Sentec LuMon System User Manual
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Sentec LuMon System User Manual

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For the LuMon System
GUI software 1.0.x.x/TIC software 1.6.x.xxx
LuMon Belts / SensorBelt
for the LuMon System
2ST200-110 Rev 013 │2023-02

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Summary of Contents for Sentec LuMon System

  • Page 1 For the LuMon System GUI software 1.0.x.x/TIC software 1.6.x.xxx LuMon Belts / SensorBelt for the LuMon System 2ST200-110 Rev 013 │2023-02...
  • Page 2 Sentec AG are used, if the warranty seal on the lower side of the monitor is broken, or if...

  • Page 3: Table Of Contents

    ONITOR ON AND CHECKING ITS SYSTEM SETTINGS ..............................43 REOPERATIONAL CHECK ..............................44 INIMUM EQUIREMENTS BELT APPLICATION AND INITIATING MONITORING ....................45 ........45 ENSOR ELT APPLICATION AND INITIATING MONITORING FOR ADULTS AND CHILDREN for the LuMon System 3 of 93...
  • Page 4 ANNEX ......................................... 85 14.1 LMS ............... 85 RELATED CCESSORIES PARE ARTS AND OCUMENTS 14.2 T ..................................85 ERMINOLOGY 14.3 A ........................ 90 BBREVIATIONS USED IN THIS SER S UIDE 14.4 R ................................... 92 EFERENCES 4 of 93 for the LuMon System...

  • Page 5: Introduction

    NOTE The LuMon System is not intended for diagnosis, it is intended only as an adjunct in patient assessment. It must be used in conjunction with clinical signs and symptoms. The LuMon System comprises LuMon Monitors (5.1), belt connectors (5.2) to link Sentec belts (5.3) being available in various sizes to the LuMon Monitor, as well as Sentec contact agents/sprays (5.4)

  • Page 6: Symbols, Terminology And Abbreviations

    LuMon System indications and contraindications are provided in section 3. The principle of operation and limitations of EIT in general and Sentec EIT in particular are elucidated in 4. A brief description of the components of the LuMon System is provided in 5. Section describes the Graphical User Interface (GUI) of the LuMon Monitor.

  • Page 7: Safety Information

    Warnings and cautions WARNING The LuMon System is to be operated by qualified health care personnel. Personnel operating the LuMon System should have read and understood this manual, accessory directions for use, all precautionary information, and specifications before use. Improper use of the LuMon System may result in injury, inaccurate measurements and/or damage to the device.
  • Page 8 LuMon Monitors (particularly on the openings of its chassis), belt connectors, belts and other accessories. Neither immerse any parts of the LuMon System nor allow water or other liquids to enter the device. Failure to do so increases the risk of electrical shock and/or may result in damage to the device. If a LuMon Monitor has been wetted accidentally, it must be removed from AC mains power, wiped dry externally, allowed to dry thoroughly, and inspected by qualified technician (e.g.
  • Page 9 Before each use, prepare the LuMon System as described herein. Failure to do so increases the risk of cross contamination and patient infection.
  • Page 10 To avoid misinterpretation of results, it should be considered that the displayed Thorax Lung Contours EIT data associated thorax and lung models used by the LuMon System to evaluate the measured may deviate significantly from reality in case of patients with, for example, anatomic anomalies (e.g. after lung resection) or Thorax Lung Contours pathologies.

  • Page 11: Emc-Related Safety Information

    These substances can attack the device materials and device failure may result. CAUTION The LuMon System and its accessories are provided non-sterile. Do not sterilize any parts of the equipment by irradiation, steam or ethylene oxide. Do not autoclave or pressure sterilize.

  • Page 12: Glossary Of Symbols

    Do not use if package is damaged 60601-1) Dispose of according to Council Off (power) Directive 2012/19/EU On (power) Recommended user action(s) Information/instructions applicable to USB connection the Adults/Children configuration of LuMon System AC Power/Battery indicator 12 of 93 for the LuMon System...
  • Page 13 Safety Information Information/instructions applicable to Transport the Neonates/Infants configuration of LuMon System Storage Ingredients in INCI nomenclature Store in an upright position for the LuMon System 13 of 93...

  • Page 14: Indications And Contraindications

    The LuMon System provides no alarms and its measurements are only to be used as an adjunct to other clinical information. The LuMon System is not intended to be utilized as a primary vital signs monitor. The SensorBeltConnector and theThe LuMon Connector are reusable adapters intended to link a SensorBelt or a LuMon Belt to the LuMon Monitor.

