CARESCAPE Canvas 1000 and Canvas Smart Display Supplemental Information Manual sw ver 3 (3.3) 1st Edition

Supplemental Information Manual

Contents

Contents Introduction to this manual ... 11 Intended use of this manual ... 11 Intended markets of this manual...12 Intended audience of this manual ...12 About these devices... 12 Safety precautions... 12 Manual conventions ... 12 Monitor naming conventions ...12 Acquisition module naming conventions ...13 Other naming conventions ... 13 Related documents... 14 Ordering manuals... 15 Revision history... 15 Accessing manuals online ... 15 Product availability ... 15

Compliance... 17 Standards compliance... 17 IEC 60601-1... 17 Compliant devices... 17

Design, environmental, and physical specifications ... 19 Design, environmental, and physical specifications...19 CARESCAPE Canvas 1000 specifications...19 CARESCAPE Canvas Smart Display specifications ...20 CARESCAPE Canvas D19 display specifications ...21 F2 Frame specifications... 22 F5 Frame specifications... 22 F7 Frame specifications... 23 CARESCAPE Patient Data Module specifications...23 PDM battery specifications... 23 CARESCAPE respiratory module specifications...24 E-miniC module specifications...24 E-PP and E-PT module specifications...24 E-COP and E-COPSv module specifications ...25 E-PiCCO module specifications...25 E-EEGX module and N-EEGX headbox specifications ...25 E-ENTROPY module specifications...25 E-NMT module specifications ...26 E-BIS module specifications ... 26 E-MASIMO module specifications...26 5697480-02

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E-NSATX module specifications...26 E-musb module specifications ...27 B1X5-REC recorder specifications ...27 USB remote control specifications ...27

Alarm specifications... 29 About alarms ... 29 Alarm standards compliance ... 29 Auditory alarm volume, IEC tones...29 Auditory alarm volume, legacy tones ...30 Audio alarm sound tolerances... 31 Legacy alarm tone sound patterns...31 IEC alarm tone sound patterns ...32 Remote alarm tone sound patterns...32 Auditory information signal characteristics ...32 Visual information signals ... 33 Alarm delay specifications... 33 Time to alarm for tachycardia...33 Physiological alarm delay specifications...34 Alarm delay specifications for ECG alarms...34 Alarm delay specifications for impedance respiration alarms...36 Alarm delay specifications for SpO2 alarms...36 Alarm delay specifications for rSO2 alarms...37 Alarm delay specifications for NIBP alarms ...38 Alarm delay specifications for invasive pressures alarms ...38 Alarm delay specifications for temperature alarms ...42 Alarm delay specifications for cardiac output alarms ...43 Alarm delay specifications for SvO2 and ScvO2 alarms ...43 Alarm delay specifications for airway gases alarms...43 Alarm delay specifications for spirometry and gas exchange alarms...45 Alarm delay specifications for Entropy alarms ...46 Alarm delay specifications for NMT alarms...46 Alarm delay specifications for BIS alarms...46 Technical alarm delay specifications ...46 Remote alarm delay specifications ...57 Alarm priorities and escalation times ...57 Alarm priorities and escalation times for ECG ...57 Alarm priorities and escalation times for impedance respiration...64 Alarm priorities and escalation times for SpO2 ...65 Alarm priorities and escalation times for rSO2 ...69 Alarm priorities and escalation times for NIBP...70 Alarm priorities and escalation times for invasive pressures...72 Alarm priorities and escalation times for temperature ...80 Alarm priorities and escalation times for cardiac output...81 Alarm priorities and escalation times for CCO...82 4/282

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Contents

Alarm priorities and escalation times for SvO2 and ScvO2...83 Alarm priorities and escalation times for airway gases...85 Alarm priorities and escalation times for spirometry...91 Alarm priorities and escalation times for gas exchange...92 Alarm priorities and escalation times for Entropy...93 Alarm priorities and escalation times for NMT ...94 Alarm priorities and escalation times for EEG and AEP...95 Alarm priorities and escalation times for BIS ...96 Alarm priorities and escalation times for TC...97 Alarm priorities and escalation times for trends, snapshots, and laboratory data ...97 Alarm priorities and escalation times for various situations...98

