Remote Diagnostic Technologies 0002 Tempus 2000 Patient Monitor User Manual CUD 34 Revision 00 Tempus 2000

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Date Submitted	2004-01-20 00:00:00
Date Available	2004-01-20 00:00:00
Creation Date	2003-12-08 10:41:42
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Document Title	CUD-34 Revision 00 Tempus 2000 User Manual.doc
Document Creator	CUD-34 Revision 00 Tempus 2000 User Manual.doc - Microsoft Word
Document Author:	channan

User/Operator Manual
Tempus 2000
Maintenance, Servicing and Troubleshooting
7.1 General
The Tempus 2000 is designed to be as maintenance-free as possible. The only
user-replaceable and user-serviceable parts in the Tempus 2000 are those listed
in this section of the manual.
7.2 Battery Removal and Replacement
Press the
button in the Advanced Help Menu in order to bring up the
helpscreen for this activity.
Follow the instructions given in the helpscreen to complete this activity.
7.2.1 Removing the Battery
WARNING
Do not short-circuit the terminals of any battery. A short circuit can occur if
the battery terminals come into contact with any metal or other electrically
conductive object. The battery may be irreversibly damaged if it is shortcircuited.
IMPORTANT
Before removing the battery you must switch off the Tempus 2000 by
pressing and holding the power button for two seconds.
Remember that the battery cannot be removed until the red lamp on the front
panel has gone out.
7.2.2 Charging Batteries
For full details on charging the rechargeable battery, please refer to the Tempus
2000 Battery Charger User/Operator Manual (part number 41-0003).
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To charge the RDT rechargeable batteries, simply place the battery into the
opening of the charger. The battery can only be inserted in the correct orientation
and will easily drop into place if the orientation is correct.
Ensure that the charger is connected to the associated power supply and that the
power supply is connected to a mains supply. The mains supply that is supplied
with the charger is approved for use in most areas including North America and
Europe. It is supplied with a cord that is appropriate and approved for use in the
relevant market and it must be ensured that this cord is always used. If the cord is
damaged or needs replacing, it must be replaced with another of the same type
and rating.
Connect the power supply to the charger box by pushing the low vo ltage jack
socket on the end of the power supply output lead into the receptacle on the
charger.
NOTE
Batteries cannot be charged on board aircraft but may be charged in land or
sea based locations (where no other restrictions apply e.g. in hazardous
locations).
Note that when the battery is first inserted into the charger, the “Charged” and
“Charging” LEDs may flash intermittently for a short period of time (20 seconds to
4 minutes). This indicates that the charger is in a “trickle – charge” mode. The
duration of time that the charger remains in this mode is dependent on the level of
remaining charge in the battery when it is first connected to the charger.
When the mains supply is connected to the charger, the green LED marked
“power” will light. Whe n a battery is placed into the charger and the charging cycle
is complete (normally 4-5 hours), the second green LED, marked “Charge
complete” will light.
7.2.3 Disposal of Batteries
Dispose of batteries in accordance with the applicable local regulations (these can
vary from country to country).
(In most countries, the trashing of used batteries is forbidden and the end-users
are invited to dispose them properly, eventually through not-for-profit profit
organisations, mandated by local governments or organised on a voluntary basis
by professionals).
Where the Tempus 2000 is marked with a CAA (UK Civil Aviation Authority) Safety
Acceptance Approval Number, all defective or exhausted batteries must be
returned to RDT for proper disposal. Please contact RDT at the address given in
section 1.1 to obtain instructions prior to shipping.
7.3 Replacing the Fuse
A fuse holder is located on the bottom panel of the Tempus 2000 system unit.
The fuse may have blown if the Tempus 2000 will not operate when a suitably
charged battery is installed and the battery life indicator indicates that the battery is
OK.
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Tempus 2000
7.3.1 Removing the Fuse
To remove the fuse,
•
Remove the battery
•
Close the lid of the Tempus 2000
•
Turn the Tempus 2000 on its side
•
Insert the edge of a small coin into the slot in the fuse holder and gently twist
anti-clockwise about 1/4 of a turn to release the fuse holder
•
Withdraw the fuse holder
•
Remove the fuse from the fuse holder.
If the fuse is good, it should be possible to see a fine wire running the entire length
of the glass cylinder. If the fuse is blown, it may be possible to see a break in the
fine wire or the inside of the glass cylinder may be discoloured. The following
figure illustrates fuses which are OK and fuses which are blown.