  • Page 15: Principle Of Operation And Limitations

    RINCIPLE OF OPERATION AND LIMITATIONS General principle of operation Sentec EIT is based on the principles of Electrical Impedance Tomography (EIT), where weak alternating currents are applied and travel along the paths of least resistance through an object, and the electrical...

  • Page 16: Particular Features Of Sentec Eit

    Frerichs et al. [3], Putensen et al.[4], Lobo et al.[5]. Particular features of Sentec EIT Sentec EIT selects the thorax and lung models best adapted to the individual patient from a set of predefined, EIT image CT-derived thorax and lung models (9.1). These models are used for...
  • Page 17 (Table 13-13) and increases towards the central region of the thorax to reach a thickness of roughly one half to two-thirds of the thorax width. for the LuMon System 17 of 93...

  • Page 18: System Overview

    System overview YSTEM OVERVIEW This section provides a brief description of each component of the LuMon System (1.1), which is available in a configuration for adults and children and in a configuration for neonates and infants. The LuMon System comprises LuMon Monitors (5.1), belt connectors (5.2) to link Sentec belts (5.3) being available in various sizes to the LuMon Monitor, as well as Sentec contact agents/sprays (5.4)

  • Page 19: Belt Connectors

    SensorBeltConnector The SensorBeltConnector (Figure 5-3) links a SensorBelt (5.3.1) to a LuMon Monitor Adult (5.1). The position sensor embedded in its MatchBox permits the LuMon System to m position rotation inclination ) (9.2). If the SensorBeltConnector is properly connected to a LuMon Monitor in on- state, the status indicator LED of its MatchBox continuously lights green if a SensorBelt is connected.

  • Page 20: Belts

    LuMon Belt from its optimal position. The oblique design enables the LuMon Belt Adult to follow the movement of the ribs and thus does not restrict breathing. 20 of 93 for the LuMon System...

  • Page 21: Contact Agent/Spray

    5-7) are available in seven sizes (Table 13-14) and are intended for neonates and infants whose underbust girth is within approximately 17 to 52 cm. The embedded position sensor permits the LuMon System to measure and display the patien position ( rotation inclination ) (9.2).

  • Page 22: Measuring Tapes

    SensorBelt/LuMon Belt Adult size. Packaging labels of SensorBelts/LuMon Belt Adult size 92 exhibit an area with the same blue color. Refer to Table 13-14 for the full underbust girth range covered by each of the different available belts. 22 of 93 for the LuMon System...
  • Page 23 LuMon Belt size. Packaging labels of LuMon Belts size 35 exhibit an area with the same yellow color. Refer to Table 13-14 for the full underbust girth range covered by each of the different available belts for the LuMon System 23 of 93...

  • Page 24: Lumon Monitor Gui

    Figure 6-2: Activating the area of ScoutView belt (A1) or Refer to Figure 6-7 Figure 6-8 for a description of these areas. setti (A2) area Button Touching on this button activates or deactivates the area. 24 of 93 for the LuMon System...
  • Page 25 • the displayed time range of trends if a trend view (6.3.2, 6.3.4, 6.4.2) is active. Refer to Table 6-8 for the respective time ranges and the power-on default time range. for the LuMon System 25 of 93...
  • Page 26 , being Respiratory Rate displayed in larger size on the details view of VentView (Figure 6-13). Plethysmogram waveform Refer to Figure 6-13 for a description of this 26 of 93 for the LuMon System...

  • Page 27: Scoutview

    • displays the serial number (in case of SensorBelts) or lot number (in case of LuMon Belts) of the connected belt. for the LuMon System 27 of 93...
  • Page 28 To enable the selection of a new language, the LuMon Monitor must be restarted. NOTE EIT data stored in the LuMon Monitor date/time. No further operator confirmation will be requested at the time of the change. 28 of 93 for the LuMon System...

  • Page 29: Lufuview

    , trend and time range (here, the last button dimmed grey) Refer to Figure 6-5 for a description of the GUI elements being visible on all views for the LuMon System 29 of 93...
  • Page 30 Refer to Figure 6-4 for a description of the buttons Refer to Figure 6-5 for a description of the GUI elements being visible on all views 30 of 93 for the LuMon System...
  • Page 31 , trend and time range (here the last button dimmed grey) Refer to Figure 6-5 for a description of the GUI elements being visible on all views for the LuMon System 31 of 93...
  • Page 32 Refer to Figure 6-4 for a description of the buttons Refer to Figure 6-5 for a description of the GUI elements being visible on all views 32 of 93 for the LuMon System...