Parameter specifications... 105 Parameter specifications ... 105 About parameters... 105 ECG standards compliance... 105 ECG performance specifications ... 105 Impedance respiration performance specifications ... 108 SpO2 standards compliance... 109 SpO2 displayed saturation values... 109 SpO₂ summary of clinical studies used to establish accuracy claims... 109 Accuracy of Nellcor Oximax technology with Oximax sensors... 109 Accuracy of SpO2 with the MAX-N sensor ... 110 Accuracy of SpO2 with Softcare SC-PR and SC-NEO sensors ... 110 Accuracy of Masimo SET technology with Masimo SET sensors ... 110 SpO2 test methods used to establish accuracy claims during motion... 110 SpO₂ test methods used to establish accuracy claims during low perfusion... 111 Low perfusion accuracy of Nellcor Oximax technology with Oximax sensors ... 111 Low perfusion accuracy of Masimo SET technology... 111 SpO₂ test methods used to establish pulse rate accuracy ... 111 Pulse rate accuracy of Nellcor Oximax technology with Oximax sensors ... 111 Pulse rate accuracy of Masimo SET technology with Masimo sensors... 112 SpO2 performance specifications ... 112 SpHb performance specifications... 115 rSO2 performance specifications ... 116 NIBP standards compliance... 116 NIBP performance specifications... 116 Invasive pressure standards compliance... 117 Invasive pressure performance specifications... 117 SPV and PPV calculations... 118 Temperature standards compliance... 118 Temperature performance specifications ... 118 C.O. standards compliance ... 119 Cardiac output (C.O.) performance specifications... 120 CCO performance specifications... 121 E-PiCCO calculation formulas... 122 SvO2 and ScvO2 performance specifications... 123 5697480-02

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Supplemental Information Manual

Airway gases standards compliance ... 124 Airway gases normal conditions ... 124 Airway gases performance specifications... 124 Airway gases calculations ... 129 Airway gases CO2 unit conversions ... 130 Spirometry normal conditions... 130 Spirometry performance specifications... 131 Spirometry calculations... 132 Spirometry airway pressures calculations... 132 Spirometry airway flow calculations ... 132 Spirometry compliance calculations ... 132 Spirometry airway resistance calculations... 132 Gas exchange performance specifications ... 132 Gas exchange calculation formulas ... 133 Entropy standards compliance ... 134 Entropy performance specifications... 134 Entropy calculations ... 135 NMT standards compliance ... 135 NMT performance specifications ... 135 EEG standards compliance ... 136 EEG performance specifications... 136 BIS standards compliance ... 137 BIS performance specifications ... 137 BIS calculations ... 138

Calculation specifications ... 139 About calculations and drug calculations... 139 Drug calculation specifications ... 139 Drug calculation formulas ... 139 Resuscitation medications calculations... 140 Laboratory data calculations... 140 Hemodynamic calculation specifications ... 141 Hemodynamic calculations input parameter specifications ... 141 Hemodynamic calculations calculated parameter specifications... 141 Hemodynamic calculations calculated parameter formulas... 142 Oxygenation calculation specifications ... 143 Oxygenation calculations input parameter specifications ... 143 Oxygenation calculations calculated parameter specifications... 144 Oxygenation calculations calculated parameter formulas... 144 Ventilation calculation specifications... 146 Ventilation calculation input parameter specifications ... 146 Ventilation calculations calculated parameter specifications ... 146 Ventilation calculations calculated parameter formulas ... 146

