Medtronic CARELINK 2090 Reference Manual

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2001
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2002
MEDTRONIC CARELINK™ 2090
Programmer for Medtronic and Vitatron Devices
Programmer Reference Guide
2090/9986/SW007:
VSC01:VSC01:
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Contents

1 Introduction to the Programmer 7

Explanation of packaging and product symbols 8
About this guide 10
Description and intended use 10
Warnings 11
Precautions 12
Declaration of Conformity 15
Regulatory compliance 15
Security features for the Windows XP operating system 16
Software requirements 17
Programmer functions 18
System components 20
Display screen features 27

2 Set up the Programmer 31

Basic setup 32
Connect peripheral devices 37

3 Conduct a patient session 39

Prepare for a patient session 40
Initiate a patient session 51
End a patient session 55
Store components 56

4 Manage reports and data 57

Reports 58
Session data 58
Save to a PDF file 58
Save to diskette 59
Save to USB 59
View reports that are saved to media 61
Vitatron Manual-Guided Reset 62

5 Use printers 63

Use external printers 64
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Contents
Install printer paper 67
Printer buttons 68
Tear off a printout 69
Low paper supply 69

6 Select options 71

About the between sessions tool palette 72
Adjust Programmer time and date 73
Select audible tones 74
Set the interval for report deletion 75
Manage patient data privacy 76
Change the language setting 79
Improve the detection of pacing artifacts 79
Check the software version 80
Start the demonstrations option 81
View and update Programmer location and hardware information 81
Select other software 83
Remove other software applications 83
Obtain technical manuals 84

7 Service the Programmer 85

Programmer Reference Guide
Clean the system components 86
Sterilize the programming head, ECG cable, and lead wires 86
Replace a PC card 87
Programmer specifications 88
Special notice 91
Medtronic limited warranty 92

Index 93

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Medtronic CareLink 2090 0
Programmer Reference Guide 0
A guide for setting up and using Medtronic CareLink 2090 Programmer.
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The following are trademarks or registered trademarks of Medtronic in the United States and possibly in other countries: CareLink, Jewel, Marker Channel, Medtronic, Medtronic CareLink, Paceart, Reveal and Vitatron
All other trademarks are the property of their respective owners.
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Introduction to the Programmer1

Explanation of packaging and product symbols 8
About this guide 10
Description and intended use 10
Warnings 11
Precautions 12
Declaration of Conformity 15
Regulatory compliance 15
Security features for the Windows XP operating system 16
Software requirements 17
Programmer functions 18
System components 20
Display screen features 27
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Chapter 1

Explanation of packaging and product symbols

Explanation of packaging and product symbols
Refer to the package label and product to see which symbols apply to this product.
Conformité Européenne (European Conformity). This symbol means that the device fully complies with European Directive AIMD 90/385/EEC (NB 0123). (Applies to Medtronic hardware and software only.)
Conformité Européenne (European Conformity). This symbol means that the device fully complies with European Directive AIMD 90/385/EEC (NB 0344). (Applies to Vitatron desktop software only.)
Conformité Européenne (European Conformity). This symbol means that the device fully complies with the essential requirements of R&TTE Directive 1999/5/EC (NB 1856). (Applies to R&TTE only.)
Caution
Consult instructions for use
Programmer Reference Guide
The product complies with both Canadian and U.S. requirements for meeting UL safety standards.
Type BF applied part
Type CF applied part
Serial number
Temperature limitation
For U.S. audiences only.
Off
On
Wireless communication enabled
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Introduction to the Programmer
EC REP
Explanation of packaging and product symbols
Do not dispose of this product in the unsorted municipal waste stream. Dispose of this product according to local regulations. See http://recycling.medtronic.com for instructions on proper disposal of this product.
RF transmitter
Caution: Strong magnet
This symbol means that the device fully complies with the Australian Communications and Media Authority (ACMA) and the New Zealand Ministry of Economic Development Radio Spectrum Management standards for radio communications products.
Battery
Diskette
Network connection port
USB port
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Printer port
Microphone port
Headphones port
Authorized representative in the European community
Alternating current
Date of manufacture
Manufacturer
Reorder number
Lot number
Programmer Reference Guide
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Chapter 1

About this guide

About this guide
This guide describes the features and functions of the Medtronic CareLink 2090 Programmer (referred to as the “Programmer”).

Description and intended use

Humidity limitation
Package contents
Programmer, software installed
Product documentation
Accessories
The Medtronic CareLink 2090 Programmer is a portable, line-powered (AC) microprocessor based system with software to interrogate and program Medtronic and Vitatron implantable devices. Other features include:
Programmer Reference Guide
Automated software updates using a dial-up or local area network (LAN) connection, depending on the hardware configuration. This allows the Programmer to program new devices and to provide new features as they become available.
A large, bright screen that is adjustable for viewing when sitting or standing.
Keyboard to make entering information easier.
Fast printing speed of 50 mm per second on recorder paper.
ECG recording and diagnostic data reporting. Refer to the technical manuals supplied with the software and hardware accessories for specific details.
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Warnings

Introduction to the Programmer
Warnings
These warnings apply in general to using the Programmer for programming implantable device parameter settings. Refer to the reference guides for the implantable device and the Programmer software for more information related to specific implantable device models.
Modification of equipment – Do not modify this equipment. Modifications may reduce system effectiveness and impact patient health.
Telecom voltage limitation – When using a modem or combo card, make sure that the telecom voltage does not exceed 125 V. Excessive voltage may damage the programmer.
Importance of reference documentation – Implantable device programming should be done only after careful study of the reference guide for the implantable device and after careful determination of appropriate parameter values based on the patient’s condition and pacing system used. The implantable device reference guide contains a complete description of implantable device operation and important information, such as indications for use, contraindications, warnings, and precautions. The instructions contained in this reference guide and the reference guide supplied with the Programmer software are limited to the mechanics of setting up the Programmer and selecting the correct options for the desired programming function. Improper use of the Programmer could result in erroneous or inadvertent programming and improper operation of telemetry and measurement functions.
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Measurement function – The Programmer is also intended to detect and measure pulse rate, AV interval and pulse width, and implantable device artifacts. The device takes these digital measurements with the assistance of optional skin electrodes. Medtronic and Vitatron make no claims or warranties as to the effectiveness of the Programmer as a diagnostic tool to the physician.
Programmer Reference Guide
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Chapter 1

Precautions

Precautions
Equipment compatibility – The Programmer must be used only
for interrogating and programming compatible Medtronic or Vitatron implantable devices. Direct stimulation through energy coupling may occur if the Programmer is used on other implanted devices. The Programmer is not compatible with programmable devices of other manufacturers.
Internal electrodes – Do not connect the Programmer to wires or electrodes internal to the body. The Programmer is designed to be medically safe only when attached to surface electrodes.
Defective equipment – If technical and safety inspection reveals a defect which could harm the patient, clinicians, or third parties, the device should not be used until it has been properly repaired. The operator must immediately notify Medtronic or Vitatron of these defects.
VGA monitor use – To protect against interference or surge/leak currents, the use of a secondary VGA monitor that meets an applicable safety standard such as UL 60950 or IEC 60950 is strongly recommended.
ECG cable integrity – Upon opening the package, if the ECG cable appears damaged, do not use it. Contact your local Medtronic or Vitatron representative.
Care in handling ECG cable wire – Do not pull on the insulated cable wire to disconnect the cable. Tension on the insulated cable wire may result in damage to the cable.
Electrocautery / external defibrillation – Do not position the programming head over an implanted device during electrocautery or external defibrillation procedures.
Do not immerse – Take care to prevent liquid from entering the Programmer and programming head. Do not immerse the Programmer or any accessories in any liquid or clean them with aromatic or chlorinated hydrocarbons.
Programmer Reference Guide
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Introduction to the Programmer
Precautions
Autoclaving – Do not autoclave the programming head or ECG cable and lead wires.
Electromagnetic interference (EMI) – The programming head has been tested for compliance with industrial EMI regulations. Any use outside the patient environment may result in the programming head malfunctioning.
Radio-frequency (RF) interference – Portable and mobile RF communications equipment can interfere with the Programmer’s operation. Although this transmitter has been approved by the Federal Communications Commission, there is no guarantee that it will not receive interference or that any particular transmission from this transmitter will be free from interference.
Damaged equipment – If the case of the Programmer is cracked or if any of the connectors are damaged, contact your Medtronic or Vitatron representative. If there is insulation damage to the power cord or accessory cables or if any of the wall or equipment plugs are damaged, please replace the part and dispose of it according to local regulations or return the part to Medtronic.
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Electrode quality – Use of high-quality silver/silver chloride (Ag/AgCl) electrodes can minimize the occurrence of small DC voltages that can block the ECG signal. Use electrodes that are fresh and from the same box. Prepare the patient’s skin according to the directions provided with the electrodes.
Flammable anaesthetic mixture – The Programmer is not suited for use in the presence of a flammable anaesthetic mixture.
Avoid damage from programming head – Keep the programming head away from any device or material that will be damaged by the magnetic field, including computer diskettes.
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Chapter 1
Precautions
Environmental precautions
To ensure safe and effective operation, use the device with care to avoid damage to the Programmer from environmental factors that may impair its function. Care is exercised in design and manufacturing to minimize damage to devices under normal use. However, electronic devices are susceptible to many environmental stresses including, but not limited to, the following examples.
The unit should not be dropped or mishandled in such a manner as to cause physical damage to the unit. This may impair device function. Even if the unit works immediately after being dropped, operational damage may have occurred that may not be observed until some future time.
Fluid should not be spilled on the unit. Even though care is exercised in design and manufacture of the unit to minimize leakage, fluid incursion may occur, which could impair functioning of the unit.
The Programmer may be affected by electrostatic discharge (ESD). In an environment likely to cause ESD, such as a carpeted floor, you should discharge any charge collected on your body before touching the device.
Electrically-operated medical devices, such as the Programmer require special care (in terms of EMC) when being installed. Refer to the accompanying insert: Electromagnetic Compatibility Declaration.
Do not open the device. The Programmer is constructed to minimize risk from environmental factors. Opening the unit may make the unit susceptible to environmental factors.
Rapid temperature changes may affect proper operation. Always allow the temperature to stabilize in the environment in which the device is used before using the device.
Prolonged storage or operation of the device in high humidity may affect proper operation.
If there is any concern that damage has occurred, the unit should be returned to Medtronic or Vitatron for inspection and any needed repair.
Besides these listed examples, various other environmental factors may impair proper performance of the unit in the hospital setting. Always use good health management practices to prevent environmental damage to the unit.
Programmer Reference Guide
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Declaration of Conformity

Medtronic declares that this product is in conformity with the essential requirements of Directive 1999/5/EC on Radio and Telecommunications Terminal Equipment and Directive 90/385/EEC on Active Implantable Medical Devices (AIMD).
For additional information, contact Medtronic or Vitatron at the telephone numbers and addresses provided on the back cover of this manual.