  • Page 33: Ventview

    Refer to Figure 6-4 for a description of the buttons details , trend and time range Refer to Figure 6-5 for a description of the GUI elements being visible on all views for the LuMon System 33 of 93...

  • Page 34: Common Aspects Of Eit Images And Trends

    EIT images rotate with the patient. • Thorax Contour rotation The thick grey line, being displayed at the irrespective of schematically visualizes the bed. • The black triangle points in direction of gravity. 34 of 93 for the LuMon System...
  • Page 35 T2 flag in one trend view, will also move the corresponding flag in the two other trend views to the same time. Dotted black vertical lines with triangles at both ends (if any) identify operator events (9.11). for the LuMon System 35 of 93...

  • Page 36: Visual Indicators

    2 electrodes in the belt Rotation indicates the right side of the patient 36 of 93 for the LuMon System...
  • Page 37 Displays if the LuMon System has detected a belt fault. Monitoring is not possible. Aside from the message, the LuMon System shows the identical behavior as if a belt connector is connected to the LuMon Monitor, but no belt is connected to the belt connector (6.6.3).
  • Page 38 (Figure 6-15)), Apart from the message, the behavior of the LuMon System is otherwise as if no belt connector is connected to the LuMon Monitor (6.6.3). Restart the LuMon Monitor. If this does not resolve the problem, contact a qualified technician, your local Sentec EIT representative or Sentec AG 6.6.3...
  • Page 39 Thorax Contour are highlighted red. Monitoring not possible (interrupted); signal quality The status message insufficient skin contact (6.6.2) is displayed and insufficient the image elements common to all EIT images (6.5.1) are blurred. for the LuMon System 39 of 93...

  • Page 40: Operator-Adjustable Parameters

    0 - 999 NOTE For the Adults/Children monitor configuration, the half underbust girth (e.g. from spine to sternum) is measured and entered; for the Neonates/Infants monitor configuration, the full underbust girth is measured and entered. 40 of 93 for the LuMon System...
  • Page 41 Analysis Mode 5/15/30 min 5 min Time range for trends 1/6/24 h Refer to Figure 6-4 for information on when new trend points are plotted. 10/30/60/300 s 30 s Time range for Plethysmogram for the LuMon System 41 of 93...

  • Page 42: Installation And Preoperational Check

    The LuMon Monitor (5.1) is a portable, bedside stand-alone EIT monitor. Optionally it can be mounted on Sentec Roll Stand for the LuMon Monitor (14.1) and on most VESA 75x75 mounts able to support at least 4 kg. To mount the LuMon Monitor on any of those mounting options use Sentec uMon VESA Screw Set (14.1) and refer to the instructions provided with the respective mounting options.

  • Page 43: Switching The Lumon Monitor On And Checking Its System Settings

    (Figure 6-6). Access system setting in ScoutView (Figure 6-8): • Check and if necessary, date/time with, for example, your inst date/time. • Verify that the field on the right of connector is empty. for the LuMon System 43 of 93...

  • Page 44: Minimum Requirements

    Hospitals and other heath care providers are responsible for preventing unauthorized access to the facility systems, devices and networks when installing the LuMon System. In case of doubt or any security issues, please consult your IT manager. 44 of 93 for the LuMon System...

  • Page 45: Belt Application And Initiating Monitoring

    Obtain a SensorBelt of the recommended size and open its package and place the SensorBelt with the striped fabric embedding the electrodes (Figure 5-5) facing upwards onto a flat surface. Figure 8-2 Applying ContactAgent to the striped fabric of a SensorBelt for the LuMon System 45 of 93...
  • Page 46 ScoutView (Figure 6-7) to select the thorax and lung model (9.1) best fitting the individual patient. Enter actual (not lean or ideal) body weight. Connect the SensorBeltConnector to the SensorBelt to initiate monitoring. 46 of 93 for the LuMon System...