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Contents

Understanding your monitor configuration ... 149 Software packages ... 149 Software features ... 149 Licensed software options... 149 Software profiles ... 150 Software settings ... 151 Care unit settings... 151 DEMO MODE... 151 Exiting the DEMO MODE ... 152 Profile settings... 152 Current patient settings... 152 Configuring care unit settings... 152 Alarm settings... 153 Parameter alarms settings ... 155 Screen settings... 157 Admit/discharge settings... 157 Unit of measure settings... 158 Parameter/demographics unit of measure settings... 158 Laboratory values unit of measure settings ... 159 Calculations unit of measure settings ... 160 Parameter settings... 160 12 lead ECG settings... 161 ECG settings ... 162 Temperature label settings... 162 Catheter settings ... 162 Drug list settings... 163 ED, ICU, OR and PACU software package drug list default settings... 163 NICU software package drug list default settings ... 163 Standby site name settings ... 164 Show in Screen Setup settings... 164 Roving settings ... 165 Telemetry settings ... 165 Print settings... 165 Configuring profile settings... 165 Absolute alarm limit settings... 166 Alarm delay settings ... 170 V Tach Event Duration Criteria... 170 Invasive pressures alarms settings ... 170 Invasive pressures colors settings for labels... 175 Page settings... 175 Upper parameter area settings ... 176 Lower parameter area settings ... 187 Primary screen split screen settings ... 190 Secondary screen split screen settings... 191 Trends and snapshot settings... 191 General trend settings... 191 Graphic trends page settings... 191 5697480-02

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Snapshot settings ... 195 Care report settings ... 196 Configuring locking settings... 197 General locking settings... 198 Parameter locking settings ... 198 Alarm locking settings... 198 Configuring Time & Date settings ... 202 Time Format settings ... 202 Configuring current patient settings... 202 Alarm limits settings... 202 Alarm priority settings ... 202 Arrhythmia alarm settings... 204 Lethal alarm settings... 204 V Tach Criteria settings ... 205 Ventricular alarm settings... 205 Atrial alarm settings ... 207 Audible and visual alarm settings... 208 Monitor screen settings... 209 Monitor brightness settings ... 209 Invasive pressures color settings for channels ... 209 Other parameters color settings... 209 Monitor sound settings... 210 Monitor parameter settings ... 211 Waveform printout settings... 211 Report settings... 211 Device settings ... 212 Drug calculator settings ... 213 Calculator default settings ... 213 Titration table default settings ... 213 Resuscitation medication settings... 213 Laboratory data settings... 214 Calculation settings... 214 Other patients (remote alarm) settings ... 214 Admit/discharge or start/end case settings... 215 Trend settings ... 216 Trend scales default settings ... 218 Parameter default settings ... 221 ECG default settings ... 221 ECG setup default settings ... 221 ECG advanced default settings... 223 ECG arrhythmia alarm default settings ... 226 ST default settings ... 226 ST alarms default settings... 227 QT default settings ... 228 QT setup default settings ... 228 QT alarms default settings... 228 QTc alarms default settings... 229 8/282

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Supplemental Information Manual

Contents

Impedance respiration default settings ... 229 SpO2 default settings ... 230 SpHb default settings... 233 rSO2 default settings ... 233 NIBP default settings ... 234 Invasive pressures default settings... 236 Art 1 pressure site default settings... 236 UAC 1 pressure site default settings ... 237 CVP 2 pressure site default settings... 238 UVC 2 pressure site default settings ... 239 Fem 3 pressure site default settings ... 240 Art 3 pressure site default settings... 241 PA 4 pressure site default settings... 242 CVP 4 pressure site default settings... 243 P5 to P7 pressure site default settings... 243 Art 8 pressure site default settings... 244 Temperature default settings ... 246 T1, T2 default settings... 246 T3, T4 default settings... 246 Tblood default settings... 247 Cardiac output (C.O.) default settings... 248 CCO default settings... 249 SvO2 and ScvO2 default settings... 250 Airway gases default settings... 250 CO2 default settings ... 250 O2 default settings ... 252 Anesthetic agent default settings ... 252 Spirometry and gas exchange default settings... 254 Entropy default settings... 255 NMT default settings... 256 EEG default settings... 257 EEG montage default settings... 258 AEP default settings... 259 BIS default settings... 260 Transcutaneous CO2/O2 default settings ... 260

