Weinmann MEDUCORE Standard2 Instructions For Use Manual
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Weinmann MEDUCORE Standard2 Instructions For Use Manual

Monitor/defibrillator
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MEDUCORE Standard
Monitor/Defibrillator
Instructions for Use for Devices from Software Version 1.1

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Summary of Contents for Weinmann MEDUCORE Standard2

  • Page 1 MEDUCORE Standard Monitor/Defibrillator Instructions for Use for Devices from Software Version 1.1...

  • Page 2: Table Of Contents

    Table of Contents Table of Contents Introduction Intended use ................. 6 Function ..................6 Operator/user qualification ............8 Contraindications for defibrillation ..........8 Side effects ................... 9 Safety Safety information ............... 10 General instructions ..............24 Warnings in this document ............25 Description Overview ..................
  • Page 3 Table of Contents Operation Switching the device on ............... 76 Switching the device off .............. 77 Navigating in the device .............. 77 Selecting the patient group ............78 Performing defibrillation .............. 80 Performing pulse oximetry monitoring .......... 89 Performing ECG monitoring ............90 Performing non-invasive blood pressure measurement (NIBP) ..
  • Page 4 Table of Contents NIBP settings ................134 System settings ................. 137 Device information ..............142 Hygienic reprocessing General instructions ..............144 Intervals ..................145 Hygienic reprocessing of the device ........... 145 Function check 10.1 Intervals ..................148 10.2 Performing a function check ............148 10.3 Checking the ECG cables ............
  • Page 5 Table of Contents 15.5 CARDIObiphasic defibrillation system ......... 179 15.6 ECG monitoring system ............. 180 15.7 ECG analysis system CARDIOlogic ..........181 15.8 Pulse oximetry monitoring ............182 15.9 Non-invasive blood pressure (NIBP) monitoring ......183 15.10 Operation/data management ............. 184 15.11 Alarm delay times ..............

  • Page 6: Introduction

    1 Introduction Introduction 1.1 Intended use MEDUCORE Standard is a mobile external defibrillator with monitoring functions. It is used to measure and monitor vital parameters and for defibrillation of emergency patients. The following monitoring and diagnostic functions are available: • 6-lead monitoring ECG •...
  • Page 7 1 Introduction • Pulse oximetry: Pulse oximetry monitoring allows continuous, non-invasive measurement of the arterial oxygen saturation with the aid of different pulse oximetry sensors for different application sites. At the same time, a photo sensor in the pulse oximetry sensor registers the percentage of oxygenated hemoglobin in the arterial blood (SpO ) using different light wavelengths.

  • Page 8: Operator/User Qualification

    (Medizinprodukte-Betreiberverordnung)). General recommendation: You should seek instruction on the correct handling, use and operation of this medical device from a person authorized by WEINMANN Emergency. 1.4 Contraindications for defibrillation Defibrillation must only be performed in cases of: •...

  • Page 9: Side Effects

    1 Introduction 1.5 Side effects Possible side-effects of defibrillation are: • Burns • Arrhythmias triggered by defibrillation • Ventricular fibrillation • Failure of active implants • Skin irritations • Failure of external diagnostic or therapy devices MEDUCORE Standard...