  • Page 47: Lumon Belt Adult Application And Initiating Monitoring For Adults And Children

    Measuring tape Adults/Children indicate the size of the recommended LuMon Belt. To assist size selection, packaging labels of correspondingly sized belts exhibit an area with the same color. Refer to Table 13-14 for available LuMon Belt sizes. for the LuMon System 47 of 93...
  • Page 48 Make sure the belt follows the ribs along the 5th/6th ICS on an oblique plane with the with the top- end of the mid-line of the LuMon Belt skin but does not restrict breathing. • Then connect the LuMon Belt with the LuMon Connector. 48 of 93 for the LuMon System...

  • Page 49: Lumon Belt Neo Application And Initiating Monitoring For Neonates And Infants

    Belts sizes. Obtain a LuMon Belt of the recommended size, open its package and place the LuMon Belt with the striped fabric embedding the electrodes (Figure 5-7) facing upwards onto a flat surface. for the LuMon System 49 of 93...
  • Page 50 Analysis Mode Check proper setup (8.4) and adequacy of the selected being adequate breathing pattern (8.5) initially and at least every 8 hours while monitoring the patient (9). 50 of 93 for the LuMon System...

  • Page 51: Checking The Proper Setup

    (ICS) on an oblique plane with the top-end of the mid-line of the LuMon Belt Checking for correct data entry on monitor for adults and children Verify that the half underbust girth and patient data entries on the monitor correspond to those of the actual patient. for the LuMon System 51 of 93...
  • Page 52 In case of interferences from other devices switch off the other device (if possible) or in case of impedance respiration monitoring through ECG electrodes, reposition the electrodes further away from the belt. If this does not resolve the problem, contact a qualified technician, your local Sentec EIT representative or Sentec AG.
  • Page 53 If this does not resolve the problem, remove the belt, re-apply contact agent/spray to the striped fabric of the belt and re-initiate monitoring (10.2). for the LuMon System 53 of 93...
  • Page 54 In case of interferences from other devices switch off the other device (if possible) or in case of impedance respiration monitoring through ECG electrodes, reposition the electrodes further away from the belt. If this does not resolve the problem, contact a qualified technician, your local Sentec EIT representative or Sentec AG.

  • Page 55: Checking The Adequacy Of The Selected Analysis Mode

    BB mode is adequate to analyze episodes during which the Plethysmogram (9.4) reflects quite regular breathing, basically, when most breaths can be detected (9.5) reliably and RRi values (9.6) are frequently for the LuMon System 55 of 93...
  • Page 56 The less regular and/or Lung Impedance the weaker breathing-related changes are, the fewer breaths the LuMon System detects BB mode and the less appropriate the selection of TB-I mode is adequate to analyze episodes during which the minima and maxima of the Plethysmogram (9.4)
  • Page 57 In this case, consider using NOTE Analysis Mode Irrespective of the currently selected , the LuMon System in the background permanently EIT raw data Analysis Modes analyzes the measured with all and stores or outputs the results obtained with each Analysis Mode mode.

  • Page 58: While Monitoring The Patient

    Monitor in the on-state (8). NOTE The LuMon System is not intended for diagnosis, it is intended only as an adjunct in patient assessment. It must be used in conjunction with other clinical signs and symptoms. As an introduction to this section, sub-sections 9.1, 9.2, and address several particular features of the LuMon System or more generally Sentec EIT.

  • Page 59: Accounting For The Patient S Position

    The thorax and lung models used by the LuMon System also assume specific positions of the 32 electrodes on horax. In order to obtain optimal data, it is therefore very important to apply belts of recommended size to the patient properly (8) and to check belt positioning regularly (at least every 8 hours) during monitoring (8.4).

  • Page 60: Quality Of Calculated Eit Data

    . This is, for example, the case, if the patient is standing or sitting upright. Quality of calculated EIT data EIT raw data EIT images The LuMon System continuously evaluates the quality of the measured and of the indices Respiratory Rate derived thereof.

  • Page 61: Global Dynamic Images And Plethysmogram

    -- . In conditions in which monitoring is possible, but the LuMon System is unable to detect a breath (9.5) or if the Respiratory Rate is outside its specified display range (13.1), the last calculated...
  • Page 62 If exhaling against ambient pressure the local minima that will be observable in the Plethysmogram , for example, will be related to the functional residual capacity (FRC) during normal breathing, or to the residual volume (RV) after a forced full expiration. 62 of 93 for the LuMon System...

