV, 2.5 mm Al, 1 m distance (RQR5)

­ 21 ­
 1. HVL Filtration
Beam quality voltage [kV] Cq
[mm Al] [mm Al]
RQR 3 50 1,8 2.5 1.03
RQR 4 60 2,0 2.5 1.01
RQR 5 70 2,5 2.5 1.00
RQR 6 80 2,9 2.5 0.99
RQR 7 90 3,3 2.5 0.99
RQR 8 100 3,7 2.5 0.99
RQR 9 120 4,5 2.5 0.99
RQR10

RQR­Qualitäten

1,05

1,03

1,01

0,99

0,97

0,95
RQR 3 RQR 4 RQR 5 RQR 6 RQR 7 RQR 8 RQR 9

1. FWHM Filtering [mm

Beam quality voltage [kV] Cq
[mm Al] Al]
RQA 3 50 3,8 2,5 + 10 0,98
RQA 4 60 5,4 2,5 + 16 0,99
RQA 5 70 6,8 2,5 + 21 1,00
RQA 6 80 8,2 2,5 + 26 0,94
RQA 7 90 9,2 2,5 + 30 0,94
RQA 8 100 10,1 2,5 + 34 0,94
RQA 9 120 11,6 2,5 + 40 0,95
RQA10

­ 22 ­
 RQA­Qualitäten

1,05

1,03

1,01

0,99

0,97

0,95
RQA 3 RQA 4 RQA 5 RQA 6 RQA 7 RQA 8 RQA 9

7.3. Detector RQM (separate detector for use in mammographic installations)

Type of detector: Silicon photodiode (PIN)

Measurement principle: Ionization current in the semiconductor detector
Detector patch cord: Triaxial plug type Lemosa, size 0
Nominal measuring range for 25–35 kV tube voltage in the unattenuated
diagnostic beam qualities: useful beam (RQR­M1 – RQR­M4, acc. DIN EN
61267)
25–35 kV tube voltage in the attenuated useful
beam (RQA­M1 – RQA­M4, acc. DIN EN 61267)

Calibration factor: 0.070 mGy/nC (30 kV, 30 µm Mo)

Response: 14.3 nC/mGy (30 kV, 30 µm Mo)
Dose measuring range: 1,5 µGy to 9999 mGy
Dose rate measuring range: 1,5 µGy/s to 300 mGy/s
Measurement uncertainty: < 5 % (by a minimal dose rate of 1,5µGy/s)
Weight: 85 g (0.18 lb)
Size (L x W x H): 45 x 20 x 8 mm (1.7’ x 0.78’ x 0.31’)
Maximum cable length: 10 m (394’)
Calibration reference point: 28 kV,30µmMo, 0,5m distance (RQR­M2)

Beam quality voltage [kV] 1. HVL Filtration Cq

­ 23 ­
 [mm Al] [mm Al]
RQR­M1 25 0.28 30 1.04
RQR­M2 28 0.31 30 1.01
RQR­M3 30 0.33 30 1.00
RQR­M4 35 0.36 30 0.98
RQA­M1 25 0.56 30 + 2mmAl 0.95
RQA­M2 28 0.60 30 + 2mmAl 0.98
RQA­M3 30 0.62 30 + 2mmAl 1.00
RQA­M4 35 0.68 30 + 2mmAl 1.05

RQM­Qualitäten

1,05

1,03

1,01

0,99

0,97

0,95
RQR­M1 RQR­M2 RQR­M3 RQR­M4 RQA­M1 RQA­M2 RQA­M3 RQA­M4

7.4. DCT10­RS chamber (separate ionization chamber for measuring at CT scanners)

Features:
­ ionization chamber
­ homogeneous response throughout the entire active chamber length
­ guarded
Material:
­ outer electrode reinforced carbon fiber Expoxy (CFK)
­ inner electrode reinforced carbon fiber Expoxy (CFK)
­ plug type triaxial, BNC banana or lemosa
­ connection cable approx. 1.2 m flexible, Low noise

Measures:
­ active volume 4.9 cm3
­ 24 ­
 ­ active length 100 mm
­ inside diameter of the
outer electrode 8,0 mm
­ diameter of the inner
electrode 1,0 mm

Operated date:
­ leakage < +/­4x10­15 A
­ beam quality 100 KV – 150 KV
(field of application)
­ calibration factor (typ.) ND,K= 70 mGy*cm/nC
(120 KV / HWD 4.05 mm Al)

Typical correction factors:

Voltage Filtration Filtration Filtration

[kV] [8 mm Al] [12 mm Al] [4 mm Al+0,2mm Cu]
80 1,05 0,99 0,98
125 1,00 0,96 0,96
140 1,00 0,98 0,98

CT­Qualitäten

1,05

1,03

1,01
kQ

0,99

0,97

0,95
80 125 140
Spannung

­ 25 ­
7.5. DC300­chamber (ionization chamber for conventional radiation and
mammography devices)
Technical data:
Sensitivity (typical): 106 nC/Gy (70 kV, 2,5 mm Al)
Calibration factor (typical): 9,43 mGy/nC (70 kV, 2,5 mm Al)
Cylinder diameter: 10 mm
Cylinder Length: 36 mm
Active Volume: 2.98 cm³
Chamber wall: c 552 air aquivalent
Type of Connector: Lemosa­Plug, Size 0
Leakage: <10­14 A

