Expression Model 865214 Instructions for Use Rev G Sept 2013

Manufacturer Invivo, a division of Philips Medical Systems 12151 Research Parkway Orlando, FL 32826 USA 877-468-4861 +31 (0) 499 378299 www.invivocorp.com

Copyright Copyright © 2013, Koninklijke Philips N.V. All rights reserved. REF 989803162691, Revision G, September 2013 Printed in USA

Proprietary Information This document and the information contained in it is proprietary and confidential information of Koninklijke Philips N.V. and may not be reproduced, copied in whole or in part, adapted, modified, disclosed to others, or disseminated without the prior written permission of the Koninklijke Philips N.V. This document is intended to be used by customers and is licensed to them as part of their Koninklijke Philips N.V. equipment purchase. Use of this document by unauthorized persons is strictly prohibited. Koninklijke Philips N.V. provides this document without warranty of any kind, implied or expressed, including, but not limited to, the implied warranties of merchantability and fitness for a particular purpose. Koninklijke Philips N.V. has taken care to ensure the accuracy of this document. However, Koninklijke Philips N.V. assumes no liability for errors or omissions and reserves the right to make changes without further notice to any products herein to improve reliability, function, or design. Koninklijke Philips N.V. may make improvements or changes in the products or programs described in this document at any time. New editions of this document will incorporate all material updated since the previous edition. Update packages may be issued between editions and contain replacement and additional pages to be merged by a revision date at the bottom of the page. Note that pages which are rearranged due to changes on a previous page are not considered revised. The documentation part number (REF) and revision indicate the current edition. The printing date changes when a new revision is printed. (Minor corrections and updates which are incorporated at reprint do not cause the date to change.) The document revision letter changes when extensive technical changes are incorporated.

ii

Contents Manufacturer... 1-ii Proprietary Information... 1-ii

Chapter 1: Important Information About This Manual... 1-1 Intended Audience... 1-1 Conventions... 1-2 System Conventions... 1-2 Document Conventions... 1-2 Warnings... 1-3 Cautions... 1-3 Notes... 1-3

Accessories... 1-3 CO2/Anesthetic Agents... 1-4 CO2 (Low Flow)/Anesthetic Agents... 1-4 CO2 (Standard Flow)/Anesthetic Agents... 1-4 ECG... 1-5 Gating Options... 1-5 Invasive Blood Pressure... 1-5 Mounting Options... 1-6 Non-invasive Blood Pressure (NIBP)... 1-6 Pneumatic Respiration... 1-7 Replacement Power... 1-7 SpO2... 1-8 Temperature... 1-9 Miscellaneous... 1-9

Safety... 1-10 Electromagnetic Compatibility (EMC)... 1-10 Radios... 1-10 Electromagnetic Emissions... 1-11 Electromagnetic Immunity... 1-12 Recommended Separation Distances of RF Communications Equipment... 1-14 Battery Disposal... 1-15 Disposing of Batteries in Europe... 1-15 Disposing of Batteries in the United States... 1-15 Used Accessory Disposal... 1-15

List of Symbols... 1-16 Installation... 1-21 Unpacking the System... 1-21 Packaging Disposal... 1-23

Equipment Classification... 1-24 Defibrillation... 1-24

System Installation... 1-25 Installing the Cart... 1-26 Installing the Display Control Unit... 1-29 Docking a DCU to the Cart... 1-29 Undocking a DCU from the Cart... 1-30 Using an Undocked DCU in the MR System Room... 1-31 Using a DCU in the MR Control Room... 1-33

Contents 1

Installing the Patient Management Configuration... 1-34 Additional Installation Options... 1-35

Chapter 2: System Overview Indications for Use... 2-1 System Parameters... 2-1 Device Configurations... 2-2 Warnings... 2-2

System Overview... 2-3 Cart Configuration... 2-4 Patient Management Configuration... 2-5 Display Control Unit... 2-7 DCU Alarm Light... 2-8 Patient Connection Area... 2-8 Wireless Modules... 2-9 WEGC Module... 2-9 wSpO2 Module... 2-9

Battery Operation... 2-11 Charging Batteries... 2-11 Using Batteries Safely... 2-12 Installing the Cart Batteries... 2-13 Removing the Cart Batteries... 2-13 Installing the PMC Batteries... 2-14 Removing the PMC Batteries... 2-16 Installing the DCU Batteries... 2-16 Removing the DCU Batteries... 2-16 Installing a Module Battery... 2-17 Removing a Module Battery... 2-17 Understanding the Module Status Indicator... 2-18 Changing the Module Network Setting... 2-18