•
It is not always possible to see whether the fuse is blown. If in any doubt,
replace the fuse.
7.3.2 Fuse Replacement Type
WARNING
It is essential that the fuse is only replaced with one of the correct type and
rating described below. Use of a different type or rating of fuse may cause
damage to the Tempus 2000 or reduce the protection against risk of fire that
the fuse provides. Replacement fuses should only be obtained from Remote
Diagnostic Technologies Ltd. or their agents.
The correct fuse type is 20mm, low capacity (glass body), 4A, anti-surge (type T).
Replacement fuses are available from Remote Diagnostic Technologies Ltd.
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7.3.3 Replacing the Fuse
WARNING
Use of excessive force in the following steps may result in breakage of the
glass fuse and consequent risk of personal injury or area contamination
from broken glass.
This procedure applies equally to a new fuse or refitting the original fuse if it is not
blown.
To replace the fuse,
•
Gently insert the fuse into the end cap of the fuse holder.
•
Hold the end cap and slide the fuse into the fuse holder on the underside of the
Tempus 2000.
•
Insert the edge of a small coin into the slot in the fuse holder and gently twist
clockwise about 1/4 of a turn to secure the fuse holder. Only a small amount of
force is required.
7.4 Periodic Preventive Maintenance
The Tempus 2000 must be returned to the manufacturer every 10-14 months for
preventive maintenance. This includes, but is not necessarily limited to, factory
recalibration of sensors, cleaning, and the replacement of worn, damaged or
suspect parts.
Please contact the manufacturer at the address in section 1.1 to arrange
preventive maintenance. Please note that all returns must be performed within
the restrictions of RDT’s Terms and Conditions of Sale.
The Tempus 2000 should be securely repackaged in its original shipping materials
prior to dispatch for preventive maintenance. Do not include consumable materials
when packing for periodic maintenance. Contact the manufacturer if the original
shipping material is not available, or damaged, or if you have any other queries on
returns.
7.4.1 Cleaning by Manufacturer
If the Tempus 2000 becomes soiled with bodily fluids or tissues it must be returned
to the manufacturer for specialist cleaning and refurbishment. Please contact the
manufacturer for instructions.
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Tempus 2000
Spares List
8.1 Spares List
The following user-replaceable parts are available from the manufacturer at the
address in section 1.1.
Part number
Description
01-0001
Blood Pressure Cuff – Child (US)
01-0002
Blood Pressure Cuff – Adult (US)
01-0003
Blood Pressure Cuff – Large Adult (US)
01-0004
Alcohol Wipes (Box of 100)
01-0006
Nail Varnish Remover Swabs (Box of 100)
01-0007
ECG Spray
01-0009
Thermometer Cover Dispenser (Dispenser of 25)
01-0012
Fuse
01-0013
Battery Charger
01-0014
Battery Rechargeable
01-0016
Capnometer Cannula/Filter
01-0017
Blood Pressure Cuff – Child (EU)
01-0018
Blood Pressure Cuff – Adult (EU)
01-0019
Blood Pressure Cuff – Large Adult (EU)
41-0001
Tempus 2000 User Manual
41-0003
Battery Charger User Manual
01-0022
Tempus 2000 Repack Kit*
01-0024
Tempus 2000 Telecoms Extension Cable
01-0028
Earpiece Covers (Pack of 60)
*Note that the Tempus 2000 may be re-stocked by means of a kit that is available
from RDT. The kit contains: 4 off of the individual covers for the Earpiece, 2 off
packs of Cannula and Filters, 4 off of the individual Nail Varnish Remover Swabs,
4 off of the individual Alcohol Wipes, 1 off full ECG Spray Bottle and 1 off full box
of Thermometer Covers.
The kit is intended to be used to completely restock a single Tempus 2000 system.
All usable items within the Tempus 2000 should be discarded. The items
contained within the kit must only be used with the Tempus 2000.
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System Configuration
9.1 General
A number of the parameters used by the Tempus 2000 are configurable to suit
certain requirements. An example of this is the Response Centre telephone
numbers - should these change, the new numbers can be programmed in to the
Tempus 2000.
If you pressed the
button in the Advanced Help Menu, the Tempus 2000 will
display the System Configuration Menu. This is shown below.
From this point you can access the configuration screens for the ECG (where you
can change the filter frequency settings) or for the telecoms connections (where
the telephone numbers of the Response Centre are stored).