Regulatory compliance

Industry Canada
ID:3408D-MICS
Operation is subject to the following two conditions: (1) this device may not cause interference, and (2) this device must accept any interference, including interference that may cause undesired operation of the device.
Introduction to the Programmer
Declaration of Conformity
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This device may not interfere with stations operating in the
400.150-406.000 MHz band in the meteorological aids, meteorological-satellite, and earth exploration-satellite services and must accept any interference received, including interference that may cause undesired operation.
Australia / New Zealand
The device fully complies with Australian Communications and Media Authority (ACMA) and the New Zealand Ministry of Economic Development Radio Spectrum Management standards. The C-tick symbol indicates that the product complies with the applicable EMC/Radio standard for radio communications products.
US Federal Communications Commission (FCC)
FCC ID:LF5MICS (for Programmer) FCC ID:LF59767 (for Programming head)
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Chapter 1

Security features for the Windows XP operating system

The following provision applies to the low frequency communications system in the device:
This device complies with Part 15 of the FCC Rules respectively. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation. The user is cautioned that changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment.
The following provision applies to the UHF communications system in the device:
This transmitter is authorized by rule under the Medical Device Radio Communications Service (47 C.F.R. Part 95) and must not cause harmful interference to stations operating in the 400.150 -
406.000 MHz band in the Meteorological Aids (i.e., transmitters and receivers used to communicate weather data), the Meteorological Satellite, or the Earth Exploration Satellite Services and must accept interference that may be caused by such aids, including interference that may cause undesired operation.This transmitter shall be used only in accordance with the FCC Rules governing the Medical Device Radio Communications Service. Analog and digital voice communications are prohibited. Although this transmitter has been approved by the Federal Communications Commission, there is no guarantee that it will not receive interference or that any particular transmission from this transmitter will be free from interference.
Security features for the Windows XP operating system
The operating system software for the Programmer is Microsoft Windows XP.
The popularity of Windows XP has made it a common target for threats including network attacks and viruses. In addition, many of the features on the Programmer rely on connecting to a hospital or clinic network. The great benefit of features that rely on network connections comes with a slight increase in the possible vulnerability of the Programmer to network-originated threats.
Programmer Reference Guide
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Introduction to the Programmer

Software requirements

What Medtronic has done to promote security on the Programmer
Medtronic has gone to great lengths to promote the safety and reliability of the Programmer. The Programmer is configured as a special purpose device, with no general purpose access. Because unnecessary software components such as Internet Explorer and Microsoft Office are common targets of malicious attacks, those components are not installed on the Programmer.
The operating system portion of the internal hard disk is write-protected. Each time the Programmer is restarted, it starts in a known good state. Unsupported hardware, including unsupported PCMCIA cards or USB devices, are ignored by the operating system and cannot be accessed from the Programmer. Medtronic continues to work with its partners to analyze emerging threats and evaluate potential impact on the Programmer.
What hospitals and clinics can do to promote the security of Programmers
The most important step hospitals and clinics can take to minimize the chance of the Programmer’s security being compromised is to have a secure network. This includes firewalls and security policies to keep the network, and any devices connected to it, safe and free from security threats originating from outside the network. Some threats, such as denial-of-service attacks, which cause a targeted system to continually respond to bogus network requests, can only originate and affect systems at the local level.
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What to do if you suspect the Programmer has been compromised
If you believe the Programmer has been compromised by a security threat, turn off the Programmer, and disconnect it from the network or remove the network card, then restart the system. Contact your Medtronic or Vitatron representative for further assistance.
Software requirements
The Programmer requires software from Medtronic and Vitatron to operate. Once installed, the software remains on the Programmer hard drive.
Medtronic and Vitatron periodically update the software to add functions to the Programmer.
Programmer Reference Guide
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Chapter 1

Programmer functions

Programmer functions
Programming functions:
Telemetry functions:
The following list summarizes some of the Programmer functions. Specific functions depend on the implantable device model being programmed or monitored and the software installed.
Permanent and temporary adjustment of parameter values.
Selection of nominal parameter values established by Medtronic, Vitatron or by the user.
Emergency buttons for VVI pacing.
Automatic detection of the device model, and automatic application start-up, if the programming head is in proper position when the Programmer is turned on.
Automatic confirmation of a programmed change.
Reporting of currently programmed parameter values in effect and battery status of the implanted device.
Reporting of real-time measurements of implantable device operating parameters such as battery voltage, output energy, etc.
Display and printout of Marker Channel telemetry to simplify EGM analysis.
Display and printout of an atrial and/or ventricular intracardiac electrogram (EGM) taken from the electrodes of the implantable device lead system.
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ECG and other diagnostic functions:
ECG window on programming and telemetry data screens provides a continuous view of the patient’s ECG.
Full-window ECG display including a freeze option and an amplitude adjustment feature; ECG display includes Marker Channel telemetry, EGM waveforms, or both when available.
Continuous multi-channel recording (ECG and Marker Channel telemetry or ECG and EGM, for example).
Stimulation threshold test functions.
Direct measurement of pulse rate, AV interval, and pulse width.
Temporary implantable device inhibition.
Printout of programmed and measured information for permanent record.
Software update function:
Updates available from Medtronic personnel.
Clinical software applications that have Uninstall Software capability may be removed using the Programmer Desktop.
Introduction to the Programmer
Programmer functions
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Programmer Reference Guide
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Chapter 1

System components

System components
Figure 1-1. Programmer components - front view
1 Display screen
2 Emergency VVI
button
3 Microphone jack
4 Headphone jack
5 Keyboard cover
6 Keyboard
7 Printer controls
8 Telephone cord
(not supplied)
9 Printer paper
Note: Only accessories approved by the manufacturer should be used.
10 Programming
head (ordered separately)
11 Touch pen
12 Electrode leads
13 ECG cable
with plug
14 Reference guide
15 Disk drive, PC
card cover
16 Power cord
17 Ethernet cable
(not supplied)
Display screen – Display can be positioned smoothly from closed to nearly horizontal. Programming options are selected on the screen with the touch pen.
Programmer Reference Guide
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Introduction to the Programmer
System components
Emergency VVI button – Used to deliver bradycardia VVI operation.
Microphone jack – Intended for future use.
Headphone jack – Intended for future use.
Keyboard cover – Slides forward to protect the keyboard.
Keyboard – Used to enter information.
Printer controls – Select paper speeds of 12.5, 25, or 50 mm/s.
Push a button once to select printing speed. Push it again to stop printing. The Paper Advance button allows the user to properly align the paper.
Telephone cord – Connects the Programmer modem to a telephone jack. The telephone cord must be 26 wire gauge minimum. (Not supplied by Medtronic.)
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Ethernet cable – Used to connect the Programmer to the clinic’s network. The Ethernet cable must be Category 5 or better. (Not supplied by Medtronic.)
Printer paper – Paper for the internal printer.
Programming head – Provides the communication link between
the Programmer and the patient’s implantable device. The programming head contains a strong permanent magnet, radio-frequency (RF) transmitter and receiver, and light array. It must be held over the implantable device during a program or interrogate operation. (Ordered separately; not supplied with Programmer.)
Touch pen – Used to select options on the display screen. Predetermined options are selected by applying the pen to the screen.
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System components
Electrode leads / ECG cable – Connects the Programmer to skin electrodes on the patient for ECG and measurement functions requiring surface detection of cardiac and implantable device signals. Five color-coded lead wires connect the cable to standard, disposable skin electrodes applied to the patient.
Note: If you received a five-lead cable with a plug, the plug can be removed for five-lead ECG applications.
Reference guide – Programmer Reference Guide, provides information about setting up the Programmer and between session features.
Disk drive, PC card cover – Provides access to the disk drive and the PC card. If applicable to your Programmer hardware, also provides access to USB port(s) and either Integrated Ethernet or parallel connector.
Power cord – Connects the Programmer to an AC power outlet.
Figure 1-2. Front connectors (keyboard turned up)
1 Programming head (yellow marker)
2 Analog Input/Output (green marker)
3 ECG cable (black or blue marker)
Programming head – The programming head connector has a yellow marker.
Analog Input/Output – Allows an external monitor or recorder to be connected to the Programmer. This connector has a green marker.
Programmer Reference Guide
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Introduction to the Programmer
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4
System components
ECG cable – Connects the ECG cable to the Programmer. This connector has a black or blue marker.
Figure 1-3. Left view
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1ON/OFF switch
2 Cooling fan
3 Expansion slot
4Printer
ON/OFF switch – Controls power (AC) to the Programmer. Once the Programmer is turned off, wait 2 seconds before turning it on again.
Cooling fan – Internal fan provides continuous airflow to prevent the internal circuitry from overheating.
Expansion slot – Allows for additional features to be added, such as the Analyzer that is available as an option.
Printer – Integral thermal printer with text and graphic output capabilities. According to the selected function, the printer provides data reports or it can print out a continuous ECG with accompanying Marker Channel telemetry, EGM, or both when available.
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System components
Figure 1-4. Right view
1 Disk drive, PC card cover
2 Infrared window
Disk drive, PC card cover – Provides access to the disk drive and the PC card. If applicable to your Programmer hardware, also provides access to USB port(s) and either Integrated Ethernet or parallel connector.
Infrared window – Intended for future use.
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Introduction to the Programmer
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System components
Figure 1-5. Disk drive, PC card cover open (two variations of Programmer hardware are shown)
1PC card slot
2 Parallel connector
3 Disk drive
1PC card slot
2 Disk drive
3 Integrated Ethernet
4 USB port
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PC card slot – There are different types of PC cards that can be plugged into the PC card slot:
The Modem card.
The Combination Ethernet/Modem Network card, referred to as the combo card.
These PC cards can be used to connect to the Software Distribution Network.
Warning: When using a modem or combo card, make sure that the telecom voltage does not exceed 125 V. Excessive voltage may damage the Programmer.
Parallel connector – Allows a printer to be connected to the Programmer.
Disk drive – Accommodates a 90 mm formatted diskette that is IBM-compatible.
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System components
Integrated Ethernet – Allows the Programmer to connect to the Software Distribution Network and the Paceart data management system using an Ethernet connection.
Figure 1-6. Back view (power cord door open)
1 USB port(s)
2 VGA output port
3Power cord
USB port(s) – Allows installation of software, software updates, and future device application installations. The USB port can also be used to connect to a USB printer or a USB flash drive.
VGA output port – Allows porting the screen image of the Programmer to an external VGA monitor or for conversion of the output signal to NTSC/PAL format for presentation on a television monitor.
Caution: To protect against interference or surge/leak currents, the use of a secondary VGA monitor that meets an applicable safety standard such as UL 60950 or IEC 60950 is strongly recommended.
Power cord – Connects the Programmer to line (AC) power.
Programmer Reference Guide
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Introduction to the Programmer
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Display screen features