Turning On the System... 2-22 Removing AC Mains Power... 2-22

User Interface... 2-22 DCU Power Switch... 2-23 DCU Status Indicator... 2-24 Speaker... 2-25 Keypad and Knob... 2-25 Displayed Groups... 2-28 Informational Group... 2-28 Vital Sign Box Group... 2-29 Vital Sign Trace Group... 2-31 System Status Group... 2-32

Chapter 3: Preparation for Use Monitor Initialization... 3-1 Setups Menu... 3-2 Setups Menu Options... 3-2 Recall Setups... 3-3

2 Contents

Store Setups... 3-3 Parameter Selection... 3-5 Sound Adjust... 3-6 Patient... 3-7 Pediatric ECG... 3-9 Set Time... 3-10 Default Setups... 3-11 Sweep Speed... 3-11 Resp Speed... 3-12 Network... 3-12 Service(Bio-Med)... 3-13

Chapter 4: Monitoring ECG Wireless ECG Module and Patient Lead Cables... 4-1 Attaching the Lead Cable to the Wireless Module... 4-2

Quadtrode Electrodes... 4-3 Electrode Selection... 4-3 Electrode Site Selection... 4-4 Prepping the ECG Patient Site and Placing the Quadtrode Electrode... 4-6 Checking the Electrode Contact Quality... 4-7 Connecting the Lead Cable to the Electrode and Positioning the wECG Module... 4-8 Positioning Suggestions... 4-9 Minimizing MRI-Related Heating Risks... 4-10

Monitor Setup... 4-11 ECG Filter Selection... 4-11 Checking the ECG Signal... 4-11

ECG Waveforms and VS Box... 4-13 ECG Menu Options... 4-14 Additional Functions... 4-20 Setting Alarm Limits... 4-20

ECG Gating... 4-20 Using Analog Gating... 4-20 Using Digital Gating... 4-21

ECG Messages... 4-22

Chapter 5: Monitoring SpO2 Wireless SpO2 Module, Sensor and Attachments... 5-1 SpO2 Patient Preparation... 5-2 Applying and Positioning the SpO2 Attachment on the Patient... 5-2 Positioning the wSpO2 Module for Scanning... 5-4 SpO2 Adult, Pediatric and Neonatal Operations... 5-5

SPO2 Waveform and VS Box... 5-6 SPO2 Menu Options... 5-7 Setting Alarm Limits... 5-8 Trended Data... 5-9

Assessing Suspicious SpO2 Readings... 5-9 SpO2 Messages... 5-10

Contents 3

Chapter 6: Monitoring Invasive Blood Pressure IBP Transducer Preparation... 6-1 IBP Waveforms and VS Boxes... 6-2 IBP Menu Options... 6-3 Additional Functions... 6-6 Setting Alarm Limits... 6-6

IBP Messages... 6-6

Chapter 7: Low Flow CO2 Option Water Trap and Sampling Line Preparation... 7-2 CO2 Warm-Up Period... 7-3 Using the Patient Airway Adaptor... 7-3 Water Trap Replacement... 7-4

Calibrating the CO2 Measurement System... 7-5 Zero Calibration Cycle... 7-5 Automatic Zero Cycle... 7-5

CO2 Waveform and VS Box... 7-6 CO2 Menu Options... 7-7 Additional Functions... 7-7 Setting Alarm Limits... 7-8

Low Flow CO2 Messages... 7-8

Chapter 8: Anesthetic Agents Option Operation and Use... 8-1 CO2 Warm-Up Period... 8-1 Zero Reference Adjustment... 8-2

Agents Tubing Preparation... 8-3 Pre-Use System Checks... 8-4 Water Trap Replacement... 8-5

CO2 Waveform and VS Box... 8-6 CO2 Menu Options... 8-8 Anesthetic Agents and Gas Vital Sign Activation... 8-8 Anesthetic Agents VS Box... 8-9 No Data Available Indication... 8-10 Multiple (Mixed) Agents... 8-10

Gas VS Box... 8-10 No Data Available Indication... 8-11

Setting Alarm Limits... 8-11 MAC Window... 8-12 MAC Calculation... 8-13

Low Flow and Occlusion Conditions... 8-14 Oxygen Sensor Depletion... 8-14 Anesthetic Agents Messages... 8-15