Maintenance... 261 Before any planned maintenance or regular checks ... 261 Planned maintenance for the monitor and secondary display ... 261 Planned maintenance for the modules ... 261 Planned maintenance for the frames... 261 Regular checks... 262 Daily checks ... 262 Check every two months ... 262 Check every six months... 262 Check every 12 months... 262 Check every 24 months... 262 5697480-02

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Supplies and accessories ... 263 About supplies and accessories... 263 Ordering information ... 263

SpO₂ supplemental analysis graphs... 265 Additional accuracy information for Nellcor sensors with E-NSATX and PDM (Nellcor) ... 265 Additional accuracy information for Masimo sensors ... 265

Electromagnetic compatibility ... 271 IEC 60601-1-2 ... 271 Electromagnetic compatibility safety precautions... 271 Essential performance in EMC... 272 EEG accessories and electromagnetic compatibility... 273 BIS accessories and electromagnetic compatibility ... 274 Electromagnetic emissions... 274 Electromagnetic immunity... 275 Electromagnetic immunity for RF ... 276 Recommended separation distances... 277 Proximity field immunity compliance... 278

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Introduction to this manual Intended use of this manual The information in this manual applies to the software version listed on the first page of the manual. This manual must be used in conjunction with the user manual for important safety information and detailed instructions for clinical use of these products. Devices and versions not specifically stated are not supported and should not be used with the monitor. The list below indicates the compatible products (brands, models and descriptions as applicable) with which this manual is to be used. Supported products are covered by the manuals that were delivered with those products. • CARESCAPE Canvas™ 1000 • CARESCAPE Canvas™ Smart Display • CARESCAPE™ Software version 3 (3.3) • CARESCAPE Canvas™ D19 • E-COP-01, E-COPSv-01 • E-PiCCO-00 • E-sCAiO-00, E-sCAiOV-00, E-sCAiOVX-00, E-sCO-00, E-sCOV-00, E-sCOVX-00, E-sCAiOE-00, EsCAiOVE-00 • E-miniC-00 • E-MASIMO-00 • E-NSATX-00 • E-PP-00, E-PT-00 • E-ENTROPY-01 • E-NMT-01 • E-EEGX version MJD101, N-EEGX version MJS101 • E-BIS-01 • E-musb, version MJU101 • CARESCAPE™ Patient Data Module, CARESCAPE™ Patient Data Module GS • B1X5-REC recorder • Frame F5–01, Frame F7–01 • F2-01 • USB Remote Control • CARESCAPE™ RAD, Remote Alarm Device, version MBRA001

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Intended audience of this manual

Supplemental Information Manual

Intended markets of this manual This manual is not intended for other than U.S. FDA-regulated markets because supplies and accessories, features, and defaults in those countries differ from those cleared for use by the U.S. FDA.

Intended audience of this manual This manual is intended for clinical professionals. Clinical professionals are expected to have a working knowledge of medical procedures, practices and terminology required to provide patient care. Using the system should never replace nor impede the human intervention and required patient care provided by clinical professionals. This manual is also intended for service representatives and technical personnel who install, maintain, troubleshoot, or repair this device.

About these devices Refer to the user manual for important information about the monitor, including intended use of the device, important safety information and detailed instructions for clinical use of the product.

Safety precautions Refer to the user manual for important system safety messages. Safety messages specific to parts of the system are found in the relevant section. Read all the safety information before using the monitor for the first time.

Manual conventions This manual uses the following styles to emphasize text or indicate an action. Also note the terminology conventions. Item

Description

Courier

Indicates hardware keys and connectors.

bold

Indicates software terms.

italic

Indicates terms for emphasis.