The Programmer display screen is an interactive device that displays text and graphics. It is also a control panel that displays buttons and menu options that you can select using the touch pen.
Features and conventions of the display screen
This section provides an overview of the features of the display screen. For more information, refer to the reference guide for the implanted device. Figure 1-7 shows the main elements of the typical screen. Vitatron display screens may be different; see the reference guide for the implanted device. If you see a button, select it to display the Vitatron Select Model screen.
Note: For information on changing the language (for example, from English to German), see “Change the language setting” on page 79.
Figure 1-7. Main elements of a display screen example
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Display screen features
1 Task bar
2 Status bar
3 Live Rhythm Monitor window
4 Waveform adjustment bars
5 Task area
6 Command bar
7 Buttons
8 Tool palette
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Display screen features
Task b a r
The task bar can contain these icons/indicators:
Tab le 1- 1. Task bar icons/indicators
Icon Name Function
Position head light array
Turns green to indicate successful communication between the programming head and the device. The greater the number of green bars on the array, the better the communication. A minimum of two green bars should be lit.
Analyzer indicator/selector
Device indicator/selector
USB indicator Turns green to indicate USB flash drive is
Diskette indicator Turns green to indicate diskette drive is
Used to start an analyzer session or, if your device supports concurrency, to switch to an analyzer session from a device session. When an analyzer session is running, the indicator box turns green. (For more information on the optional Analyzer, see the 2290 Analyzer Reference Guide.)
Used to go to the Select Model screen on the Programmer desktop or, if your device supports concurrency, to switch to a device session from an analyzer session. When a device session is running, the indicator box turns green.
available for saving PDF reports and patient data. When USB indicator is green, diskette is not available. When inserting a USB flash drive, you may experience a slight delay before device is available for use.
available for saving PDF reports and patient data. When diskette indicator is green, USB flash drive is not available.
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Introduction to the Programmer
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Display screen features
Status bar
Before selecting a model, the status bar has no information. For specific information about the status bar, refer to the reference guide for the implanted device. After model selection, the status bar may include:
The present pacing mode.
Test condition status.
The device model.
1 Status bar
Live Rhythm Monitor window
This window is a partial view of the full-screen display of the ECG, and contains a Status bar and a Waveform adjustment bar that lets you make changes to the waveform display. You can expand this window to its full size by selecting the small square button in the upper-right corner of the window or by selecting
[Adjust...].
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After model selection, Marker Channel and telemetered EGM waveform traces may be available.
Refer to the appropriate reference guide for the implanted device for more information about the Live Rhythm Monitor. Refer to the
2290 Analyzer
Reference Guide for information about the controls
on the Waveform Adjustment bar.
1 Waveform Adjustment bar
Task area
The portion of screen between the Live Rhythm Monitor window at the top and the command bar at the bottom changes according to the task or function you select.
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Display screen features
Command bar
The bar at the bottom of the screen shows the command buttons for automatically launching the proper software application and displaying the Vitatron Select Model screen. For information on what command buttons are available after selecting a model, see the reference guide for the implanted device.
Buttons
Buttons like those shown below let you operate the Programmer using the touch pen. You can “press” a button by touching it with the tip of the touch pen.
1 Inactive button (indicated by a lighter color)
Buttons may directly execute a command, such as they may open a window that prompts another action. Usually such buttons have a label ending with an ellipsis, such as
[Strips...] or [Adjust...].
A procedure may instruct you to “press and hold” a button. Press the tip of the touch pen to the button and maintain pressure until it is time to “release” the button.
When a button is inactive, it appears a lighter color and does not execute a command when you press it with the touch pen.
Tool palette
The collection of buttons and icons along the edge of the screen is referred to as the “tool palette.” These are the controls you will use to choose the task or function screen you want displayed. For more information, see “About the between sessions tool palette” on page 72. For information about the session tool palette, refer to the reference guide for the implanted device.
Programmer Reference Guide
[Freeze], or
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Set up the Programmer2

Basic setup 32
Connect peripheral devices 37
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Chapter 2

Basic setup

Basic setup
Position the display
Before setting up the Programmer, select a sturdy location for it without blocking the air vents on the right and left sides. The Programmer uses a power cord, so the location must be near an AC outlet.
This section describes how to:
Position the display
Connect the ECG cable
Connect the programming head
Connect the power cord
Connect the telephone line
Connect the Ethernet cable
Turn on the Programmer
Troubleshoot potential interference
Programmer Reference Guide
1. Press inward on the two buttons on each end of the handle.
2. Lift up the display
3. Place it at a comfortable viewing angle.
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Connect the ECG cable
About the ECG cable
The Medtronic Model 2090 EC/ECL ECG cable and lead wires connect the Programmer to skin electrodes for ECG and measurement functions requiring surface detection of cardiac and implantable device signals.
Set up the Programmer
Basic setup
1. Slide the keyboard cover all the way back. Press the latch and flip up the keyboard.
2. Line up the arrow on the ECG cable with the red dot on the ECG connector.
3. Plug the cable into the connector with the black or blue marker on the right.
4. Flip down the keyboard, making sure the cable passes through the notch on the right or left side.
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The ECG cable is designed for use with five lead wires. However, some physicians prefer to use only four lead wires. If four lead wires are used, insert the chest ECG plug into the middle cable port of the ECG cable.
Note: Improper insertion of the cable plug may damage the connector pins.
Cautions:
Upon opening the package, if the ECG cable appears damaged, do not use it. Contact your local Medtronic or Vitatron representative.
Do not pull on the insulated cable wire to disconnect the cable. Tension on the insulated cable wire may result in damage to the cable.
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Chapter 2
Basic setup
Connect the programming head
Connect the power cord
1. Slide the keyboard cover all the way back. Press the latch and flip up the keyboard.
2. Line up the red dots on the programming head cable and the programming head connector.
3. Plug the cable into the programming head connector with the yellow marker on the left.
4. Flip down the keyboard, making sure the cable passes through the notch on the right or left side.
1. Open the back cover by pressing on both latches.
2. Plug the power cord into the Programmer.
3. Plug the power cord into AC power outlet. The Programmer automatically adjusts to the available line power.
4. Make sure the power cord passes through the notch on the left side and close the cover.
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Set up the Programmer
2
3
2
Connect the telephone line
1. Locate the disk drive/PC card cover on the right side of the Programmer and flip down the cover.
2. Connect the telephone line to the RJ-11 connector on the modem card or combo card. (The combo card is shown.)
3. Connect the opposite end of the telephone line to an analog telephone jack.
4. If you replaced the card, you will need to reboot the Programmer before using it.
Connect the Ethernet cable (as applicable to your hardware)
1. Locate the disk drive/PC card cover on the right side of the Programmer and flip down the cover.
2. Connect the Ethernet cable to the Integrated Ethernet connection.
3. Alternatively, the Ethernet cable can be connected to the RJ-45 connector on the combo card instead of using the integrated Ethernet connection.
4. Connect the opposite end of the Ethernet cable to a network jack.
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Basic setup
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Chapter 2
Basic setup
Turn on the Programmer
1. Locate the ON/OFF switch on the left side of the Programmer.
2. Press inward on the top of the ON/OFF switch.
Notes:
The Programmer will not operate without the appropriate software installed. If the Programmer does not operate, check the version of software that is loaded on the Programmer, and update it if necessary.
The first time the Programmer is turned on following one of these changes, the start-up will take 2 minutes:
When a new keyboard language is installed
When the keyboard is removed (the Programmer has been previously turned ON with a keyboard)
When a keyboard has been added (the Programmer has been previously turned ON without a keyboard)
When the PC card has been removed (the Programmer has been previously turned ON with a PC card)
When a PC card has been added (the Programmer has been previously turned ON without a PC card)
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Troubleshoot potential interference
To address possible harmful interference between the Programmer and other devices, you are encouraged to take one or more of the following measures to address the situation:
Reorient or relocate the devices.
Increase the separation between the devices.
Connect the equipment to an outlet on a different circuit.
Consult Medtronic or Vitatron for help.