  • Page 10: Safety

    2 Safety Safety 2.1 Safety information Read these Instructions for Use carefully. They form part of the devices described, and must be available at all times. Only use the device for the intended use (see "1.1 Intended use", page For your own safety and that of your patients, and in accordance with the requirements of Directive 93/42/EEC, please observe the following safety instructions.
  • Page 11 2 Safety Risk of injury due to device or component malfunction! A damaged device or damaged components may result in injury to the patient, user or bystanders. ⇒ Only operate the device and components if they are externally undamaged. ⇒ Only operate the device and components if the function check has been successfully completed.
  • Page 12 Risk of injury from using third-party accessories! Accessories which have not been approved by WEINMANN Emergency can result in electric shocks, incorrect monitoring, negative impact on interference immunity and emission or lead to damage to the device and injure the patient.
  • Page 13 ⇒ Do not open the device. ⇒ The device should only be opened by WEINMANN Emergency or persons authorized by WEINMANN Emergency. ⇒ Measures such as repairs and maintenance should only be carried out by the manufacturer or by a technician expressly authorized by the latter.
  • Page 14 2 Safety ⇒ Always have a charged, ready-to-use spare battery on hand. Caution Risk of injury from touching the contacts in the battery compartment and the patient at the same time! The contacts in the battery compartment are live. Touching the contacts and the patient at the same time can injure the user or the patient.
  • Page 15 2 Safety 2.1.4 Defibrillation Warning Risk of injury due to sparks during defibrillation in the presence of oxygen and combustible materials! During defibrillation in an oxygen-enriched atmosphere and in the presence of combustible materials (e.g. textiles), sparks generated by defibrillation may cause explosion and fire, which may result in injury to the patient, user or bystanders.
  • Page 16 2 Safety ⇒ Only perform defibrillation on patients who are not responding normally, are not breathing normally and have a defibrillatable cardiac rhythm. Risk of injury due to unsuitable AED analysis algorithm in children below one year of age! The device's AED analysis algorithm is not designed for children below one year of age and may result in injury to the child.
  • Page 17 ⇒ Dispose of defibrillation electrodes after use, and do not reuse them. ⇒ Only use defibrillation electrodes approved by WEINMANN Emergency for the device. Risk of injury and delay in treatment due to implanted cardiac pacemakers! Impulses from implanted cardiac pacemakers may affect the detection of defibrillatable cardiac rhythms, and delay treatment.
  • Page 18 2 Safety Risk of injury due to ECG misinterpretation if ECG is derived from the defibrillation electrodes! If the ECG is derived from the defibrillation electrodes, the device shows a non-diagnostic ECG curve. The ECG curve is designed to detect shockable cardiac rhythms and is not suitable for differential diagnostics.
  • Page 19 ⇒ Use ECG electrodes WM 45201 which have been approved by WEINMANN Emergency. If this is not possible: Only use ECG electrodes which satisfy all the of the following points. ⇒ Only use ECG electrodes as per AAMI EC 12.
  • Page 20 2 Safety Caution Risk of injury due to ECG malfunction in the vicinity of electrosurgical devices! ECG functions may be affected by electrosurgical devices and result in injury to the patient. ⇒ Only use approved ECG cables. Risk of injury from burns during defibrillation! ECG cables without defibrillation protection may result in injury to the patient.
  • Page 21 2 Safety ⇒ Avoid strong movement of the pulse oximetry sensor. If necessary: To relieve strain, loop the pulse oximetry sensor cable and the pulse oximetry sensor connecting cable and fix to the patient with a plaster. ⇒ Do not attach the pulse oximetry sensor to a limb on which there is already an NIBP sleeve or catheter port.
  • Page 22 ⇒ Do not stack the device with other medical electrical devices. ⇒ Do not operate the device in the direct vicinity of other medical electrical devices (exception: Approved combinations of devices for MEDUCORE Standard on the portable systems from WEINMANN Emergency). MEDUCORE Standard...
  • Page 23 This can injure the patient. ⇒ Only use the articles defined by WEINMANN Emergency in the scope of supply and accessories. Risk of injury from portable radio-frequency communication devices in the immediate vicinity of the device! Portable radio-frequency communication devices (e.g.

  • Page 24: General Instructions

    • Repairs, servicing and maintenance should only be carried out by the manufacturer WEINMANN Emergency or by a technician expressly authorized by the latter. • The manufacturer, WEINMANN Emergency, guarantees the compatibility of the device and all components or accessories connected to the patient prior to use.

  • Page 25: Warnings In This Document

    2 Safety • This device’s software contains code which is subject to the General Public License (GPL). You will receive the source code and the GPL upon request. 2.3 Warnings in this document Warnings are used to flag up safety-relevant information. You will find a warning preceding any action that entails a hazard for persons or equipment.