>

Indicates menu options to select consecutively.

select

The word select means choosing and confirming.

acquisition device

A generic term when referring to both the acquisition modules (PDM, E-modules) and the acquisition platform (CARESCAPE ONE).

NOTE

Note statements provide application tips or other useful information.

Monitor naming conventions In this manual, the CARESCAPE Canvas 1000 and CARESCAPE Canvas Smart Display are referred to as the monitor when a function or a feature applies to both. For describing monitor-specific issues, the monitors are referred to as Canvas 1000 and Canvas Smart, respectively.

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Manual conventions

Acquisition module naming conventions In this manual, the following naming conventions are used to refer to different modules and module categories: • PDM: CARESCAPE Patient Data Module • E-modules: All modules with the prefix E-. • E-COP, E-COPSv • E-PiCCO • Pressure E-modules: E-PP, E-PT • CARESCAPE respiratory modules: E-sCO, E-sCOV, E-sCOVX, E-sCAiO, E-sCAiOV, E-sCAiOVX, EsCAiOE, E-sCAiOVE • E-miniC • Specialty E-modules: E-NMT, E-EEGX, E-BIS, E-ENTROPY • SpO2 E-modules: E-NSATX, E-MASIMO • E-musb: CARESCAPE Parameter interface module

Other naming conventions For technical documentation purposes, the abbreviation GE is used for the legal entity names, GE Medical Systems Information Technologies, Inc., and GE Healthcare Finland Oy. In this manual, CARESCAPE Network is used to refer to both the IX Network and MC Network except where they need to be differentiated. Then they are referred to as IX Network and MC Network. In this manual, the CARESCAPE ONE acquisition platform may also be referred to as CS ONE. In this manual the CARESCAPE Canvas D19 is referred to as the D19 display or secondary display. In this manual, the following naming conventions are used to refer to different frames: • F7 Frame: Frame F7-01 • F5 Frame: Frame F5-01 • F2 Frame: F2-01 In this manual the B1X5-REC recorder is referred to as the local recorder. In this manual, CARESCAPE Parameters is used as a generic term when referring to all of the following products: Graphic on the CARESCAPE Pa- Explanation rameter CARESCAPE Parameter for measuring ECG. Note that in the manual, the following name is used instead of the graphic: CARESCAPE ECG. CARESCAPE Parameter for measuring invasive pressures. Note that in the manual, the following name is used instead of the graphic: CARESCAPE Pressure. CARESCAPE Parameter for measuring regional oxygen saturation of blood (rSO2) in cerebral and somatic tissues with INVOS technology. Note that in the manual, the following name is used instead of the graphic: CARESCAPE rSO2.

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Related documents

Supplemental Information Manual

Graphic on the CARESCAPE Pa- Explanation rameter CARESCAPE Parameter for measuring temperature. Note that in the manual, the following name is used instead of the graphic: CARESCAPE Temperature. CARESCAPE Parameter for measuring CO2 with Respironics LoFlo technology. Note that in the manual, the following name is used instead of the graphic: CARESCAPE CO2 - LoFlo. CARESCAPE Parameter for measuring end-tidal carbon dioxide (EtCO2), FiCO2, and respiration rate with Microstream technology. Note that in the manual, the following name is used instead of the graphic: CARESCAPE CO2 - Microstream. CARESCAPE Parameter for measuring SpO2 with GE TruSignal technology. Note that in the manual, the following name is used instead of the graphic: CARESCAPE SpO2. CARESCAPE Parameter for measuring SpO2 with Masimo rainbow SET technology. Note that in the manual, the following name is used instead of the graphic: CARESCAPE SpO2 - Masimo. CARESCAPE Parameter for measuring SpO2 with Nellcor™ sensors with OxiMax™ technology. Note that in the manual, the following name is used instead of the graphic: CARESCAPE SpO2 - Nellcor.