Connect peripheral devices

An analog input/output connector under the keyboard allows the use of a peripheral isolated medical grade recorder or monitor. A special adapter accessory (not included with the Programmer) is needed to use the input/output connector. Contact your Medtronic or Vitatron representative for more information. The signals present at the output depend on the software application, but may include the following:
ECG
Marker Channel telemetry
EGM
Software specific waveforms
Set up the Programmer
Connect peripheral devices
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All electronic devices that are connected to the Programmer must meet the electrical safety requirements of IEC-60950-1.
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Chapter 2
Connect peripheral devices
Locate the peripheral device connector
1 Analog Input/Output connector with green marker (under
the keyboard)
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Conduct a patient session3

Prepare for a patient session 40
Initiate a patient session 51
End a patient session 55
Store components 56
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Chapter 3

Prepare for a patient session

Prepare for a patient session
Familiarize yourself with the following information before beginning a patient session:
Connecting the Programmer to skin electrodes
Using the touch pen
Using the keyboard
Positioning the programming head
Emergency VVI button
Connect the Programmer to skin electrodes
At the start of each patient session, ECG cable leads must be connected to the patient to detect cardiac and pulse artifact signals.
Note: The quality of disposable skin electrodes used with the Programmer is important to the performance of the Programmer signal sensing functions. Chemical reactions occur at the electrode/paste interface and produce small DC voltages that can block the ECG signal. Using high quality silver/silver chloride (Ag/AgCl) electrodes can minimize this problem. Electrodes should be fresh and from the same box. The patient’s skin should be prepared according to the directions provided with the electrodes.
Protocols covering attachment of leads to disposable skin electrodes may vary. Leads may be attached to the electrodes either before or after the electrodes are applied to the patient. The order of the procedure given below is arbitrary.
Warning: Do not connect the Programmer to wires or electrodes internal to the body. The Programmer is designed to be medically safe only when attached to surface electrodes.
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Attach electrodes
R N C F L
RA RL V LL LA
Connect the ECG cable
Conduct a patient session
Prepare for a patient session
1. Attach five standard, disposable electrodes to the patient in the positions shown.
1. As shown, attach a color-coded lead wire to each of the five electrodes. Match a color to each electrode as in Table 3-1. Note: Connecting the chest lead is optional. If the chest lead is not used, insert the chest ECG plug into the middle cable port of the ECG cable.
2. Connect each lead wire to the ECG cable as in Table 3-2. Match each lead connector to the proper cable port.
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Tab le 3- 1. Electrode lead wire color coding
AHA Coding
Black Yellow to left arm
Red Green to left leg
Brown White to left chest area
Green Black to right leg
White Red to right arm
a
American Hospital Association
b
International Electrotechnical Commission
c
Connecting the chest lead is optional. If the chest lead is not used, insert the
chest ECG plug into the middle cable port of the ECG cable.
Tab le 3- 2. ECG cable color coding
AHA Coding IEC Coding
Black to LA Yellow to L
Red to LL Green to F
Brown to V
a
a
IEC Coding
b
Body Area
White to C
c
Green to RL Black to N
White to RA Red to R
a
Note: Occasionally, mutual interference occurs between the Programmer skin electrode signals and signals from an external ECG recorder or monitor attached directly to the patient. This interference may cause erratic operation of the Programmer functions that depend on surface signal detection. If interference occurs, the leads from the attached ECG recorder or monitor should be temporarily disconnected. This interference does not affect the programming functions of the Programmer.
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Labeled C on some cables
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Use the touch pen
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V
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Conduct a patient session
Prepare for a patient session
The touch pen is used to select programming functions provided by the software. Proper use of the pen is described below in Figure 3-1 and in “Select an option on the screen” on page 44.
Figure 3-1. Using the touch pen
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Prepare for a patient session
Select an option on the screen
1. Move the tip of the pen to a position directly over the desired option
While positioning the pen, do not press it against the screen. Hold the pen perpendicular to the screen. The pen tip should be close to the screen. If the desired option is a displayed key or button, position the pen tip within the rectangular outline.
If the desired option is a name or number, such as a parameter or parameter value, position the pen directly over the letters or numbers forming the option.
2. Touch the pen to the screen to select
an option.
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Use the keyboard
Conduct a patient session
Prepare for a patient session
Certain fields on the screen allow you to enter data, such as the patient’s name or chart number. The Programmer has a compact computer keyboard for entering data.
Figure 3-2. Programmer keyboard
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Position the programming head
At some point during most applications of the Programmer, the programming head must be positioned over the implantable device. Positioning the programming head is required for any interaction between the Programmer and the implantable device.
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Chapter 3
Prepare for a patient session
When to position the programming head
Caution: Do not position the programming head over an
implanted device during electrocautery or external defibrillation procedures.
During a patient session, properly position the programming head over the implanted device before any of the following actions:
Selection of any command that initiates a programming transmission. The programming head must be held in position until completion of the transmission, which is usually indicated by a confirmation message.
Selection of any command that initiates data transmission from the implantable device. The programming head should be held steady until data reception is complete, which is usually indicated by a confirmation message.
Selection of a measurement function that requires the implantable device to be operating asynchronously as a result of the programming head magnet.
For any temporarily programmed state or function or for reception of continuous data such as Marker Channel telemetry or EGM waveforms, the programming head must be held in place over the implantable device for the duration of the function or until termination is desired. Lifting the programming head cancels a temporary program and terminates continuous telemetry. The implantable device reverts to permanently programmed values.
Determine the correct position
For an implantable device, the programming head should be held directly against the patient’s skin. The face of the programming head must be parallel to and typically within 5 cm of the implantable device. Optimum position of the programming head may not be directly centered over the implantable device.
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Conduct a patient session
Green
Amber/Green
Light Array
Prepare for a patient session
Figure 3-3. Positioning the programming head
Correct placement of the programming head is indicated in two places: the position head array in the top left corner of the screen and the array of seven lights on the programming head (see Figure 3-3).
Programming and Interrogation are not recommended when fewer than two green lights are on.
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Program and interrogate the implanted device
1. Select the appropriate software parameters according to the reference guide.
2. Position the programming head near the implantable device.
Programming and Interrogation can begin when the LED lights on the position head array indicate satisfactory positioning and telemetry strength.
Notes:
For Medtronic devices, the programming head array shows the signal strength of the communication link. Medtronic recommends moving the programming head to maximize the number of green lights. All lights may not illuminate for all models (see the reference guide for the implanted device).
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I
P
Chapter 3
Prepare for a patient session
Use the P and I buttons
Misalignment of the programming head could result in failure of a programming transmission and/or failure to receive data from the implantable device. Medtronic recommends that you interrogate the device after programming to confirm that any setting changes were successful.
Reveal Plus and some older Vitatron devices respond with only one light in the position head array. In programming mode, the light turns green, to indicate that the programming head is in the correct position and that it is communicating with the device; the light turns solid amber if the programming head is misaligned.
The P button and I button on the programming head (Figure 3-4) correspond to commands that appear on the display screen of the Programmer. Refer to the appropriate reference manual to determine which commands the buttons correspond to. For convenience, you may press the P button or the I button on the programming head in place of selecting the corresponding option from the display.
Figure 3-4. P and I buttons
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The programming head magnet
A strong magnet in the programming head actuates a sensor in the implantable device, which makes the implantable device receptive to programming (refer to the reference guide for the implanted device for more information about the effects of a magnet).
Be aware that the programming head may attract metal instruments or be attracted to metal surfaces. The magnet is susceptible to partial demagnetization when it is subjected to opposing magnetic fields, such as those present when forcing the programming head against another magnet. The programming head should be stored as shown in Figure 3-6 on page 56 when not in use.
Caution: Keep the programming head away from any device or material that will be damaged by the magnetic field, including computer diskettes.
Emergency VVI button
The red Emergency VVI button on the display panel provides immediate access for emergency VVI pacing (Figure 3-5). (Specific parameter values are determined by each application.)
For all Medtronic pacemaker applications, the red Emergency VVI button is active when the [Emergency] button is displayed on screen.
For some ICD applications, the red Emergency VVI button is active at all times. When pressed, this button delivers VVI pacing and displays the emergency screen options.
Conduct a patient session
Prepare for a patient session
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Note: The red Emergency VVI button is also implemented in the software and appears on the display. It functions similarly to the button on the panel.
Warning: The red Emergency VVI button is disabled for the following devices: PCD, Jewel PCD, Micro Jewel II, MicroJewel, Jewel CD, Jewel Plus, Model 7202 Jewel CD, Models 7218 and 7211, Model 7201 CD, and Jewel AF. Use the touch pen to select the on-screen [Emergency] button.
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VVI
Emergency VVI
Button (Red)
Chapter 3
Prepare for a patient session
Deliver emergency bradycardia pacing
To initiate emergency pacing, correctly position the programming head over the implanted device and press the red Emergency VVI button. A message confirms programming, and emergency VVI operation begins.
Deliver emergency tachyarrhythmia therapy
To deliver therapy, press the red Emergency VVI button to display the emergency screen on the Programmer and select the on-screen [Deliver] button with the touch pen.
For specific applications, refer to the appropriate device Reference Guide, System Reference Guide, or Clinician Manual for complete instructions regarding the use of the Delivery button.
Figure 3-5. Emergency button
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Initiate a patient session