  • Page 26: Description

    3 Description Description 3.1 Overview 3-1 Device Designation Description ECG connection for ECG cable Connects the device to the ECG cable. Displays settings and current values (see "3.4 Symbols Display on the display", page 37). Alarm light Indicates high-priority alarms visually. Power supply connection Connects the device to the power supply.

  • Page 27: Control Panel

    3 Description Designation Description Connects the device to an NIBP cuff via the NIBP Connection for NIBP connecting tube connecting tube. Battery compartment with battery Houses the battery. 3.2 Control panel 3-2 Controls Designation Description Line power indicator Indicates that the device is connected to line power. •...
  • Page 28 3 Description Designation Description • Pauses the audio alarm output for a certain length of time. • Mutes the audio alarm output. Alarm button • Cancels audio alarm outputs. • Deactivates muting of the audio alarm output and alarm cancellation. •...

  • Page 29: Display

    3 Description 3.3 Display 3.3.1 Start menu 3-3 Start menu display Designation Description Battery status Displays the charge level of the battery. Time Displays the time. Service reminder (if activated) Displayed when the service interval is ≤ 30 days. Starts the device with the presets specific to the Patient groups patient groups.
  • Page 30 3 Description 3.3.2 AED mode 3-4 Display in AED mode: Parameter view (top) and curve view (bottom) Designation Description Battery status Displays the charge level of the battery. Time Displays the time. Session duration Displays the duration of the current session. Displays the number of shocks delivered during the Number of shocks delivered current session.
  • Page 31 3 Description Designation Description Shows the selected patient group: Patient group • for adults • Child Mode indicator Indicates the currently selected mode. Alarm limits Displays the set alarm limits. Shows whether the alarm output is deactivated in AED Alarm off indicator mode.
  • Page 32 3 Description 3.3.3 Manual mode 3-5 Display in manual mode Designation Description Battery status Displays the charge level of the battery. Time Displays the time. Session duration Displays the duration of the current session. Displays the elapsed device time since the last Elapsed time since last defibrillation defibrillation.
  • Page 33 3 Description Designation Description Enables the user to select the type of ECG lead ECG lead selection displayed in the middle curve field (I, II, III, aVR, aVL or aVF). Monitor mode Provides access to the monitor mode. Charging Charges the defibrillation capacitor. Shows the curve corresponding to 1 mV of the ECG ECG calibration mark signal.
  • Page 34 3 Description 3.3.4 Monitor mode 3-6 Display in monitor mode: Parameter view (top) and curve view (bottom) Designation Description Battery status Displays the charge level of the battery. Time Displays the time. Indicates the status of the audio alarm output: •...
  • Page 35 3 Description Designation Description Shows the selected patient group: • for adults Patient group • Child • Infant Mode indicator Indicates the currently selected mode. Alarm limits Displays the set alarm limits. Shows the time and values of the last NIBP History measurements.
  • Page 36 3 Description 3.3.5 NIBP function mode 3-7 Display in monitor mode with superimposed NIBP function mode Designation Description Shows the time and values of the last three NIBP History measurements. • Starts or stops an NIBP measurement. Start/stop • Starts or stops an interval measurement. •...

  • Page 37: Symbols On The Display

    3 Description Designation Description Shows the alarm limits for the systolic and diastolic Alarm limits measured values. Shows the systolic value with an NIBP measurement. Shows the diastolic value with an NIBP measurement. 3.4 Symbols on the display Symbol Designation Description Battery status symbol Battery status...
  • Page 38 3 Description Symbol Designation Description Heart rate tone/pulse tone on Heart rate tone/pulse tone function button Heart rate tone/pulse tone off Requirements for function check met Requirements for function check not met Function check symbols Fault found during function check Follow Instructions for Use Service interval exceeded •...