In this manual, CARESCAPE CO2 is used as a generic term when referring to all of the following products: CARESCAPE CO2 - LoFlo and CARESCAPE CO2 - Microstream. In this manual, CARESCAPE SpO2 device is used as a generic term when referring to all of the following products: CARESCAPE SpO2, CARESCAPE SpO2 - Nellcor, and CARESCAPE SpO2 - Masimo. In this manual, acquisition platform refers to the CARESCAPE ONE. In this manual, the following product names are used as generic terms: • D-lite when referring to D-lite, D-lite+, and D-lite++ • Pedi-lite when referring Pedi-lite and Pedi-lite+ • D-fend Pro when referring to D-fend Pro and D-fend Pro+ • D-lite(+) when referring to D-lite and D-lite+. Does not apply to D-lite++.

Related documents • CARESCAPE Canvas 1000 and CARESCAPE Canvas Smart Display User Manual • CARESCAPE Canvas 1000 and CARESCAPE Canvas Smart Display Supplies and Accessories Supplement • Cleaning and Disinfection Supplement • Monitor Software Compatibility Supplement for CARESCAPE Software Version 3 (3.3) • Marquette 12SL ECG Analysis Program Physician’s Guide • CARESCAPE ONE User Manual • Instructions for use for CARESCAPE rSO2 - INVOS • Instructions for use for CARESCAPE CO2 - Microstream • Instructions for use for B1X5-REC recorder 14/282

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Ordering manuals

• CARESCAPE Modular Monitors Mounting Solutions • CARESCAPE Central Station User’s Manual • Unity Network Interface Device (ID) User's Manual • CARESCAPE Canvas 1000 and CARESCAPE Canvas Smart Display Service Manual • CARESCAPE Canvas D19 Service Manual • Service manuals for acquisition modules and module frames • CARESCAPE Network Configuration Guide • CARESCAPE Canvas 1000 and CARESCAPE Canvas Smart Display Privacy and Security Manual. Security related documents can be downloaded from https://securityupdate.gehealthcare.com. For a list of third-party or open-source software included in the device, please contact your GE service representative.

Ordering manuals A paper copy of this manual will be provided upon request. Contact your local GE representative and request the part number on the first page of the manual.

Revision history Revision

Description

1st edition

Initial release.

Accessing manuals online To obtain the latest version of the manual: 1.

Go to https://www.gehealthcare.com/documentationlibrary.

2.

Enter the Customer Documentation Portal.

3.

Select Modality > Monitoring Solutions (MS).

4.

Select Products > the products you want to search. You may also select the Document Type and Language to narrow down the search.

5.

Launch the search.

6.

Identify and download the manual.

The manuals are in PDF format. Make sure that your viewing device (for instance, computer) has software to open the PDF files (for instance, Adobe® Acrobat® Reader). Security related documents can be downloaded from https://securityupdate.gehealthcare.com.

Product availability NOTE Due to continual product innovation, design and specifications for these products are subject to change without notice. 5697480-02

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Product availability

Supplemental Information Manual

Some of the products mentioned in this manual may not be available in all countries. Please consult your local representative for the availability.

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Compliance Standards compliance The system complies with the following standards. • IEC 60601-1:2020-08 • IEC 60601-1-2:2020-09 • IEC 60601-1-6:2020-07 • IEC 62366-1:2020-06 Compliance to parameter and function specific standards is disclosed in the applicable sections. Compliance applies only to those products that are currently being manufactured and shipped. It does not apply to older devices or devices that have had their software upgraded.

IEC 60601-1 • Type of protection against electrical shock: Class I. • Degree of protection against electrical shock: applied parts are marked with a symbol indicating degree of protection. • Degree of safety of application in the presence of flammable anesthetic mixture with air or with oxygen or nitrous oxide: Not suitable. WARNING EXPLOSION. Do not use this equipment in the presence of flammable anesthetics, vapors or liquids. • Degree of protection against harmful ingress of water: IPX1 (minimum), see individual device specifications. • Mode of operation: Continuous. • Method(s) of sterilization or disinfection recommended by the manufacturer: see the supplemental information provided.