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Tempus 2000
You should only access these areas if you need to, and you should always ensure
that you have enough time to ensure that the changes yo u make are the correct
ones. If you make any changes, you will be asked by the Tempus 2000 to press
the
and the
buttons to confirm the changes you have made. The
Tempus 2000 will require you to repeat this key combination to ensure that you
definitely want to make the change. This procedure is designed to prevent the
settings from being changed inadvertently because, once the changes are made,
they become the default settings that the Tempus 2000 will always use.
Consequently, if you make changes to the connection configuration details that are
incorrect, you will not be able to subsequently achieve a connection until the
mistake is corrected. So you should always be sure that you are making a valid
change before you confirm the new setting.
9.2 ECG Configuration
If you press the
button in the System Configuration menu, you will be able to
switch between 50Hz and 60Hz filtering of the ECG. You will also be able to put
the ECG in demonstration Mode (for training purposes). In this mode the device
will display a computer generated ECG instead of a “real” trace when monitoring
and recording.
Follow the on screen instructions to edit the numbers as necessary.
9.3 Connection Configuration
If you press the
button in the System Configuration menu, you will be able to
edit the communications settings.
This screen is divided into two areas, upper and lower. In the upper section are
the Communications Configuration details, these can be reset by you. In the lower
area is the Device Information section. This contains the device serial number and
the software version number. You may occasionally need to refer to this
information when dealing with RDT, but generally it is not information that you
need to know.
Follow the on screen instructions to edit the numbers as necessary.
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10 Specifications and Standards
10.1 Specifications
Note that all figures quoted are based on room temperature, pressure and humidity unless
otherwise stated.
10.1.1 Thermometer
Measurement range
18ºC to 43ºC (target)
Type
Tympanic
Resolution
0.1ºC
Accuracy
±0.1ºC
10.1.2 Electrocardiograph
Input impedance
>100MΩ
Dynamic range
±5.28mV AC
Accuracy
±4%
DC offset
±300mV DC
Frequency response
0.05Hz to 100Hz
Sample rate
300Hz
Sample resolution
2.58µV (LSB), 12 bit resolution
Common mode rejection
96dB
50Hz/60Hz rejection
selectable, implemented through software filter
Defibrillator discharge protection Yes
Maximum defibrillator voltage
5kV (all units are individually tested)
Leakage current
<1µA
Pacemaker detection
No
Pulse rate ranges
No hardware limitation. Measurement software
reads to 250bpm. Higher rates will not be
measured, but are still represented correctly in
ECG graphs.
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Tempus 2000
10.1.3 Non-invasive Blood Pressure
10.1.3.1
10.1.3.2
Adult cuff and Large Adult cuff ratings
Systolic
60 - 250 mmHg
Diastolic
40 - 220 mmHg
Range
0 - 330 mmHg
Accuracy
± 3mmHg or ± 2% (whichever is greater)
Resolution
1 mmHg
Maximum inflation
330mmHg
Child cuff ratings
Systolic
60 - 250 mmHg
Diastolic
40 - 220 mmHg
Range
0 - 330 mmHg
Accuracy
± 3mmHg or ± 2% (whichever is greater)
Resolution
1 mmHg
Maximum inflation
330mmHg
10.1.4 ETC02 sensor
Range
0-100 BPM
Accuracy
± 2 BPM
Range
0-10% CO2 displayed value
Accuracy
± 5% (of full scale)
Rise time
<2 seconds
Delay time
5 seconds
Operating altitude range
0-15000 feet
10.1.5 Sp0 2 sensor
Range
30-240 bpm
Graphic display range
50-200 bpm
Accuracy
± 3bpm or ±2% whichever is greater
Resolution
1%
Range
50% to 100%
Graphic display range
50-100%
Accuracy
±2% at 70%-100%, ±3% at 50%-69%
Type
Functional saturation (test methods available
upon request)
Wavelength range
Red 660nm, infra-red 905nm
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10.1.6 Environmental Specifications
Altitude
0-4500m (0-15000ft)
(can be used at higher physical altitudes
provided the local atmosphere is no higher than
4500m, e.g. in a pressurised aircraft cabin)
Relative humidity
15%-95% (non-condensing)
Operating temperature range
0ºC to 40ºC
Storage temperature range
-20ºC to +60ºC
Environmental protection
IPX1, 30G shock
10.1.7 Miscellaneous Features and Specifications
10.1.7.1
10.1.7.2
Dimensions
L 300mm, W 270mm, D 240mm
Mass
7.2kg (without batteries)
Rechargeable battery
Battery life
4 hours running in normal use (battery life is
shortened by approximately 20 minutes if only
the built in Cell Phone is used)
Nominal voltage
14.4V
Charging voltage
16.4V ±1%
Nominal capacity
5.5Ah
Shelf life
2 years
Weight
0.8kg
Shelf life
2 years (before re-charging is required)
Overall rate of charge loss
10% maximum per year (dependant on
treatment)
Battery charger
Mains input voltage
100-250V (19Vdc input to charger)
Frequency
50-60Hz
Input power
45W max
Output voltage
16.4V dc
Output current
3A
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Tempus 2000
10.1.8 Communications
10.1.8.1
Types of Communications
Low Speed Communications
Transmits voice and data via two modems at
2.4 kbaud (ITU-T V.34, data compression
V22bis)
Medium Speed Communications Transmits simultaneous voice and data over a
single modem - OPTIONAL
Wireless Communications
10.1.8.2
Transmits simultaneous voice and data over a
single built in Cell Phone (tri-band GSM).OPTIONAL
Connection Compatibility
The Tempus 2000 is designed to operate with any telephone line which provides
an "RJ11" type connection with an analog interface. Typically, this includes aircraft
telephones and many fixed-line sockets. RJ11 connectors are widely used in the
USA.