  • Page 63: Breath Detection

    (HFOV) or under other high-frequency ventilation modalities. NOTE The ability of the LuMon System to detect lung volume changes depends on the dimension of the lung with respect to the thorax. As this relationship is similar across all age groups, the LuMon System can detect much smaller absolute lung volume changes in neonates than in adult patients.

  • Page 64: Respiratory Rate

    RRi value is a moving average over the last four detected breaths. If the LuMon System is unable to detect a breath, for example if a patient is breathing rather shallowly, or if the Respiratory Rate...
  • Page 65 While monitoring the patient NOTE Analysis Mode Irrespective of the currently selected , the LuMon System in the background permanently EIT raw data Analysis Modes analyzes the measured with all and stores or outputs the results obtained with each Analysis Mode mode.

  • Page 66: Trends Of Eeli, Eili And Aeration

    In BB mode and as illustrated in Figure 9-9 for the last detected breath, EELI corresponds to measured at the beginning and the end of detected breaths, i.e. at start inspiratory respectively end-expiratory 66 of 93 for the LuMon System...

  • Page 67: Stretch Image Relative Tidal Stretch

    • by first subtracting the EELI distribution (on the right) from the EILI distribution (on the left) (yielding Lung Impedance as an intermediate result the change in distribution between the respective time points), for the LuMon System 67 of 93...
  • Page 68 Relative Tidal Stretch about both the center and the spread of weighted Figure 9-15: Example of a Stretch Image and of the associated weighted Relative Tidal Stretch histogram. 68 of 93 for the LuMon System...

  • Page 69: Center Of Ventilation, Silent Spaces And Functional Lung Spaces

    (i.e. towards the right lung if the patient is in supine position and towards the left lung if the patient is in prone position). Figure 9-17: Coordinates of the CoV for the LuMon System 69 of 93...

  • Page 70: Operator Events And Screenshots

    CoV(h) are always automatically defined if changes, thereby allowing to directly assess the influence of ventilation distribution. Only in supine position, the coordinates CoV(v) and CoV(h) used by the LuMon System are ali body directions typically used in literature [3],...

  • Page 71: Recording Or Exporting Data

    In long recordings (>15 minutes), the recorded data might extend over multiple files to avoid excessively large file handling. NOTE Analysis Mode Irrespective of the currently selected (9.7), the LuMon System in the background permanently analyzes the measured EIT raw data with all Analysis Modes and stores or outputs the results obtained with each mode.
  • Page 72 *.lbk) file may also be used for troubleshooting purposes (12) and you may be asked to send it to Sentec. Other than the gender, weight, height, and underbust girth, it does not contain patient data. NOTE...

  • Page 73: Pausing Or Ending Monitoring

    If desired, review or export trend data (9.11) for the monitored patient before turning off the monitor. • Switch the monitor off and perform cleaning and disinfection actions (11.2) on the LuMon Monitor and belt connector before use on the next patient (7.4). for the LuMon System 73 of 93...

  • Page 74: Maintenance

    • Check the LuMon Monitor, its power cord and the belt connector for mechanical or functional damage at least once a month. Replace any defective parts with Sentec original parts. Refer to 11.3 replace the fuses of the LuMon Monitor.
  • Page 75 These substances can attack the device materials and device failure may result. CAUTION The LuMon System and its accessories are provided non-sterile. Do not sterilize any parts of the equipment by irradiation, steam or ethylene oxide. Do not autoclave or pressure sterilize.

  • Page 76: Replacing The Fuses Of The Lumon Monitor

    Please contact your local Sentec EIT representative or Sentec AG prior to returning any material. The following instructions apply to all shipments of the LuMon System or any part of it to your local Sentec EIT representative or Sentec AG: •...

  • Page 77: Troubleshooting

    11.5. NOTE Detailed troubleshooting is provided in the Service Manual for the LuMon System. It describes problems, Sentec possible causes and the recommended corrective action(s) the operator, qualified technicians or Authorized LuMon Technicians may perform to resolve the problem.

  • Page 78: Technical Specifications

    (BMI) in Adults/Children configuration. In Neonates/Infants configuration, where only one CT-derived model is used, the LuMon System accounts for the displacement of the electrodes around the thorax from their assumed default positions.
  • Page 79 LuMon Connector IPX1 Table 13-5: Intra-system compatibilities System Intra-system compatibilities LuMon Monitors supports SensorBeltConnectors and SensorBelts OR LuMon Connectors and LuMon Belts Adult Adult LuMon Monitors only support LuMon Connectors and LuMon Belts Neo for the LuMon System 79 of 93...