A patient session involves the application of the various Programmer functions to such procedures as programming implantable device parameters, analyzing or assessing implantable device operation, troubleshooting, and routine follow-up. The instructions for using each Programmer function are covered in the reference guide for the implanted device.
Note: Before proceeding, ensure that all preparations covered in Chapter 2, “Set up the Programmer” on page 31 and “Prepare for a patient session” on page 40 have been completed.
Programmer checklist
1. Is the Programmer set up according to the procedures in Chapter 2?
2. Are the ECG cable, touch pen, and programming head connected to the Programmer?
3. Does the power cord connect the Programmer to an AC power outlet?
4. Has the appropriate software been installed? Refer to Chapter 6 for a description of how to verify the software version.
5. Are the Programmer ECG cable leads connected to electrodes on the patient as described in “Connect the Programmer to skin electrodes” on page 40?
Conduct a patient session
Initiate a patient session
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Specific information related to each implantable device model or family of models is included in the reference guide for the device.
Refer to the reference guide for the implanted device before beginning a patient session.
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Model identification
Because the Programmer collects and stores data on a session-by-session basis, it is important to correctly start and end each session.
The Programmer supports both a Medtronic and Vitatron desktop. Whichever desktop is in use when the Programmer is powered down, that same desktop will appear when the Programmer is powered on. To switch from the Vitatron desktop to the Medtronic desktop and vice versa, select the Vitatron/Medtronic switch button that appears on the bottom of the screen.
There are two ways to begin a patient session:
Prior to turning on the Programmer, position the programming head over the patient’s device. When you turn on the Programmer, the Programmer will attempt to interrogate the device. Depending on the device, either the software application will be launched automatically or a message will appear with further instructions.
After turning on the Programmer, position the programming head over the patient’s device. During the first 5 minutes, the Medtronic desktop will display the Find Patient screen. Afterward, it displays the Select Model screen. The Vitatron desktop displays the Select Model screen immediately. A patient session can begin at either the Find Patient screen or the Select Model screen. Follow the instructions on the screen that displays.
Find Patient screen
When the Programmer is first turned on, the Medtronic desktop displays the Find Patient screen. If it does not detect a device within about 5 minutes, the Programmer removes the Find Patient screen to reveal the Select Model screen.
When the Find Patient screen is displayed, you may begin a patient session.
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Conduct a patient session
Initiate a patient session
Place the programming head over the patient’s device and hold it steady. For most devices, the Programmer will identify the device model and automatically start up the proper software application. If a device cannot be automatically identified, the Programmer displays a message at the top of the Find Patient screen. Perform one of the following steps, depending on the message instructions:
Select [Cancel] and manually select the software application from the Select Model screen.
Select [Cancel] and then select the Vitatron/Medtronic switch button to go to the Vitatron desktop.
If the message indicates that the needed software application has not been installed, contact your Medtronic or Vitatron representative.
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Select Model screen
A patient session may also begin from the Select Model screen. The Select Model screen appears after one of the following actions:
If the Select Model screen is not displayed, use the touch pen to select the Select Model icon. If the Select Model icon is not displayed, a patient session is in progress. You must end that session before starting a new one.
If you are between patient sessions, you can access other screens by using the icons and buttons described in Chapter 5.
Shortly after the Programmer has been turned on
After you end a patient session
If the device is a Vitatron device and it is not listed on the Select Model screen, refer to the Vitatron Software Programming Guide.
If the Select Model screen does not look like this example and you see a button, select the Vitatron/Medtronic switch button to display this screen.
Position the programming head over the patient’s device and hold it steady. Select [Find Patient] shown on the Medtronic desktop or manually select the device from the displayed list of devices and select [Start].
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Conduct a patient session

End a patient session

When a device is manually selected from the list of devices, the Programmer starts up the application that corresponds to your selection, not the device that is under the programming head. The Find Patient screen quickly displays as the Programmer starts up the proper software application.
If the software application has not been installed, the Programmer displays a message indicating the software needs to be installed before proceeding.
The Programmer may automatically interrogate the patient’s implanted device to retrieve most of the data that might be needed during the session. To take advantage of this automatic interrogation, you must position the programming head over the implanted device and continue to hold it in place until the interrogation is complete.
Refer to the reference guide for the implanted device for more information about determining the model.
Note: If you are using the optional Analyzer and your device does not support concurrency, you must exit the Analyzer before you can start a device session. That is, if you use the task bar to switch from the Analyzer to the Select Model screen and then select [Find Patient], the Programmer will display the message:
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This application is not able to run concurrently with the Analyzer. Please exit the Analyzer and try again.
End a patient session
When you want to end a patient session, you may save data to a supported storage device or end the session without saving.
Please refer to the reference guide for the implanted device for specific information on saving device data.
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Store components

Store components
The following diagrams show the proper way to store components (Figure 3-6).
Figure 3-6. Storing components
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Manage reports and data4

Reports 58
Session data 58
Save to a PDF file 58
Save to diskette 59
Save to USB 59
View reports that are saved to media 61
Vitatron Manual-Guided Reset 62
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Chapter 4

Reports

Reports

Session data

Depending on the implanted device model, various types of reports can be created. Refer to the reference guide for the implanted device for specific information on report types and contents. During an active session, reports may be printed, or saved as PDF files on a diskette or USB flash drive. Reports held for later printing may be printed while at the Desktop or when returning to a session. Note that reports might not be available for later printing from the Desktop, depending on the device application and on the current print queue deletion schedule (see “Set the interval for report deletion” on page 75).
Patient session data may be saved to a diskette or a USB flash drive.

Save to a PDF file

Printable reports, frozen strips, and other data may be saved to a PDF file. A PDF file is an electronic version of a printed document; therefore, the feature is accessible under the printing commands.
Note: The Save to PDF File feature will work for all applications that can print to a full-size printer.
To save to a PDF file, perform the following steps:
1. Open or create the report or file.
2. Select [Print...] or [Print Options...] to display the
3. From the Print – Options dialog box, select the Printer: Full
Programmer Reference Guide
Print - Options dialog box.
Note: If the Print – Options dialog box does not display, open Preferences, and select the Printing: Pop up these options when any Print button is selected check box.
Size radio button. A list of supported printers is displayed.
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Save to diskette

Refer to the reference guide for the implanted device for specific information on saving and reading device data using a diskette. The diskette drive is functional only when a USB flash drive is not in use. Before using the diskette drive, ensure that a USB flash drive is not connected to the Programmer.
When no USB flash drive is connected, the diskette indicator is green to indicate that the diskette drive is available for use. Inserting a diskette allows all session data and PDF file saving operations to take place on the diskette.
Manage reports and data
Save to diskette
4. From the list of printers, select the Save to PDF File option. The report is saved to an attached USB flash drive, or to a diskette, if one is present in the diskette drive and a USB flash drive is not connected. Refer to “Saving to USB” for further information.
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Save to USB

Many device applications support the use of diskettes for saving and loading session data. The Programmer is also able to perform these operations using a USB flash drive. When a USB flash drive is connected to the Programmer, the diskette drive becomes unavailable.
Note: Device applications and reference manuals may still use the terms “disk” or “diskette” in the context of saving and retrieving device data. When a USB flash drive is connected to the Programmer and available for use as described below, the terms disk or diskette should be interpreted as applying to the USB flash drive, rather than the diskette.
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Save to USB
Supported USB storage devices
Storage of device session data and PDF reports from the Programmer is supported only with USB flash drives. In order to ensure the integrity and security of patient health information, it is recommended that you use USB flash drives that are dedicated to storing Programmer data only.
Operation
A USB flash drive should be connected or disconnected while at the Desktop or in a session. Connect a writable USB flash drive to the Programmer using any available USB port. A slight delay may occur while the USB flash drive is authorized. The USB indicator on the task bar turns green to indicate that the USB flash drive is available for use, and the diskette icon turns gray to indicate that the diskette drive is not available.
USB flash drives should not be connected or disconnected while the following actions are in progress:
Programming a device
Performing a Save to Disk
Performing a Read from Disk
Saving a report as a PDF file
Notes:
Programmer Reference Guide
While a Save to Disk action is in progress, the progress indicator and the message “Saving...” display. The progress indicator displays the completion percentage. Before removing the USB flash drive, wait a few seconds after the progress indicator shows 100%.
After a report is saved as a PDF file, the message “PDF report(s) saved to media” displays for about 5 seconds. Wait a few seconds after the message goes away before removing the USB flash drive.
If an active session is ended while reports are currently printing or pending, the reports will be cancelled and may not be available from the Desktop print queue.
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View reports that are saved to media

Any operation that normally uses a diskette to read or write data (such as Save to Disk, Read from Disk, save reports to a PDF file) will use the USB flash drive after it is connected. Refer to the reference guide for the implanted device for specific information on saving device data. See “Saving to a PDF file” for more information on saving reports to PDF files.
Connect only one writable USB flash drive at a time. Connecting two or more USB flash drives will result in an error during data-saving operations. This condition is indicated by the USB disabled icon.
View reports that are saved to media
Reports that have been saved to media may only be viewed on a computer; they cannot be viewed on the Programmer itself. After saving, remove the storage media (diskette or USB flash drive) containing the reports and insert it into a computer equipped to display files that are in PDF format.
Manage reports and data
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All reports from one patient's session are contained in one PDF file. File names are automatically assigned according to a naming convention that ensures uniqueness on the storage media:
Patient's name (if previously provided in Patient Information)
Device serial number
“Session Report”
Clinic visit date in MM_DD_YY format
Version number (the first PDF saved to this storage media gets “1”)
For example: John Q Patient_aaannnnnna_Session Report_06_25_10_1.PDF
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Vitatron Manual-Guided Reset

Recommendations for viewing and printing PDF files
Due to computer and software variations, some PDF files may not display properly when viewed on a computer monitor.
The use of Adobe Reader 9 or later is recommended. Adjusting the following settings may reduce or eliminate display imperfections:
Replace document colors with white page background and black text (in Adobe Reader 9, select: Edit | Preferences… | Accessibility | Custom Color)
Deselect the option to enhance thin lines (in Adobe Reader 9, select: Edit | Preferences… | Page Display)
Imperfections that may be seen on screen:
On graphs that contain rectangles drawn with thin lines, e.g., bar graphs, the thin lines may not display at various zoom levels.
On Pacing and Tachy Trigger Episode reports, unfilled circles may display as filled circles.
PDF reports will print properly at a resolution of 300 dpi or greater.
Vitatron Manual-Guided Reset
Manual-guided reset is a diskette-based tool that allows recovery of Vitatron DDD3, DIVA, and (Co)DEMA devices that have lost data such as losing trim values on a device reset. Before attempting to use the MGR diskette, ensure that no USB flash drives are connected.
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Use external printers 64
Install printer paper 67
Printer buttons 68
Tear off a printout 69
Low paper supply 69