4 Contents

Chapter 9: Bellows Respiration Respiration Preparation... 9-1 Respiration Activation... 9-2 Respiration Box... 9-3

Chapter 10: Monitoring Temperature General Usage Precautions... 10-2 Sensor Use... 10-2 Initial Usage... 10-2 Connecting and Storing the Sensor... 10-2

Temperature Measurements... 10-3 Making Surface Temperature Measurements... 10-4 Making Body Temperature Measurements... 10-4 Placing the Sensor in a Jacket... 10-5

Post-Measurement Processing... 10-7 Cleaning and Disinfecting the Sensor... 10-7 Sterilizing... 10-9

Inspecting the Sensor for Damage... 10-9 Disposing of Used Jackets... 10-9 Temperature Display Indications... 10-9 Temperature Menu Options... 10-10 Additional Functions... 10-10 Setting Alarm Limits... 10-11

Temperature Messages... 10-11

Chapter 11: Monitoring Non-Invasive Blood Pressure Theory of Oscillometric Measurement... 11-2 NIBP Patient and Cuff Preparation... 11-3 Selecting the Cuff... 11-3 Positioning the Cuff... 11-3 Connecting the Cuff... 11-4

NIBP VS Box... 11-4 NIBP Systolic/Diastolic Display... 11-4 NIBP Mean Display... 11-6

NIBP Menu Options... 11-7 NIBP Adult, Pediatric and Neonatal Operations... 11-8 Additional Functions... 11-9 Setting Alarm Limits... 11-10 Controlling the Reading Cycle... 11-10 Auto Mode... 11-10 Manual Mode... 11-10

NIBP Messages... 11-11

Chapter 12: Printing, Trending, and Exporting Data Loading Paper... 12-1 Printing Charts... 12-3

Contents 5

Controlling Printer Outputs... 12-4

Printer Menu Options... 12-4 Trending Feature... 12-8 History Menu Options... 12-9 History File Page... 12-10 Multi Trends Menu... 12-11 Parameter Specific Trend Charts... 12-12 Clearing Trend Data... 12-12

Exporting Data... 12-12 Sending Data to External Systems... 12-15 Selectable Data Output Formatting... 12-15 Specifications... 12-15

Chapter 13: Managing Alarms Alarm Violations... 13-1 Alarm Limits... 13-2 Low and High Alarm Limits... 13-2 Default Alarm Limits... 13-3 Fixed Alarm Limits... 13-5

Controlling the Alarm Tone... 13-5 Alarms Menu Options... 13-7 Gas Alarms Options... 13-10

Controlling Individual Parameter Alarms... 13-11

Chapter 14: Maintenance and Repair Maintenance... 14-1 Cleaning... 14-1 Cleaning the Patient Monitoring System... 14-1 Cleaning Accessories... 14-2

Performing the CO2 Gas Verification Test... 14-3 Replacing the Oxygen Sensor... 14-4 Factory Default Initialization... 14-6 Service(Bio-Med) Menu Options... 14-7 Repair... 14-10

Appendix A: Specifications Specifications... A-1

Appendix B: Warranty Warranty... B-1

Appendix C: Regulatory Information European Union... C-1 Declaration of Conformity...C-1 Authorized Representative...C-1

6 Contents

Australia... C-1

Appendix D: Electromagnetic Compatibility Electromagnetic Compatibility (EMC)... D-1

Appendix E: Guidelines and References Guidelines for the Prevention of Excessive Heating and Burns Associated with Magnetic Resonance Procedures... E-1 References... E-3

Notes

Contents 7

8 Contents

Chapter 1 Important Information About This Manual Important user information about the Expression MRI Patient Monitoring System (Model 865214) and contact information for Invivo is discussed here. The terms “Cart” and “Patient Management Configuration” (PMC) are used throughout this manual to refer to the available configurations of the Expression MRI Patient Monitoring System. Specific differences between the configurations are noted where applicable. Information regarding the safety, accessories, installation, and operation of a fully equipped Expression MRI Patient Monitoring System (Model 865214) can be found in this document. Some information may depict monitoring features not present on your system. For information on all features and enhancements, contact Invivo or your Invivo sales representative: Invivo Orlando, FL 32826 877-468-4861 www.invivocorp.com For additional information about your accessories, please consult the documentation that accompanies the accessory. This product will perform in conformity with the description contained in this manual and accompanying labeling when assembled, operated, maintained, and repaired in accordance with the instructions provided. This device must be checked and calibrated periodically. A malfunctioning device must not be used. Parts that are broken, missing, plainly worn, distorted, or contaminated must be replaced immediately. Refer the device to qualified service personnel for repair or replacement. This device or any of its parts must not be repaired other than in accordance with written instructions provided by the manufacturer. The device shall not be altered without written approval of Invivo. The user has the sole responsibility for any malfunction which results from improper use, faulty maintenance, improper repair, damage or alteration by anyone other than authorized service personnel.