Adapters are available to permit the Tempus 2000 to operate with other types of
telephone line socket.
10.1.8.3
Cell Phone (GSM) Specifications
Dimension
GSM 900 / E-GSM GSM 1800
900
GSM1900
Frequency range
TX: 880-914MHz
TX: 1710-1785MHz
TX: 1850-1910MHz
RX: 925-959MHz
RX: 1805-1880MHz
RX: 1930-1990MHz
Channel spacing
200kHz
200kHz
200kHz
Number of
channels
175 Carriers * 8
(TDMA)
374 Carriers * 8
(TDMA)
299 Carriers * 8
(TDMA)
Modulation
GMSK
GMSK
GMSK
TX Phase
accuracy
5° (RMS)
5° (RMS) 20° (peak)
5° (RMS) 20° (peak)
Duplex spacing
45MHz
95MHz
80MHz
Frequency stability
0.1ppm
0.1ppm
0.1ppm
Transmitter RF
power output
33dBm Class 4
2W peak
30dBm Class 1 1W
peak
30dBm Class 1 1W
peak
Transmitter
spurious emission
According to GSM
spec
According to GSM
spec
According to GSM
spec
Receiver RF level
-102dBm
-102dBm
-102dBm
Receiver RX bit
error rate
<=10-4 (Static Ch.)
<=10-4 (Static Ch.)
<=10-4 (Static Ch.)
<=3% (EQ50)
<=3% (EQ50)
<=3% (EQ50)
20° (peak)
Note that the US FCC Grantee code for the Cell Phone is ROS0002.
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10.1.9 Classification
The system is classified according to the requirements of EN60601-1:1990 inc.
A13:1996, the standard for Medical Electrical Equipment, Part 1, General
Requirements for Safety, Clause 5 as:
5.1
5.2
5.3
5.4
5.5
5.6
Internally (battery) powered
Applied parts type CF defibrillator proof (ECG electrodes), type BF
defibrillator proof (capnometer cannula, pulse oximeter probe, non-invasive
blood pressure cuff) and type BF (thermometer).
IPX1, protected against rainfall according to IEC529 (with the display
closed)
No parts supplied sterile or suitable for/requiring sterilising
Equipment not suitable for use in the presence of a flammable anaesthetic
mixture with air or with oxygen or nitrous oxide
Suitable for continuous use (8 hours maximum before the battery will
require replacement).
10.2 Standards Compliance
The Tempus 2000 complies with the applicable parts of the following standards:
•
IEC/EN60601-1:1990 inc. amendment A2:1995 and A13:1996, general
requirements for the safety of electrical medical products
•
IEC/EN60601-1-2:2001, collateral requirements for electromagnetic
compatibility, requirements and tests
•
IEC 60601-1-4, First edition, 1996 Collateral standard: programmable electrical
medical systems (software)
•
IEC 60601-2-27, First edition, 1994 Particular requirements for
electrocardiographic monitoring equipment
•
IEC 60601-2-30, First edition, 1995 Particular requirements for automatic
cycling indirect blood pressure monitoring equipment
•
ISO 9918, First edition, 1993 Particular requirements for capnometers for use
with humans
•
ISO 9919, First edition, 1992 Particular requirements for pulse oximeters for
medical use
•
RTCA/DO-160D Environmental conditions and test procedures for airborne
equipment
•
EN60529:1992 Degrees of protection provided by enclosures (approved to
IPX1)
•
BS2G 239:1992 Specification for Primary active lithium batteries for use in
aircraft
•
3GPP TS 51.010-1 Digital cellular telecommunications system (Phase 2+);
Mobile Station (MS) conformance specification; Part 1: Conformance
specification
•
EN301489-1 Electromagnetic compatibility and Radio Spectrum Matters
(ERM); Electromagnetic Compatibility (EMC) standard for radio equipment and
services; Part 1: Common technical requirements.