Use printers5

5
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Chapter 5

Use external printers

Use external printers
Connecting a compatible printer to the Programmer allows you to print full, page-size reports of session data when available (see the reference guide for the implanted device). This section describes how to connect a printer to your Programmer.
All printers listed by this software are certified to IEC 60950, UL 60950 or equivalent. Only printers listed by this software may be connected to the Programmer.
Printer compatibility
The Programmer is compatible with many printers. A list of compatible printers can be accessed from the Print Queue screen.
Note: When programming a Vitatron device, refer to the applicable Vitatron reference guide for information about the print queue.
View a list of supported printers
Some devices only support the internal Programmer printer. In these cases the Print Queue window will not display during a session; it will display from the desktop when not in a session. Refer to the applicable device reference guide.
For those devices that support an external printer, refer to the following procedure.
Programmer Reference Guide
1. If you are conducting a patient session, select
Reports then Print Queue.
If you are not conducting a patient session, select the Print Queue icon.
2. On the Print Queue screen, select the Printer field to open the list of supported printers.
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Use printers
2
Use external printers
Materials you will need
To connect a printer to the Programmer, you will need a USB printer cable or a Parallel Interface printer cable. For a USB printer cable, one end must be a USB Type A connector. The other end of the cable must fit the USB port on your printer. For a Parallel Interface printer, one end of the cable must fit the parallel interface port on your printer. The other end of the cable must be a standard 25-pin male D connector.
Connect the printer
Prior to connecting a printer to your Programmer, you should exit the patient session and turn the Programmer off.
To connect the printer to your Programmer (method you use depends on your Programmer hardware)
The following steps apply to Programmers that support both parallel and USB printing.
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1. To connect a printer, locate the correct port.
For USB cable printers, use a USB port located in the power cord compartment of the Programmer.
For Parallel Interface printers, the Parallel Interface port is located under the disk drive/PC card cover on the right side of the Programmer. Open the cover by pushing down on the small latch at the top center of the panel.
2. Connect the printer cable to the USB port or parallel connector on the Programmer.
3. Connect the other end of the cable to the printer. Connect the printer power cord to an outlet and turn the printer on. Make sure that the printer has paper. Note: Refer to the technical information provided with your printer for information about connecting and operating the printer.
4. Turn the Programmer on and select the Print Queue icon. Note: Be sure to select the correct printer driver from the options
listed when you select the Printer field on the Print Queue window. You are now ready to use your Programmer with the connected printer.
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Use external printers
The following steps apply to Programmers with hardware that supports only USB printing.
1. To connect a printer, locate the correct port. There is one USB port located under the disk drive/PC card cover and two ports located under the power cord door on the back of the Programmer.
2. Connect the printer cable to a USB port on the side or back of the Programmer.
3. Connect the other end of the cable to the printer. Connect the printer power cord to an outlet and turn the printer on. Make sure that the printer has paper. Note: Refer to the technical information provided with your printer
for information about connecting and operating the printer.
4. Turn the Programmer on and select the Print Queue icon. Note: Be sure to select the correct printer driver from the options
listed when you select the Printer field on the Print Queue window. You are now ready to use your Programmer with the connected printer.
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Install printer paper

The internal printer requires a special thermal paper supplied in flat packs. You may obtain this paper directly from Medtronic or Vitatron. One package of printer paper contains six individual packs of paper. Each pack contains approximately 200 perforated sheets.
How to load printer paper
Use printers
Install printer paper
1. Press the latch on the top of the tray on the left side of the Programmer. Slide the tray out. Flip the paper holder over the end of the tray and remove any remaining paper. Note: The tray may be taken out of the Programmer to make
removing any remaining paper easier. Press down on the lever on the side of the tray toward the front of the Programmer.
2. Remove the wrapping from a new flat pack of printer paper, dispose of the cardboard and unfold the top sheet.
Note: The shiny side of each sheet of paper with two black squares should be facing up as the paper is loaded into the tray. The black squares must be positioned toward the front of the Programmer.
3. Slide the paper pack toward the back of the tray. Flip the paper holder over the paper pack.
4. Fold the top sheet of paper over the paper holder. Slide the tray back into position.
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3
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Chapter 5

Printer buttons

Printer buttons
The four buttons shown below control certain printer functions.
Figure 5-1. Printer buttons
150 mm/s
225 mm/s
3 12.5 mm/s
4 Paper Advance
50, 25, or 12.5 mm/s. – Three buttons allow for selection of a desired paper speed for ECG, Marker Channel telemetry, and EGM recording. Pressing a button selects the printer speed and turns on the indicator light. Pressing a lit button stops the printout. The selected paper speed is printed once along the top edge of the chart recording. Paper speed for text printing is not affected by these buttons.
Paper Advance – Pressing Paper Advance advances the printer paper to its next perforation for tearing off.
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Tear off a printout

When you wish to tear off a printout, separate the paper strip at a perforation. To tear the printout off at the printer, press Paper Advance. This action advances the paper to the next perforation. Grasp the printout near the printer, and pull.
Figure 5-2. Tearing off printouts
Use printers
Tear off a printout
69

Low paper supply

As the paper supply nears its end, a red stripe will appear along the edge of the paper. At this point, a new paper pack should be installed as previously described in this chapter. When the paper supply runs out, the printer stops operating.
Note: The thermal paper used in this Programmer is intended for immediate use. As the quality of thermal paper diminishes over time, the image fades. Medtronic and Vitatron recommend that you make photocopies for your files.
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Select options6

About the between sessions tool palette 72
Adjust Programmer time and date 73
Select audible tones 74
Set the interval for report deletion 75
Manage patient data privacy 76
Change the language setting 79
Improve the detection of pacing artifacts 79
Check the software version 80
Start the demonstrations option 81
View and update Programmer location and hardware information 81
Select other software 83
Remove other software applications 83
6
Obtain technical manuals 84
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Chapter 6

About the between sessions tool palette

About the between sessions tool palette
The between sessions tool palette is on the Select Model screen.The Select Model screen appears before you select a model, when you turn the Programmer on, and when you end a patient session.
The tools that are available between sessions are described in Ta bl e 6 - 1 .
Note: When programming a Vitatron device, refer to the applicable reference guide for information about the tool palette.
Tab le 6- 1. Between Patient Sessions tool palette
Tool palette Tool Selecting the tool (button or icon)…
Freezes a segment of the live rhythm display. Note: A frozen strip can be viewed, printed, or saved to PDF
(but not saved to diskette) between patient sessions. Markers and EGM traces are not present between patient sessions.
Accesses the rhythm strips saved during a patient session. Note: No saved strips are available between patient sessions.
Programmer Reference Guide
Opens a window of options for adjusting the live rhythm display. Note: Additional adjustment options are present during a
patient session.
Displays the screen for selecting a model and starting a patient session.
Displays a queue of print requests from previous sessions as well as frozen waveform reports requested between sessions. Refer to the reference guide for the implanted device to determine if these features are available.
Displays the Programmer setup options.
Preferences Time and Date Artifact Detection Software Demonstrations Programmer Profile Other Software
Selects the Analyzer for analyzing the electrical performance of a cardiac lead system (requires optional hardware - see the 2290 Analyzer Reference Guide.)
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Note: When some functions are active on the display, selecting a tool button or icon will have no effect. Closing the active window restores operation of the tool palette.

Adjust Programmer time and date

If the time or date displayed and printed by the Programmer is incorrect, use the following procedure to enter the correct settings. For Vitatron devices, see the applicable reference guide.
Set the time and date
1. Select Programmer then Time and Date.
2. From the Programmer Time and Date screen, select the or button to increase or decrease the value for the unit of time
you want to change. Press and release the button for single unit changes or press and hold the button to effect greater changes.
3. When all fields show the correct time and date, press [Apply].
Select another tool palette icon to close the Programmer Time and Date window.
Select options
Adjust Programmer time and date
73
Figure 6-1. Programmer Time and Date screen
Note: Time must be entered on the basis of a 24-hour clock,
with 00:00 being midnight and 12:00 being noon.
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Chapter 6

Select audible tones

Select audible tones
Turn tones on or off
Certain events in the operation of the Programmer result in an audible signal. The following tones alert the user to the success or failure of an action.
A two-tone beep (low-to-high) indicates confirmation of an Interrogate or a Program command.
A double low-tone beep indicates that an Interrogate, Program, or Emergency command was not confirmed. It can also indicate that the selected command cannot be executed.
Note: For some devices, the tones may not be turned off. See the reference guide for the implanted device. For Vitatron devices, see the applicable reference guide.
1. Select Programmer then Preferences.
2. From the Preferences screen, select [Audio ON] or [Audio OFF] as desired.
Figure 6-2. Audio Preferences screen
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Set the interval for report deletion

For patient data security, the Programmer permanently deletes reports automatically from the Medtronic desktop print queue at the time when the Programmer is powered up. You can control how long reports are retained in the print queue before automatic deletion.
Select a report deletion interval
1. Select Programmer then Preferences.
2. From the Preferences screen, select Delete Reports.
The Programmer displays the screen shown in Figure 6-3.
Figure 6-3. Delete Reports screen
Select options
Set the interval for report deletion
75
3. Click a radio button to specify which reports the Programmer deletes:
All Reports
Reports older than 1 Day
Reports older than 2 Days
Reports older than 7 Days (Default)
Reports older than 14 Days
The age of a report is determined by the date and time it was created. When the Programmer is powered on, reports that meet the deletion criteria are permanently deleted.
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Manage patient data privacy

