Invivo
Expression Model 865214 Instructions for Use Rev G Sept 2013
Instructions for Use
269 Pages
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Page 1
MRI Patient Monitoring System (Model 865214) INSTRUCTIONS FOR USE Revision G English
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