Intended Audience The Expression MRI Patient Monitoring System (Model 865214) is intended for use by healthcare professionals trained in the use of the equipment and vital signs monitoring.

Important Information

1-1

Conventions Certain conventions are used throughout the Expression MRI Patient Monitoring System (Model 865214) to speed use and familiarity with the device. This accompanying Instructions for Use also employs document conventions to assist you in finding and understanding information.

System Conventions These conventions are used when operating the Expression MRI Patient Monitoring System (Model 865214): •

The display panel includes a keypad and knob: – Press a key to activate or deactivate its function or to view its menu. – Turn the knob to navigate vital signs, parameters and menu options, or to increment or decrement fields, where the current item will be displayed in a highlighted field or background. – Press the knob to select a parameter, menu option or setting.

•

Most menus employ a time-out feature where, if no action is taken for approximately 60 seconds, an open menu will automatically close.

•

To protect against accidental changes, a YES/NO decision prompt is associated with certain menu options. When displayed, you must confirm or cancel this prompt; otherwise, a delay of approximately 30 seconds will be equivalent to selecting NO. (Note that the “NO” equivalent is also accomplished by pressing the NORMAL SCREEN key or the STANDBY key.)

•

To protect against unauthorized changes, some menu items feature password protection. You must enter the correct numeric code for access, where a delay of approximately 30 seconds is equivalent to making no entry.

Document Conventions These conventions are used in this document. •

All procedures are numbered, and all sub-procedures are lettered. Complete the steps in the sequence presented to ensure success. Procedures are indicated by the table below.

Step 1 2 3

1-2 Important Information

Action

•

During procedures, control names, menu items and titles are spelled and punctuated as they appear in the system.

•

The selection path to an option in the menu system is sometimes abbreviated with the greater than symbol (>) between menu items in the procedural string.

•

Bulleted lists indicate general information about a particular menu function or procedure, and do not imply sequential order or operation.

•

Where LCD images are presented, for clarity some of the black screen backgrounds have been replaced with a white background in this document for legibility.

•

The left side of the system is on your left as you stand in front of the system, facing it. The front of the system is nearest you as you operate it.

•

The front of the module is nearest you as you operate it.

Warnings WARNING Warnings provide information you should know to avoid injuring yourself, patients or personnel.

Cautions CAUTION Cautions provide information you should know to avoid damaging the equipment and software.

Notes NOTE Notes provide additional information you should know regarding system usage.

Accessories Accessories are listed in the tables below. Only use recommended Invivo accessories as other brands may compromise the safety and accuracy of the system.

Important Information

1-3

CO2/Anesthetic Agents Description

REF

CANNULA, DISP, ADULT

989803152561

CANNULA, DISP, ADULT,

989803152601

CANNULA, DISP, INT INF, (DIVIDED)

989803152621

CANNULA, DISP, PED, (DIVIDED)

989803152631

CANNULA, DISP, INFANT, (DIVIDED)