  • Page 80: Lumon Monitor

    Technical specifications 13.2.1 Compliance/standards The LuMon System was developed in accordance with following standards. Table 13-6: Compliance/standards Properties Parts Standards Safety approvals IEC 60601-1 Electromagnetic LuMon Monitor IEC 60601-1-2 compatibility (EMC) SensorBeltConnector/LuMon Connector SensorBelt/LuMon Belt Applied part BF SensorBelt/LuMon Belt...

  • Page 81: Belt Connectors

    Length of cable Approximately 2.5 m Approximately 2.5 m Compatibility LuMon Monitor - Adult LuMon Monitor - Neo SensorBelts LuMon Belts Figure 13-2: Dimensions of the SensorBeltConnector Figure 13-3: Dimensions of the LuMon Connector for the LuMon System 81 of 93...

  • Page 82: Belts

    According to the European directive 93/42/EEC and the European Regulation 2017/745 • LuMon Monitor, SensorBeltConnector and LuMon Connector are classified as Class IIa devices. • SensorBelt, LuMon Belts, ContactAgent/LuMon Contact Spray and NeoContactAgent are classified as Class I devices. 82 of 93 for the LuMon System...

  • Page 83: Emc Declaration

    IEC 61000-4-8 Portable and mobile RF communications equipment should be used no closer to any part of the LuMon System, including cables, than the recommended separation distance d calculated from the equation applicable to the frequency of the transmitter.
  • Page 84 RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the LuMon System is used exceeds the applicable RF compliance level above, the LuMon System should be observed to verify normal operation.

  • Page 85: Annex

    LMS related Accessories, Key Spare Parts and Documents WARNING Use only equipment, accessories, disposables or parts supplied or recommended by Sentec AG. Use of other parts may result in injury, inaccurate measurements and/or damage to the device. Table 14-1: Part numbers Key Spare parts...
  • Page 86 The remaining time a belt can be used. When a new belt is connected to a LuMon System, a timer begins to count down from the preset belt time to zero. The countdown interrupts if the belt is disconnected and resumes when reconnected.
  • Page 87 (HoV) certain EIT images corresponds to the line of intersection of the belt plane with each rotation change the HoV. TB-I modes. EIT images HoV divides into non-dependent (upper part of image) and for the LuMon System 87 of 93...
  • Page 88 EIT raw data A typically numeric physiological variable that can be derived from and validated against a clinical reference method. Respiratory Rate Currently, the only example in the LuMon System is the Plethysmogram Waveform representing relative Lung Impedance variations over time.
  • Page 89 Authorized completed a LuMon System LuMon (documented by a respective certification issued by Sentec EIT (or a hereto Technician authorized third-party)) to perform repair procedures for the LuMon Monitor that do require opening of its cover and to install software updates and software upgrades on LuMon Monitors.

  • Page 90: Abbreviations Used In This User S Guide

    Annex 14.3 Abbreviations Abbreviations are sorted alphabetically: 14.3.1 Abbreviations related to Sentec EIT, EIT in general and clinical terms Breath-based LuMon Connector Body mass index LMCS LuMon Contact Spray LuMon System breaths per minute ContactAgent LMS-A LuMon System - Adults/Children...
  • Page 91 Means of Patient Protection (electrical WEEE Waste electrical and electronic safety standard) equipment Local area network Symbol for microtesla (unit of magnetic µt flux density) Pounds per square inch Radio frequency Root mean square for the LuMon System 91 of 93...

  • Page 92: References

    Respir Med. 2017; 12:3. Frerichs Respir Crit Care Med. 2020; 201(3):386-8. [10] estimation of recruitable alveolar collapse and hyperdistension by electrical impedance [11] -60. [12] collapse and hypoxemia in early Care Med. 2006; 174(3):268-78. 92 of 93 Guide LuMon System...
  • Page 93 PLEASE CONTACT US, IF YOU HAVE ANY QUESTIONS! Manufacturer: Sentec AG | Kantonsstrasse 14 | 7302 Landquart | Switzerland | www.Sentec.com | Phone: +41(0)81 330 09 70 | Fax: +41(0)81 330 09 71 | info-eit@Sentec.com for the LuMon System 93 of 93...

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