  • Page 39: Battery And Battery Status Indicator

    3 Description 3.5 Battery and battery status indicator 3-8 Battery and battery status indicator Designation Description Battery Supplies power to the device. Fault indicator (red) Lights up if the battery is defective. Status LEDs (green) Show the battery status. Status button Activated by pressing the status LEDs.
  • Page 40 3 Description Status indicator on Status indicator on Meaning the battery the device display Battery status < 10% On the display: • The last remaining segment in the battery status symbol is red. • The message Battery weak appears in the display.

  • Page 41: Components

    3 Description 3.6 Components 3-9 Components Designation Description ® SoftTip pulse oximetry sensor, size M, Measures oxygen saturation. reusable Pulse oximetry sensor connecting cable Connects the pulse oximetry sensor to the device. Connects the pulse oximetry sensor to the device via connector the pulse oximetry connecting cable.
  • Page 42 3 Description Designation Description Connects the defibrillation electrodes and the Trunk cable function test resistor to the device. SD card Records session data. NIBP connecting tube Connects the NIBP cuff to the device. NIBP cuff, adult, for 23-33 cm upper arm For measuring patient’s blood pressure.

  • Page 43: Accessories

    3 Description 3.7 Accessories 3-10 Accessories MEDUCORE Standard...
  • Page 44 3 Description Designation Description Charging station for battery WM 45045 Allows external battery charging. Protects the device against damage and facilitates Protective transport bag transportation. Conducts the electrocardiograms to the device. ECG cable Available in various designs (see "16.3 Accessories", page 191).

  • Page 45: Transport Options

    3 Description 3.8 Transport options 3-11 Transport options (examples) In order to transport the device, carry accessories, provide a charging voltage and attach to a wall mounting, you can mount the device on one of the following portable systems: • LIFE-BASE 3 NG •...

  • Page 46: Markings And Symbols

    3 Description 3.10 Markings and symbols 3.10.1 Markings on the device 3-12 Markings on the product Symbol Description Device information label Serial number Input (12 V-15 V, 30 W) Direct voltage Maximum energy generated = 200 J Do not dispose of device in household waste Type of protection against electric shock: Protection class II device MEDUCORE Standard...
  • Page 47 3 Description Symbol Description Date of manufacture Degree of protection against • Ingress of solid objects IP55 • Ingress of dust • Ingress of water with harmful effect Follow Instructions for Use CE mark (confirms that the product complies with the applicable European directives) Other labels and symbols Safety check label (only in the Federal Republic of Germany): Indicates when...
  • Page 48 3 Description 3.10.2 Markings on the battery 3-13 Markings on the battery Symbol Description Battery fault, if fault indicator light is red Battery status Follow Instructions for Use Manufacturer Do not dispose of in household waste. China RoHS label (confirms that the product does not emit toxic substances for the number of years indicated) MEDUCORE Standard...
  • Page 49 3 Description 3.10.3 Markings on the pulse oximetry sensors Symbol Description Follow Instructions for Use Do not dispose of in household waste. Manufacturer 3.10.4 Markings on the ECG cable Symbol Description Follow Instructions for Use Do not dispose of in household waste. 3.10.5 Markings on the defibrillation electrodes Follow the Instructions for Use for the defibrillation electrodes.
  • Page 50 3 Description 3.10.7 Markings on the packaging Symbol Description Device packaging Article number Permissible storage temperature: -40 °C to +70 °C Permissible storage humidity: 15 % to 95 % relative humidity Keep dry Fragile Follow Instructions for Use Serial number CE mark (confirms that the product complies with the applicable European directives) Manufacturer Battery packaging...
  • Page 51 3 Description Symbol Description sensor packaging Do not dispose of in household waste. Non-sterile Latex-free Permissible storage humidity: Max. 95 % relative humidity Permissible storage temperature: -40 °C to +70 °C Degree of protection against temporary immersion in water IPX7 Degree of protection against water dripping at an angle, 15°...
  • Page 52 3 Description Symbol Description ECG cable packaging Permissible storage temperature: -40 °C to +70 °C Permissible storage humidity: Max. 95 % relative humidity Do not dispose of in household waste Article number Serial number Follow Instructions for Use Manufacturer Date of manufacture NIBP cuff packaging Follow the Instructions for Use for the NIBP cuffs.