Delete a report immediately
To delete a report immediately, directly access it from the print queue and click Delete.
Manage patient data privacy
You can immediately remove from the Programmer all Protected Health Information (PHI). This feature deletes all of the following files:
Contents of the Print Queue (unless files are currently being printed or copied)
Temporary files residing on the Programmer
Memory dumps (applies to Vitatron devices only)
You cannot delete any PHI data if a session is in progress or while files are being printed or copied to media. If deletion is interrupted manually, some PHI will remain on the Programmer.
Note: The Programmer user is responsible for the use of this feature, as well as for management of patient data that has already been removed from the Programmer (for example on paper, diskette, or a USB flash drive).
Delete Protected Health Information
1. Select Programmer then Tools. The Programmer displays the screen shown in Figure 6-4.
Figure 6-4. Tools screen with Patient Data Privacy index item selected
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Select options
Manage patient data privacy
2. Click Delete Protected Health Information. The Programmer displays the screen shown in Figure 6-5.
Figure 6-5. Delete Protected Health Information confirmation dialog box
3. Click Delete to continue.
One of the following events may occur:
The Programmer displays an “In progress...” popup screen as shown in Figure 6-6. Deletion may last several minutes, depending on the amount of data to delete.
Figure 6-6. “In progress...” popup screen
77
Note: On the “In progress...” popup screen, click Stop if you wish to halt further deletion. For example, you may want to end a deletion process that is taking too long.
Be aware that if you click Stop, some PHI will remain on the Programmer.
Or,
If there are reports currently printing, the Programmer displays a message as shown in Figure 6-7, directing you to wait until printing is complete. Click Close.
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Manage patient data privacy
Figure 6-7. Printing in progress dialog box
4. If clicking Delete in Step 3 resulted in PHI deletion, the Programmer displays a message stating that deletion was successful (Figure 6-8). Click Close.
Figure 6-8. Deletion successful dialog box
Or,
If the Programmer is unable to complete deletion of files, it displays a message stating that there was an error and that some data may remain on the Programmer (Figure 6-9). Click Close. Contact Medtronic Technical Support if the message recurs.
Figure 6-9. Error deleting files dialog box
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Change the language setting

Change the language setting
The software is translated into several languages. Use the following procedure to determine which languages are available. For Vitatron devices, see the applicable reference guide.
Choose a language
1. Select Programmer then Preferences.
2. From the Preferences screen, select the Language field to display the options.
Note: The Programmer screen goes blank for about 2 minutes after selecting a language. The Programmer will then resume operation in the selected language.

Improve the detection of pacing artifacts

Select options
79
The Artifact Detection function allows one to improve the detection of pacing artifacts when interference causes either false artifacts or no artifacts to appear on the patient’s ECG. Pacing artifacts are displayed on the patient’s ECG when the artifact detection option (Show Artifacts) has been enabled.
See the reference guide for the implanted device to determine if this feature is applicable.
Enable artifact detection
1. Select Programmer then Artifact Detection.
2. Make sure current settings include ARTIFACT DISPLAY IS ON.
3. Make sure current settings include MV FILTER IS ON.
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Check the software version

Check the software version
This section describes how to determine the version of software that is loaded on the Programmer.
If you need to know what version of software is currently loaded on the Programmer for any of the device models, use the following procedure.
For Vitatron devices, see the applicable reference guide.
To check the software version number
1. Select Programmer then Software.
2. For each device model with software loaded on the Programmer, the screen displays the software version number next to the model number.
Figure 6-10. Software on This Programmer screen
Note: If the model that you require is not displayed, the software
to support that model is not currently loaded on the Programmer. Contact your Medtronic or Vitatron representative.
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Start the demonstrations option

The demonstrations option allows you to run a demonstration program on the Programmer.
For Vitatron devices, see the applicable reference guide.
Note: Device applications and reference manuals may still refer to using the “demonstration disk” or “demonstration diskette” to run a demonstration program. The need for a demonstration diskette to access demonstration mode is no longer required. All references to a demonstration diskette can be ignored. If a demonstration diskette is inserted inadvertently, operation of the demonstration mode is not affected. All demonstration mode features are accessible with or without a demonstration diskette.
Access demonstrations
1. Select Programmer then Demonstrations.
2. From the Demonstration Model Selection screen, select the desired View option to list the available demonstration programs.
3. Select the desired demonstration program and press [Start] followed by [Continue].
Select options
Start the demonstrations option
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View and update Programmer location and hardware information

Information about the location of the Programmer and its hardware is on the Programmer Profile screens.
The Programmer Profile location screen has the following information:
Clinic’s name, address, phone number, contact person, and customer account number
Service representative’s name, phone number, fax number, and e-mail address
The Programmer Profile hardware screen has the model number for the Analyzer, and model and serial numbers for the Programmer and the programming head.
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View and update Programmer location and hardware information
Information on the screen may be updated by selecting the appropriate field and then using the keyboard.
Access Programmer Profile screens
1. Select Programmer then Programmer Profile. Location information appears by default.
2. To view hardware information, select Hardware Information.
Verify Programmer Profile information
Each Programmer has a profile screen that contains identifying information about the installed hardware, the Programmer location and contact information for the Medtronic service representative.
Typically, the profile is completed when the Programmer is first installed and then updated only when necessary.
1. Select the Programmer icon and then select Programmer Profile.
2. Complete the location information or verify that the information shown is correct.
Figure 6-11. Programmer Profile screen
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Select other software

In addition to the standard application software, there are some Programmers that have special applications installed. These special applications are considered research software and are used in conjunction with clinical studies. If you have this research software installed, you may access the software, using the following procedure.
1. Select Programmer then Other Software.
2. When the Programmer displays the list of available software, select the application and press Start.

Remove other software applications

Programmers with special applications installed, such as those used in clinical studies for research, may allow the applications to be removed from the Programmer desktop. If you have software installed that permits removal, you may remove it using the following procedure.
Select options
Select other software
83
1. Select Programmer then Software.
2. Press Uninstall Software...
3. When the Programmer displays the list of removable software, select the application to be removed, and then press Uninstall.
4. Select the check box next to the acknowledgement statement, and then press Continue.
5. The software is removed, and the Programmer reboots.
6. Verify that the software has been removed.
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Chapter 6

Obtain technical manuals

Obtain technical manuals
Medtronic technical manuals, including the one you are reading, are available in a number of different formats from the Medtronic eManuals web site listed on the back cover of this manual. The web site offers real-time access to the latest version of manuals 24 hours per day, seven days per week. Manuals can be viewed online, downloaded for viewing or printing, or ordered from the web site.
All manuals are available online in English. Most manuals are also available in additional languages in online, CD-ROM, or paper format. New manuals are added to this site regularly. If you do not find the manual you want, please contact your Medtronic or Vitatron representative.
Your order for CD-ROM or printed versions of manuals will ship from our facility within 24 hours and should reach you within 3 business days. If you need a copy before the shipment arrives, download the manual and print it, or contact your Medtronic or Vitatron representative.
Access the eManuals web site
1. Point your browser to the web site listed on the back cover of this manual
2. Make location and language selections, and click OK.
3. To see lists of CRDM manuals, click on the desired category on the left of the screen. You can also search for manuals using a product name or model number.
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Service the Programmer7

Clean the system components 86
Sterilize the programming head, ECG cable, and lead wires 86
Replace a PC card 87
Programmer specifications 88
Special notice 91
Medtronic limited warranty 92
7
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Chapter 7

Clean the system components

Clean the system components
The exterior surfaces of the Programmer and its accessories may be cleaned with a damp sponge or soft cloth moistened with water, mild detergent, or alcohol. Thoroughly clean the surfaces of the Programmer wires; the bottom surface of the Programmer wand; and the wire connecting the Programmer wand to the Programmer.
Caution: Take care to prevent liquid from entering the Programmer and programming head. Do not immerse the Programmer or any accessories in any liquid or clean them with aromatic or chlorinated hydrocarbons.
With the exception of the programming head and ECG leads and cable, the Programmer and its accessories cannot be sterilized.

Sterilize the programming head, ECG cable, and lead wires

Caution: Do not autoclave the programming head or ECG cable
and lead wires.
Ethylene-oxide
Note: The programming head or ECG cable and lead wires must
be completely dry before being ethylene-oxide sterilized.
Biological indicators should be used to ensure that proper sterilization standards have been met. A previously validated sterilization cycle should be used.
Due to the variability in sterilization systems, precise sterilization instructions cannot be provided. Contact the manufacturer of your sterilization system for more information regarding procedures.
Programmer Reference Guide
1. Wrap the programming head or ECG cable and lead wires in packaging permeable to ethylene oxide.
2. Medtronic recommends that exposure to ethylene oxide is not to exceed 3 hours and is followed by a minimum of 12 hours of aeration.
3. Do not exceed 55 °C.
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Service the Programmer

Replace a PC card

Gas plasma (programming head only STERRAD 100S gas plasma system)
1. Place the programming head in packing material appropriate for gas plasma sterilization.
2. Sterilize by procedures validated for effectiveness using suitable biological controls. a. Do not exceed 55 °C. b. Do not use an H2O2 concentration below 1 mg/L. c. Do not expose the programming head to a sterilizer cycle longer
than 72 minutes.
d. Do not resterilize more than five programming heads in one load
or combine them with other surgical instruments or devices in the same load.
Visually inspect the cable and connections of the programming head after sterilizing. Do not use the programming head if it appears damaged. Damage includes, but is not limited to deterioration of the cable insulation (brittleness, cracking, thinning, or bare spots). Do not use the programming head if the conductive wires are exposed.
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Replace a PC card
Contact your Medtronic or Vitatron representative if you need to replace a PC card in the Programmer.
Note: It is not necessary to perform a safety check when a PC card is inserted or replaced in the Programmer.
Procedure for replacing a PC card
1. Turn off the Programmer.
2. Open the disk drive/PC card cover. See Figure 1-5 for the location.
3. Remove the existing PC card.
4. Insert the new PC card.
5. Turn on the Programmer.
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Chapter 7