Compliant devices The devices listed in the following table have been verified to be compliant with the standard 60601-1:2020, 3.2 edition: Monitor

CARESCAPE Canvas 1000 and CARESCAPE Canvas Smart Display

Secondary display

CARESCAPE Canvas D19

Acquisition platform

CARESCAPE ONE with software version 3.2

PDM

CARESCAPE Patient Data Module (product code SPX) software v2.9 (Masimo and Nellcor)

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Compliant devices

E-modules

Supplemental Information Manual

E-BIS-01

E-NSATX-00

E-COP-01

E-PP-00

E-COPSv-01

E-PT-00

E-PiCCO-00

E-sCAiO-00 (product code SUA)

E-EEGX MJD101, N-EEGX MJS101

E-sCAiOE-00 (product code SUA)

E-ENTROPY-01

E-sCAiOV-00 (product code SUA)

E-MASIMO-00

E-sCAiOVX-00 (product code SUA)

E-miniC-00 (product code SUB)

E-sCAiOVE-00 (product code SUA)

E-musb MJU101, with:

E-sCO-00 (product code SUA)

• CARESCAPE rSO2

E-sCOV-00 (product code SUA)

• CARESCAPE CO2 - Microstream

E-sCOVX-00 (product code SUA)

E-NMT-01 Frames

F0 docking station Frame F5-01 and Frame F7-01 F2-01

Peripherals

B1X5-REC recorder CARESCAPE RAD, version MBRA001 2093421–001 USB Barcode Reader and Mount 2077698–001 USB Mouse 2077699–0xx USB Washable Keyboards 2039040-0xx USB Remote Unity Network ID v10B

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Design, environmental, and physical specifications Design, environmental, and physical specifications For CARESCAPE ONE and F0 docking station specifications, refer to the CARESCAPE ONE manuals. For additional specifications, refer to the documentation provided with your equipment. For more information on modules that can be used with the system, refer to the Monitor Software Compatibility Supplement. Operating altitude: The system shall meet specifications when subjected to altitudes corresponding to pressure readings from 700 mbar to 1060 mbar. NOTE An average pressure reading of 700 mbar corresponds to an altitude of 3000 m (10,000 ft) and 1060 mbar corresponds to an altitude of –400 m (–1000 ft). Non-operating altitude: The system shall meet specifications after being subjected to altitudes corresponding to pressure readings from 500 mbar to 1060 mbar. NOTE An average pressure reading of 500 mbar corresponds to an altitude of 5486 m (18,000 ft).

CARESCAPE Canvas 1000 specifications WARNING INACCURATE RESULTS. Do not use or store the equipment outside the specified temperature, humidity, or altitude ranges, or outside the specified performance range. Using or storing the equipment outside the specified operating environment or outside the specified performance range may cause inaccurate results. Size (H x W x D)

388 × 440 × 126 mm

Weight

7.6 kg (16.6 lb)

Operating temperature range

10 to 40°C (50 to 104°F)

Non-operating temperature range

-20 to 60°C (-4 to 140°F)

Operating humidity range

15 to 90% RH non-condensing

Non-operating humidity range

10 to 90% RH non-condensing

Operating altitude range

700 mbar to 1060 mbar (3000 m to –400 m)

Non-operating altitude range

500 mbar to 1060 mbar (5500 m to –400 m)

Fuses

2 × T4 AH; 250 VAC; 5 × 20 mm; breaking capacity 1500A @ 250 VAC; IEC, UL/CSA

Power requirements line voltage

100-240 VAC 50/60 Hz

Power consumption

200 VA

Cooling

Natural convection

Indicators

AC Power Present, Device ON

Degree of protection provided by enclosure

IP22

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Design, environmental, and physical specifications