  • Page 53: Preparation

    4 Preparation Preparation 4.1 Mounting the device The device is mounted on a portable system as standard and is ready for use. Follow the Instructions for Use for the portable systems. 4.2 Connecting to a power supply Risk of injury due to missing battery! During line operation, defibrillation is not possible without the battery.

  • Page 54: Using The Rechargeable Battery

    4 Preparation 3. Slide the fully charged battery into the battery compartment until it clicks into place. 4. If necessary: If operating on the portable system, mount the portable system on a wall mounting with charging interface Connect the device with its power supply unit and charger to the line power.
  • Page 55 4 Preparation • Note the methods of storing the battery and the charging intervals for prolonged storage (see "13.3 Storing the battery", page 173). • The expected life of the battery is 2 years. Recommendation: Replace the battery after 2 years. If battery life has substantially dropped before then, replace the battery earlier.
  • Page 56 4 Preparation 2. When the battery status indicator lights up green and/or the symbol appears on the display: Disconnect the device from the charging interface or from the power supply unit and charger. Result The battery is fully charged. 4.3.3 Charging the battery with the charging station You can also charge the battery with the charging station WM 45190.

  • Page 57: Connecting The Trunk Cable And Defibrillation Electrodes

    4 Preparation 4.4 Connecting the trunk cable and defibrillation electrodes Damage to the device caused by ingress of liquids! The device is only protected from water jets as per IP55 when the battery is inserted, the water jet protection for the SD card slot is closed and the lines for the ECG, SpO , trunk cable and NIBP connecting tube including NIBP cuff are connected.
  • Page 58 4 Preparation Risk of injury due to incorrectly selected size of defibrillation electrodes! If the wrong size of defibrillation electrodes is selected, this can result in sub-optimal defibrillation results and patient burns. ⇒ Select the correct size of defibrillation electrodes pursuant to the resuscitation guidelines and not based on the weight specifications given on the packaging.
  • Page 59 4 Preparation 5. Select the required electrode position on the patient's torso: • Position 1: Sternum-apex • Position 2: Anterior-posterior (can also be used for adults) Risk of injury due to air/moisture between defibrillation electrodes and the patient's skin! Air (e.g. in hirsute patients) or moisture between the defibrillation electrodes and the patient's skin prevent correct shock delivery and may result in burns to the skin and unsuccessful defibrillation.

  • Page 60: Connecting The Pulse Oximetry Sensor

    4 Preparation 4.5 Connecting the pulse oximetry sensor Damage to the device caused by ingress of liquids! The device is only protected from water jets as per IP55 when the battery is inserted, the water jet protection for the SD card slot is closed and the lines for the ECG, SpO , trunk cable and NIBP connecting tube including NIBP cuff are connected.
  • Page 61 4 Preparation Pulse oximetry sensor Patient group Application site Disposable sensor for adults > 30 kg body weight (Adult) Disposable sensor for children 10 kg-50 kg body weight Finger/large toe (Pediatric) Disposable sensor for infants 10 kg-20 kg body weight (Infant) 3.
  • Page 62 4 Preparation 7. Attach the pulse oximetry sensor: Pulse oximetry Attachment sensor ® SoftTip sensor Special feature: The finger mark must point upwards Wrap sensor Special feature: The sensor's transmitter and receiver must be aligned to face each other on one axis.
  • Page 63 4 Preparation Pulse oximetry Attachment sensor Disposable sensor Special feature: The sensor's transmitter and receiver must be aligned to face each other on one axis. When doing so, please note: • The site must have a good blood supply. • When attaching to the finger: If possible, use the ring or middle finger of the non-dominant hand.