Programmer specifications

Programmer specifications
Tab le 7 -1. Programmer specifications
Standards (The Programmer complies with the following:)
EMC Patient Safety
Voltage
Frequency Power
Electrical safety requirements per IEC 60601-1 clauses 18 and 19
Impedance between earth connection and housing
Enclosure leakage current
Earth leakage current < 0.5 mA
Patient leakage current <
Patient auxiliary current D.C.
Patient auxiliary current A.C.
EN 60601-1-2 UL/CUL 60601-1, Class I, Type BF ordinary
EN 60601-1, Class I, Type BF, continuous operation
Power requirement
100 to 125 VAC nominal or 200 to 240 VAC nominal
50/60 Hz nominal 400 watts
<
0.1 Ω
< 0.1 mA
0.1 mA
<
0.01 mA
< 0.1 mA
Resolution
Paper Type Waveform Recording
Speeds
Programmer Reference Guide
Printer
600 dots/25 mm horizontally for waveform traces at print speeds through 25 mm/sec., 400 dots/25 mm at 50 mm/sec.; 200 dots/25 mm vertically
110 mm wide, Thermal, Medtronic No. 6092
12.5, 25 or 50 mm/s
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Tabl e 7 -1 . Programmer specifications
ECG specifications
Service the Programmer
Programmer specifications
89
Input Impedance at DC ECG Range of
Linear Operation ECG Total Signal Error Pacing Pulse Width
Physical dimension and weight
Height
Width Depth Weight
Operating Storage
Operating Storage
Data Interface
Analog Interface Data Modulation
>2.5 Me
- 5 mV to + 5 mV
< 10% > 100 µs to 2 ms
12.7 cm screen down, 48.2 cm screen up
40.6 cm
55.8 cm
11.3 kg including modem
Temperature limits
9.4 °C to 35 °C
- 22 °C to 60 °C
80% 95% at 35 °C
PCMCIA Release 2.1 compliant, 68-pin connector
RJ-11 modular telephone connector V.90/K56 flex up to 56 Kbps
Ω at 10 Hz
Humidity limits
Modem card
Data Interface
Data Modulation
Ethernet/modem card (Combo card)
PCMCIA Release 2.1 compliant, 68-pin connector
RJ-11 modular telephone connector RJ-45 Ethernet connector V.90/K56 flex up to 56 Kbps IEEE 802.3 10 Mbps full-duplex and
half-duplex on 10Base-T IEEE 802.3u 100 Mbps full-duplex and
half-duplex on 100Base-Tx
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Programmer specifications
Tab le 7 -1. Programmer specifications
On-board LAN (if present)
Data Interface Data Modulation
RJ-45 Ethernet connector IEEE 802.3 10 Mbps full-duplex and
half-duplex on 10Base-T IEEE 802.3u 100 Mbps full-duplex and
half-duplex on 100Base-Tx
Functional test, maintenance, and safety checks
Functional test at installation
Prior to putting the Programmer into service for the first time, the device and its accessories should be visually inspected and tested for operability by a designated Medtronic person. Visual inspection requires examining the Programmer case for cracks, verifying that all connectors are properly fastened, checking for insulation damage to the power cord and other accessory cables, and inspecting for wall plug and equipment plug damage.
Verify operation by turning on the Programmer and checking monitor functionality.
Maintenance
Medtronic recommends that the user should test the Programmer for operability and also visually inspect the Programmer and its accessories (e.g., power cord, cables) prior to each use as outlined in the section above.
Caution: If the case of the Programmer is cracked or if any of the connectors are damaged, contact your Medtronic or Vitatron representative. If there is insulation damage to the power cord or accessory cables or if any of the wall or equipment plugs are damaged, please replace the part and dispose of it according to local regulations or return the part to Medtronic.
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Safety checks
Safety checks require a functional test and electrical safety tests once every two years. It is not necessary that technical and safety inspections are performed by Medtronic or Vitatron personnel; however, technical and safety inspections of the Programmer and its accessories must be performed by persons, who, based on their training, knowledge, and practical experience, are capable of adequately performing such inspections and who do not require instructions with regard to the technical and safety inspection.
Warning: If technical and safety inspection reveals a defect which could harm the patient, clinicians, or third parties, the device should not be used until it has been properly repaired. The operator must immediately notify Medtronic or Vitatron of these defects.
Disposal of the Programmer
Return the Programmer to Medtronic or Vitatron for proper disposal.
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Special notice

91
Special notice
The Medtronic CareLink Model 2090 Programmer (the “Programmer”) is designed to program the adjustable parameters of the Medtronic or Vitatron programmable implantable devices included in the applications of the software used with the Programmer. Refer to the appropriate reference guides for a list of the implantable device models applicable to the software. The programming and telemetry functions of the Programmer are not compatible with any other implantable device models.
The Programmer also functions as a digital measuring device intended for measurement of the pulse rate, AV interval, and pulse width of implantable device artifacts as detected by skin electrodes. Medtronic and Vitatron make no claims or warranties as to the effectiveness of the Programmer as a diagnostic tool to the physician.
For information regarding difficulties, which may be encountered using the Programmer, consult other portions of this reference guide.
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Chapter 7

Medtronic limited warranty

Medtronic limited warranty
For complete warranty information, see the limited-warranty document enclosed in the package.
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Index

A
AC power cord 26 AC power input 26 ACMA 15 Adjust button 72 Adobe settings 62 AHA coding
electrodes 42
analog output
connections 24 artifact detection 79 Australia regulations 15 Auto Identify
see Find Patient
B
buttons
Adjust 72
Auto Identify
see Find Patient description 30 Emergency 49 Find Patient 30, 54 Freeze 72 I (programming head) 48 inactive 73 P (programming head) 48 Programmer 68
Emergency VVI 21 Vitatron/Medtronic switch 54
C
combo card 25
connecting Ethernet cable 35 connecting telephone line 35 replacing 87 specifications for 89, 90
components
storing 55, 56
concurrency 55
cooling fan 23
D
date and time
setting 73 Declaration of Conformity 15 demonstrations option 81 dimensions, programmer 89 disk drive 24 diskette, saving to 59 display screen
features of 27
E
ECG
cable 22, 23
cable connections 33
diagnostics 19
functions on the Programmer 19 electrocardiograms (ECG)
window, expanding 27 electrodes
AHA coding 42
attaching 42
IEC coding 42 Emergency button 21, 49, 50 environmental precautions
disposal of Programmer 9
while using Programmer 14 Ethernet cable 21 Ethernet/modem card
see combo card external components
see components external devices, connecting 37
F
features
Programmer 10 Federal Communications Commission (FCC) 15 Find Patient button 54 Find Patient screen 52 Freeze button 72
H
hardware information, programmer 81
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Index
I
I button (programming head) 48 icons
Analyzer indicator/selector 28 device indicator/selector 28 inactive 73 position head light array 28 Print Queue 72 Programmer 72 Select Model 72
IEC coding
electrodes 42 Industry Canada 15 input/output ports 26 interference 13
troubleshooting 37
L
live rhythm
window 27, 29 location, programmer 81 low paper supply 69
M
manual-guided reset 62 manuals
obtaining from website 84 Marker Channel telemetry 18, 37 model (device)
selection screen 54 model numbers 81 modem
replacing 87
specifications for 89 monitor, connecting 37
N
New Zealand regulations 15
O
ON/OFF switch 23, 36 operating preferences 74 operating temperature
programmer 89 other software
option 83
P
P button (programming head) 48 Paper Advance button 68 paper supply, low 69 patient session, conducting 51 PC card
see also combo card see also modem
replacing 87 PDF, saving to 58 pen
using 43 position head light 21 power cord
storing 26 precautions
environmental 14
Programmer 12
programmer modification 12 print queue settings 75 printer
access 23
buttons 68
compatibility 64
connecting 65
specifications 88 Printing
tearing off printout 69 profile, programmer 81 programmer
components 20
dimensions 89
functions 18
hardware information 81
location 81
preferences 74
profile 81
setting time and date 73
specifications 88
tool palette 72
view or update serial numbers 81
weight 89 programming head
buttons 48
determining the correct position 46
magnet 49
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Index
95
position head light 21 positioning 45, 47 sterilizing 86 when to position 46
Protected Health Information (PHI) 76
R
recorder, connecting 37 recovery of Vitatron devices 62 regulatory compliance 15 reports
deleting 75 saving session data 58 saving to diskette 59 saving to PDF 58 saving to USB 59 viewing 61
RTTE Directive
device conformance 15
S
screen
about the display 27 Find Patient 52
Select Model 54 selecting the device model 54 serial numbers 81 Skin Electrodes see electrodes software requirements 17 specifications
printer 88
programmer 88 standards, compliance 88 status bar 27, 29 storage temperature
programmer 89 system preferences 74
U
USB
saving to 59 storage devices 60
V
Vitatron device recovery 62 Vitatron/Medtronic switch button 54
W
warnings
programmer 11
warranty information
programmer 92
website
accessing technical manuals 84 weight, programmer 89 window
ECG 29
live rhythm 27, 29
T
task bar 28 telemetry
functions 18 Marker Channel 18, 37
temperature limits
programmer 89
time and date
setting 73
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Medtronic
Manufacturer
Medtronic, Inc. 710 Medtronic Parkway Minneapolis, MN 55432-5604 USA www.medtronic.com Tel. +1-763-514-4000 Fax +1-763-514-4879
Medtronic E.C. Authorized Representative/Distributed by
Medtronic B.V. Earl Bakkenstraat 10 6422 PJ Heerlen The Netherlands Tel. +31-45-566-8000 Fax +31-45-566-8668
Europe/Africa/Middle East Headquarters
Medtronic International Trading Sàrl Route du Molliau 31 Case Postale 84 CH-1131 Tolochenaz Switzerland www.medtronic.com Tel. +41-21-802-7000 Fax +41-21-802-7900
Vitatron
Distributed by
Vitatron Holding B.V. Endepolsdomein 5 6229 GW Maastricht The Netherlands Tel. +31-43-356-6551
Australia
Medtronic Australasia Pty Ltd 97 Waterloo Road North Ryde, NSW 2113 Australia
Technical manuals: www.medtronic.com/manuals
© Medtronic, Inc. 2011 M943414A001A 2011-04-05
*M943414A001*
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