Supplemental Information Manual

Display panel

19" LCD 5:4

Display panel resolution

1280 × 1024

Display panel contrast ratio

1000:1

Display panel viewing angle

170° vertical, 170° horizontal

Touch screen

Capacitive

USB 2.0 port connector

5 × USB type A

Equipotential connector

DIN 42801 equipotential ground stud

Video connector

DisplayPort

ePort interface connector

2 × ePort interfaces (RS232)

ePort interface communication type

100BASE-T and 10BASE-T

ePort interface power

Max 4.2 A, +15 to +17 VDC (single ePort) Max 6 A, +15 to +17 VDC (two ePorts combined)

Ethernet port

3 × (RJ45)

Ethernet port communication type

100BASE-T and 10BASE-T

Processor

Arm Cortex-A9

CARESCAPE Canvas Smart Display specifications WARNING INACCURATE RESULTS. Do not use or store the equipment outside the specified temperature, humidity, or altitude ranges, or outside the specified performance range. Using or storing the equipment outside the specified operating environment or outside the specified performance range may cause inaccurate results.

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Size (H × W × D)

388 × 440 × 126 mm

Weight

7.4 kg (16.3 lb)

Operating temperature range

10 to 40°C (50 to 104°F)

Non-operating temperature range

-20 to 60°C (-4 to 140°F)

Operating humidity range

15 to 90% RH non-condensing

Non-operating humidity range

10 to 90% RH non-condensing

Operating altitude range

700 mbar to 1060 mbar (3000 m to –400 m)

Non-operating altitude range

500 mbar to 1060 mbar (5500 m to –400 m)

Fuses

2 × T4 AH; 250 VAC; 5 × 20 mm; breaking capacity 1500A @ 250 VAC; IEC, UL/CSA

Power requirements line voltage

100-240 VAC 50/60 Hz

Power consumption

160 VA

Cooling

Natural convection

Indicators

AC Power Present, Device ON

Degree of protection provided by enclosure

IP22

ePort interface connector

One ePort interface

Display panel

19" LCD 5:4

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Design, environmental, and physical specifications

Display panel resolution

1280 × 1024

Display panel contrast ratio

1000:1

Display panel viewing angle

170° vertical, 170° horizontal

Touch screen

Capacitive

USB 2.0 port connector

3 × USB type A

Equipotential connector

DIN 42801 equipotential ground stud

ePort interface connector

1 × ePort interfaces (RS232)

ePort interface communication type

100BASE-T and 10BASE-T

ePort interface power

Max 4.2 A, +15 to +17 VDC

Ethernet port

2 × (RJ45)

Ethernet port communication type

100BASE-T and 10BASE-T

Processor

Arm Cortex-A9

CARESCAPE Canvas D19 display specifications WARNING INACCURATE RESULTS. Do not use or store the equipment outside the specified temperature, humidity, or altitude ranges, or outside the specified performance range. Using or storing the equipment outside the specified operating environment or outside the specified performance range may cause inaccurate results. Size (H × W × D)

388 × 440 × 126 mm

Weight

7.3 kg (16.1 lb)

Operating temperature range

10 to 40°C (50 to 104°F)

Non-operating temperature range

-20 to 60°C (-4 to 140°F)

Operating humidity range

15 to 90% RH non-condensing

Non-operating humidity range

10 to 90% RH non-condensing

Operating altitude range

700 mbar to 1060 mbar (3000 m to –400 m)

Non-operating altitude range

500 mbar to 1060 mbar (5500 m to –400 m)

Fuses

2 × T4 AH; 250 VAC; 5 × 20 mm; breaking capacity 1500A @ 250 VAC; IEC, UL/CSA

Power requirements line voltage

100-240 VAC 50/60 Hz

Power consumption

50 VA

Cooling

Natural convection

Indicators

AC Power Present, Device ON

Degree of protection provided by enclosure

IP22

Display panel

19" LCD 5:4

Display panel resolution

1280 × 1024

Display panel contrast ratio

1000:1

Display panel viewing angle

170° vertical, 170° horizontal

Touch screen

Capacitive

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