989803152611

CANNULA, DISP, INT INFANT

989803152591

CANNULA, DISP, PED

989803152571

ADPTR, ENDOTRACHEAL TUBE, 50 PK

989803152691

CAL GAS, AEROSOL CO-2

989803152641

KIT, WASTE GAS HOSE W/ADAPTER

989803152681

CO2 (Low Flow)/Anesthetic Agents Description

REF

KIT, WATER TRAP, ETCO2, 3160

989803152551

KIT, STARTER, ETCO2, 3160

989803152531

KIT, SAMPLE, ETCO2, 3160

989803152541

CO2 (Standard Flow)/Anesthetic Agents

1-4 Important Information

Description

REF

ANESTHETIC OXYGEN (O2) SENSOR

989803162051

ANESTHETIC OXYGEN (O2) SENSOR, INSTALLATION TOOL

989803162961

KIT, DISPOSABLE WATER TRAP

989803152671

KIT, STARTER, AGENTS, 3160

989803152651

KIT, SAMPLE, AGENTS

989803152661

ECG Description

REF

ADVANCED FILTER ECG CABLE

989803170121

KIT, STARTER, QUADTRODE CV, 3160

989803152261

CAB, 4 LD, CV MRI ECG

989803152351

KIT, STARTER, NEONATAL, MRI

989803152441

CAB, 4 LD, NEO.MRI ECG

989803152331

GEL, ECG/EEG, SKIN PREP, TUBE, 3-PACK

989803152291

KIT, STARTER, STANDARD ECG, 3160

989803152251

CAB, 4 LD, MRI ECG

989803152301

WIRELESS WECG MODULE

989803163121

QUADTRODE MRI ECG PAD, 25/BOX

989803179031

ELCTRD, MRI ECG, QUTRD.CV, 25/BOX

989803179041

ELCTRD, MRI,NEO.QUDTRD, 25/BOX

989803179051

Description

REF

CAB, DIGITAL GATING, GE, 3160

989803152821

CAB, DIG.GATING, HIT/TOSH, 3160

989803152851

CAB, GATING, SIEMENS, 3160

989803152831

CAB, GATING, PHILIPS ACH, 3160

989803152841

Gating Options

Invasive Blood Pressure Invivo recommends using the Edwards Lifesciences Transducer, Model PX260, and adapter cables. Please contact Edwards Lifesciences for an adapter cable that is compatible with Invivo devices. For additional questions, please contact your sales representative.

Important Information

1-5

Mounting Options Description

REF

WALL CHANNEL,POLYMOUNT,19"

989803152951

DOVETAIL CHAN,PIVOT ARM,OHMEDA

989803152961

WALL CHANNEL,PIVOT ARM,DRAEGER

989803152971

COLUMN, MOUNTING, DUAL CHANNEL, 8

453564215481

BRACKET, MOUNTING, NARCOMED,WPU

453564215491

KNOB,BAR,1/4-20 X 3/4 LG

453564240801

MRI MOUNTING ARM

989803162551

ASSEMBLY,WALL MOUNT,DCU

989803172451

NARKOMED STAINLESS STEEL HARDWARE KIT

989803172811

Non-Invasive Blood Pressure (NIBP)

1-6 Important Information

Description

REF

KIT, STARTER, NEONATAL, MRI

989803152441

HOSE, NEO, 15 FT, MRI

989803169421

HOSE, ADULT, 18’, MRI

989803169411

KIT, ACCESSORIES, NIBP, MRI

989803152451

CUFF, NIBP, DISP, SAMPLE KIT

989803170501

CUFF, INFANT, MRI, COLDER CONN

989803169431

CUFF, CHILD, MRI, COLDER CONN

989803169441

CUFF, ADULT, MRI, COLDER CONN

989803169451

CUFF, LARGE ADULT, MRI, COLDER CONN

989803169461

CUFF, DISP, NEO, MRI SIZE#3

989803170401

CUFF, DISP, NEO, MRI SIZE#5

989803170421

CUFF, NIBP, DISP, INFANT, 10 - 15CM

989803170431

CUFF, NIBP, DISP, PEDIATRIC, 14 - 21CM

989803170441

CUFF, NIBP, DISP, SMALLADULT, 20 - 28CM

989803170451

CUFF, NIBP, DISP, ADULT, 27 - 36CM

989803170461

NIBP (continued) Description

REF

CUFF, NIBP, DISP, ADULT EXTRA-LONG, 27 - 36CM

989803170471

CUFF, NIBP, DISP, LARGE ADULT, 35 - 45CM

989803170481

CUFF, NIBP, DISP, LARGE ADULT EXTRA-LONG, 35-45CM

989803170491

Description

REF

PNEUMOGRAPH, CHEST, NM, 3160

989803152791

Pneumatic Respiration

Replacement Power Description

REF

BATTERY, MRI, 14.8V, 5.08 AH, UL

989803169491

CAB, POWER, ADAPTER, 25FT, 3155

989803152231

CAB,POWER,ADAPTER,5FT,3155 SER

989803152221

NORTH AMERICAN LINE CORD

989803168211

EUROPEAN LINE CORD

453564177501

UK LINE CORD, 3 METER

989803174171

BRAZILIAN POWER CORD, 3 METER

989803173901

ASSEMBLY, POWER CORD SET 220V

989803152191

MR COMPATIBLE POWER CONVERTER

989803168201

BATT.3.7V, WRLS. PAT. MDLE.