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•
Tempus 2000
EN301489-7 Part 7: Specific conditions for mobile and portable radio and
ancillary equipment of digital cellular radio telecommunications systems (GSM
and DCS).
10.2.1 Other Standards Being Used for Reference Purposes
The following standard is used for reference in the design of the Tempus 2000:
•
IEC/EN60945:1997 Maritime navigational equipment - General requirements Method of testing and required test results
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11
Symbols Used on the Tempus 2000
The following symbols are used on the Tempus 2000:
Symbol
Description
Defibrillation proof type CF applied part, The ECG
electrodes are floating from earth and meet the
patient leakage current requirements of EN606011:1990 Inc A13:1996 for type CF applied parts. The
ECG electrodes are proof against the effects of a
cardiac defibrillator discharge.
Defibrillation proof type BF applied part. The blood
pressure cuffs, the capnometer cannula and the pulse
oximeter probe are floating from earth and meet the
patient leakage current requirements of EN606011:1990 inc. A13:1996 for type BF applied parts. The
applied parts listed are proof against the effects of a
cardiac defibrillator discharge.
Type BF applied part. The thermometer is floating
from earth and meet the patient leakage current
requirements of EN60601-1:1990 inc. A13:1996 for
type BF applied parts. The thermometer is not proof
against the effects of a cardiac defibrillator discharge.
Hazardous voltage. Do not tamper with the internal
components or connections of this device. Always
follow instructions when replacing the battery.
Attention, consult accompanying documents
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Tempus 2000
Symbol
Description
Battery area
Battery power level
System power on/off (push/push)
Date of manufacture, where the year that the item
was manufactured is represented by the year and
then the month e.g. 2002 06 is June 2002.
YYYY - MM
Single use device only, discard item after use
IPX1
The device is proof against light rain according to
IEC529
The device has been declared by the manufacturer to
be in accordance with the requirements of the
European Union Medical Devices Directive
93/42/EEC as transposed by UK national legislation.
YYYY - MM
CUD-34 Revision 00
Shelf life, where the time that the unit must be used
by is represented by the year and then the month e.g.
2004 06 is June 2004.
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Symbol
LOT YYYY - MM
Description
Where the year that the item was manufactured as a
part of a larger batch is represented b y the year and
then the month e.g. 2002 06 is June 2002.
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12
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Tempus 2000
Terms and Conditions of Sale
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User/Operator Manual
13 Software License Agreements
This product incorporates software object code licensed by Remote Diagnostic Technologies Ltd. The software is licensed,
not sold. All rights reserved. If you do not agree to this End User License Agreement ("EULA"), do not use the device or
copy the software. Instead, promptly contact Remote Diagnostic Technologies Ltd for instructions on return of the unused
device(s) for a refund. Any use of the software, including but not limited to use on the device, will constitute your agreement
to this EULA. The agreement: (i) prohibits any disassembly, decompilation, and/or reverse engineering or any other action
attempting to discover or disclose the source code or methods or concepts embodied in the source code; (ii) the software
and chipset copyright, trademark other proprietary notices and confidential legends shall not be altered; (iii) all warranties
associated with the software object code shall be no greater than the license agreement made between Remote Diagnostic
Technologies Ltd and its licensor, (iv) the liability of the licensor shall be limited and shall be no greater than that expressly
set forth in the license agreement between Remote Diagnostic Technologies Ltd and the licensor.
END USER LICENSE AGREEMENT
You have acquired a device TEMPUS 2000 that includes software licensed by REMOTE DIAGNOSTIC TECHNOLOGIES
LTD. from Microsoft Licensing Inc. (MS) or its affiliates EURODIS BYTECH LIMITED. Those installed software products of
MS origin, as well as associated media, printed materials, and “online” or electronic documentation (“SOFTWARE”) are
protected by international intellectual property laws and treaties. The SOFTWARE is licensed, not sold. All rights
reserved.