1.HVL Filtration
Beam quality Voltage [kV] kq
[mm Al] [mm Al]
RQR 3 50 1,8 2,5 1,001
RQR 4 60 2,0 2,5 1,002
RQR 5 70 2,5 2,5 1,000
RQR 6 80 2,9 2,5 1,001
RQR 7 90 3,3 2,5 1,002
RQR 8 100 3,7 2,5 1,005
RQR 9 120 4,5 2,5 1,009

RQR­Qualitäten

1,050

1,030

1,010

0,990

0,970

0,950
RQR 3 RQR 4 RQR 5 RQR 6 RQR 7 RQR 8 RQR 9

­ 26 ­
 1.HVL Filtration
Beam quality Voltage [kV] kq
[mm Al] [mm Al]
RQA 3 50 3,8 2,5 + 10 0,987
RQA 4 60 5,4 2,5 + 16 0,987
RQA 5 70 6,8 2,5 + 21 1,000
RQA 6 80 8,2 2,5 + 26 1,008
RQA 7 90 9,2 2,5 + 30 1,011
RQA 8 100 10,1 2,5 + 34 1,025
RQA 9 120 11,6 2,5 + 40 1,035

RQA­Qualitäten

1,050

1,030

1,010

0,990

0,970

0,950
RQA 3 RQA 4 RQA 5 RQA 6 RQA 7 RQA 8 RQA 9

8 Quality Assurance Tests

Even if a self check of the DOSIMAX plus A dosemeter ­ detector combination is done after
every switch­on, QA tests should be carried out at regular intervals in order to verify the
general functionality, safety and general condition of the dosemeter, the detector(s) and all
accessories. Please observe the environmental reference conditions stated below.

Suggested time table for QA tests

Type of test Frequency Tolerance

­ 27 ­
Calibration Every 5 years +/­ 5 %

Dosemeter is free of damage Before every

together with exposed cables / messuring
detector(s) session

Remarks:

The named quality assurance tests are recommondations only.

International standards and national laws must be observed.

­ 28 ­
9 Troubleshooting – Error indications

Generally, the DOSIMAX plus A has been designed to have a long reliable life. If a problem
is noticed with a measuring system, it may not just be caused by the detector assembly, but
also by the display, processor, power supply or interconnecting cables.

The following error indications can appear on the display if the measuring conditions were
incorrect:

*OVERFLOW* : High dose rate. Reduce mA, or increase the focus detector
distance.

* ERROR *
HV TOO LOW
CHECK INPUT AND
RESTART UNIT!: short circuit on the input socket (cable or chamber failure)
Please contact our service department

Problems other than those indicated above will probably require fault correction by the
manufacturer. Please report the problem to your local supplier who will arrange for the
product to be returned for repair.

­ 29 ­
 10 Warranty

10.1. General
Iba Dosimetry warrants the DOSIMAX plus A and associated accessories to be free of
defects within the warranty period. In case of a defect, Iba Dosimetry will correct the fault or
replace the product at no cost for the owner. In the case of a fault, the owner should first
report the problem to the supplier, or the manufacturer, Iba Dosimetry.
The following information must be given in order to claim under warranty:
v The nature of the problem
v The date the product was purchased
v The model number of the item which is faulty
v The serial number of the item which is faulty

The cost of packing and shipping goods for return shall be the responsibility of the owner
unless otherwise agreed in writing prior to shipment. Any damage caused to returned goods
during shipment shall be the responsibility of the owner. On receipt of the goods the
manufacturer will carry out an inspection to confirm that the problem is covered by this
warranty. In cases were the problem is not covered by warranty, the owner will receive a
quotation for repair. All warranty work will be completed within twenty one days of receipt of
the goods, or the item will be replaced.
The terms of this warranty do not affect the owners statutory rights under applicable national
or local legislation or claims against a local supplier arising from a sale or purchase contract.
Claims of this nature should be addressed to the supplier.

10.2. Warranty period

The normal warranty period for all items is 12 months from the date of purchase;
other periods must be agreed in the written form.

10.3. Limitations
The warranty does not cover the following.
v Periodic checks, calibrations or preventive maintenance.
v Defects with equipment which has been modified without the
written approval of the manufacturer.
v Damage resulting from normal wear and tear.
v Damage resulting from improper use or handling including, but not
limited to, the product being dropped or incorrectly installed.

­ 30 ­
 v Accidents or disasters which are beyond the control of the
manufacturer, including, but not limited to lightning, fire, public
disturbances and improper ventilation.

10.4. Consequential damage or personal injury

The manufacturer will not accept liability for consequential damage or personal injury
resulting from the use of the product, whether fully functional or faulty, until such time as
regulatory and legal authorities have established negligence on the part of the manufacturer.

11 Recycling
This measuring device and its components contain electronic components, liquid crystal
displays and batteries.
None of the parts mentioned may be disposed of by way of the general house or hospital
waste disposal system. If you have no facility to convert the device to electronic waste at the
end of it’s life cycle, please return it to IBA DOSIMETRY. We will carry out an
environmentaly correct recycling.

Note: It is the users responsibility to follow the guidance given in this user manual
together with established professional practice to ensure that the product is
in a usable condition and is being used correctly.

Subject to change. June 2006 VD UM DOSIMAX plus A HV 001

IBA Dosimetry GmbH

Bahnhofstraße 5 | 90592 Schwarzenbruck | Germany | Tel.: +49 9128 607 14 | Fax: +49 9128 607 814

www.iba­dosimetry.com | info@iba­dosimetry.com

­ 31 ­