989803152881

ASSY, 3.7V BATTERY CHARGER, 3160

989803152891

DCU POWER CONVERTER KIT

453564123631

KIT,POWER CONVERTER,MRFUSION

989803171721

ASSY,LINE CORD,110 V,TESTED

989803152181

POWER CORD, AUS/NZL, 3 METER

989803181291

POWER CORD, S AFRICA, 3 METER

989803181321

Important Information

1-7

Replacement Power (continued) Description

REF

POWER CORD, DANISH, 3 METER

989803181331

POWER CORD, ISRAELI, 3 METER

989803181341

POWER CORD, ARGENTINA, 3 METER

989803181351

POWER CORD, SWISS, 3 METER

989803181361

Description

REF

QUICK CONNECT SPO2 CLIP, ADULT

989803166531

QUICK CONNECT SPO2 CLIP, PEDIATRIC

989803166541

QUICK CONNECT SPO2 GRIP, ADULT, 20/BOX

989803166551

QUICK CONNECT SPO2 GRIP, PED, 20/BOX

989803166561

QUICK CONNECT SPO2 GRIP, INFANT, 20/BOX

989803166571

QUICK CONNECT SPO2 GRIP, NEO, 20/BOX

989803166581

QUICK CONNECT SPO2 STARTER KIT

989803167111

QUICK CONNECT SPO2 PROBE, MRI

989803161991

SPO2 SENSOR GRIP ADULT/NEONATAL 2 PACK

989803162501

SPO2 SENSOR GRIP INFANT/PEDIATRIC 2 PACK

989803162511

WIRELESS SP02 MODULE (GEN 2)

989803163111

GRIP SENSOR STARTER KIT

989803162491

SpO2

1-8 Important Information

Temperature Description

REF

FLEXTEMP SYSTEM, SENSOR

989803178171

SURGICAL LUBRICANT, 12 PACK

989803168891

FLEXTEMP SYSTEM, JACKET

989803178181

APPLICATOR,TEMP.SNSR,F.O.

989803152811

Description

REF

2.4 GHZ, ANTENNA

453564125581

ADVANCED COMMUNICATIONS OPTION

989803176521

CONTROL ROOM FLEX ANTENNA

989803176511

HOLDER, ACCESSORIES, CART

453564145951

PAPER,THERM ARRAY PRNTR (10PK)

989803152911

3160P OPERATORS MANUAL

989803162691

MANUAL, OPERATIONS, 3160P, DANISH

989803169211

MANUAL, OPERATIONS, 3160P, DUTCH

989803169221

MANUAL, OPERATIONS, 3160P, FRENCH

989803169231

MANUAL, OPERATIONS, 3160P, GERMAN

989803169241

MANUAL, OPERATIONS, 3160P, ITALIAN

989803169251

MANUAL, OPERATIONS, 3160P, NORWEGIAN

989803169261

MANUAL, OPERATIONS, 3160P, BRAZILIAN POR

989803169271

MANUAL, OPERATIONS, 3160P, SPANISH

989803169291

MANUAL, OPERATIONS, 3160P, SWEDISH

989803169301

MANUAL, OPERATIONS, 3160P, RUSSIAN

989803170271

MANUAL, OPERATIONS, 3160P, POLISH

989803173101

MANUAL, OPERATIONS, 3160P, JAPANESE

989803173171

Miscellaneous

Important Information

1-9

Miscellaneous (continued) Description

REF

MANUAL, OPERATIONS, 3160P, SIMPLIFIED CH

989803173181

MANUAL, OPERATIONS, 3160P, TRADITIONAL C

989803173191

MANUAL, OPERATOR, EXPRESSION, FINNISH

989803179331

MANUAL, OPERATIONS, EXPRESSION, CZECH

989803179351

QUICK REFERENCE GUIDE, ENGLISH

989803162711

3160P SERVICE MANUAL

989803162701

EXPRESSION PLUS

989803180471

FILTER,13MM,1.0UM HYDRO.,M/F

453564181961

Safety Electromagnetic Compatibility (EMC) The device is intended for use in the electromagnetic environment specified below. Given the device’s electromagnetic emissions and immunity characteristics, the customer or user should assure that the device is used within such an environment.

Radios Radio Frequency (RF) Range: 2402 to 2482 MHz Modulation Type: GMSK WPU EIRP: 4.2 dBm (peak) wECG and WSPO2 EIRP: 0 dBm (peak)

1-10 Important Information