IF YOU DO NOT AGREE TO THIS END USER LICENSE AGREEMENT (“EULA”), DO NOT USE THE DEVICE OR COPY
THE SOFTWARE. INSTEAD, PROMPTLY CONTACT REMOTE DIAGNOSTIC TECHNOLOGIES LTD. FOR
INSTRUCTIONS ON RETURN OF THE UNUSED DEVICE (S) FOR A REFUND. ANY USE OF THE SOFTWARE,
INCLUDING BUT NOT LIMITED TO USE ON THE DEVICE, WILL CONSTITUTE YOUR AGREEMENT TO THIS EULA
(OR RATIFICATION OF ANY PREVIOUS CONSENT).
GRANT OF SOFTWARE LICENSE. This EULA grants you the following license:
You may use the SOFTWARE only on the DEVICE.
NOT FAULT TOLERANT. THE SOFTWARE IS NOT FAULT TOLERANT. REMOTE DIAGNOSTIC TECHNOLOGIES
LTD. HAS INDEPENDENTLY DETERMINED HOW TO USE THE SOFTWARE IN THE DEVICE, AND MS HAS RELIED
UPON REMOTE DIAGNOSTIC TECHNOLOGIES LTD. TO CONDUCT SUFFICIENT TESTING TO DETERMINE THAT
THE SOFTWARE IS SUITABLE FOR SUCH USE.
NO WARRANTIES FOR THE SOFTWARE. THE SOFTWARE is provided “AS IS” and with all faults. THE ENTIRE
RISK AS TO SATISFACTORY QUALITY, PERFORMANCE, ACCURACY, AND EFFORT (INCLUDING LACK OF
NEGLIGENCE) IS WITH YOU. ALSO, THERE IS NO WARRANTY AGAINST INTERFERENCE WITH YOUR
ENJOYMENT OF THE SOFTWARE OR AGAINST INFRINGEMENT. IF YOU HAVE RECEIVED ANY WARRANTIES
REGARDING THE DEVICE OR THE SOFTWARE, THOSE WARRANTIES DO NOT ORIGINATE FROM, AND OR NOT
BINDING ON, MS.
Note on Java Support. The SOFTWARE may contain support for programs written in Java. Java technology is not fault
tolerant and is not designed, manufactured, or intended for use or resale as online control equipment in hazardous
environments requiring fail-safe performance, such as in the operation of nuclear facilities, aircraft navigation or
communications systems, air traffic control, direct life support machines, or weapons systems , in which the failure of Java
technology could lead directly to death, personal injury, or severe physical or environmental damage. Sun Microsystems,
Inc. has contractually obligated MS to make this disclaimer.
No liability for Certain Damages. EXCEPT AS PROHIBITED BY LAW, MS SHALL HAVE NO LIABILITY FOR ANY
INDIRECT, SPECIAL, CONSEQUENTIAL OR INCIDENTIAL DAMAGES ARISING FROM OR IN CONNECTION WITH
THE USE OR PERFORMANCE OF THE SOFTWARE. THIS LIMITATION SHALL APPLY EVEN IF ANY REMEDY FAILS
OF ITS ESSENTIAL PURPOSE. IN NO EVENT SHALL MS BE LIABLE FOR ANY AMOUNT IN EXCESS OF U.S. TWO
HUNDRED FIFTY DOLLARS (U.S.$250.00).
Limitations on Reverse Engineering, Decompilation, and Disassembly. You may not reverse Engineer, decompile, or
disassemble the SOFTWARE, except and only to the extent that such activity is expressly permitted by applicable law
notwithstanding this limitation.
SOFTWARE TRANSFER ALLOWED BUT WITH RESTRICTIONS. You may permanently transfer rights under this EULA
only as part of a permanent sale or transfer of the Device, and only if the recipient agrees to this EULA. If the SOFTWARE
is an upgrade, any transfer must also include all prior versions of the SOFTWARE.
EXPORT RESTRICTIONS. You acknowledge that SOFTWARE is of US-origin. You agree to comply with all applicable
international and national laws that apply to the SOFTWARE, including the U.S. Export Administration Regulations, as well
as end-user, end-use and country destination restrictions issued by U.S. and other governments. For additional information
on exporting the SOFTWARE, see http://www.microsoft.com/exporting/
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14
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Tempus 2000
FCC Supplier’s Declaration of Conformity
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Title                           : CUD-34 Revision 00 Tempus 2000 User Manual.doc
Creator                         : channan

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