  • Page 64: Connecting The Ecg Cable And Ecg Electrodes

    4 Preparation 4.6 Connecting the ECG cable and ECG electrodes Damage to the device caused by ingress of liquids! The device is only protected from water jets as per IP55 when the battery is inserted, the water jet protection for the SD card slot is closed and the lines for the ECG, SpO , trunk cable and NIBP connecting tube including NIBP cuff are connected.
  • Page 65 4 Preparation Risk of injury due to air/moisture between ECG electrodes and the patient's skin! Air (e.g. in the case of hirsute patients) or moisture between the ECG electrodes and the patient's skin impair the quality of the ECG signal and falsify the measurement results. This can injure the patient.
  • Page 66 4 Preparation 7. Stick and firmly press on the ECG electrodes as follows: Code 1 (Europe) Code 2 (America) Electrode Electrode Color coding Color coding Application site marking marking Right arm; shortened: White under right collarbone Left arm; shortened: Yellow Black under left collarbone Left leg;...
  • Page 67 4 Preparation R/RA L/LA N/RL F/LL 4-2 Shortened position for ECG electrodes 8. If the ECG electrodes are used at the same time as the defibrillation electrodes: Do not allow ECG electrodes and defibrillation electrodes to overlap. 9. If necessary: Stroke out any trapped air from under the ECG electrodes.

  • Page 68: Attaching The Nibp Cuff

    4 Preparation 4.7 Attaching the NIBP cuff Damage to the device caused by ingress of liquids! The device is only protected from water jets as per IP55 when the battery is inserted, the water jet protection for the SD card slot is closed and the lines for the ECG, SpO , trunk cable and NIBP connecting tube including NIBP cuff are connected.
  • Page 69 4 Preparation Risk of injury due to incorrect NIBP cuff! An incorrectly selected or used NIBP cuff can lead to patient injuries. ⇒ Attach the NIBP cuff so that the blood supply is not stopped. ⇒ Do not attach the NIBP cuff to a limb with an intravenous infusion.
  • Page 70 4 Preparation When doing so, please note: Select a Right size Select a smaller one larger one RANGE • The index printed on the NIBP cuff must be within the printed range. • If the index marking does not extend into the printed range: Select a larger NIBP cuff.
  • Page 71 4 Preparation 5. Connect the NIBP connecting tube to the tube of the NIBP cuff. 6. Turn the two tubes towards each other until they lock into place. Risk of injury due to incorrectly attached NIBP cuff! An incorrectly attached NIBP cuff can result in excessive contact pressure.
  • Page 72 4 Preparation 7. Attach the empty NIBP cuff to fit closely around the patient's limb. When doing so, please note: • The skin below the NIBP cuff must be undamaged. • The NIBP cuff must fit tightly around the limb. •...

  • Page 73: Using The Sd Card

    4 Preparation 4.8 Using the SD card Loss of data due to incorrect SD card! SD cards not purchased from WEINMANN Emergency may have reduced functionality or result in the loss of data. ⇒ Only use SD cards from WEINMANN Emergency.
  • Page 74 4 Preparation 2. Push the SD card into the SD card slot until it clicks into place. When doing so, please note: The beveled corner of the SD card must be at the front on the right during insertion. 3. Close the water jet protection to protect the device from the ingress of dust and water.
  • Page 75 4 Preparation Result The SD card is removed. The symbol appears on the device display. MEDUCORE Standard...

  • Page 76: Operation

    5 Operation Operation 5.1 Switching the device on Requirement • The ECG cable and the defibrillation electrodes are not connected to the patient. • A fully charged battery is inserted in the device. 1. Briefly press the On/Off button An automatic self-test starts, which runs through the following sequence: •...

  • Page 77: Switching The Device Off

    5 Operation Result The device is switched on. 5.2 Switching the device off 1. Press and hold the On/Off button for at least 2 seconds. Result The device is completely switched off. 5.3 Navigating in the device Result Action Within a menu In the start In a menu In a mode...

  • Page 78: Selecting The Patient Group

    5 Operation Result Action Within a menu In the start In a menu In a mode item menu Manually saves an event in the data set. Press event button • Activate the NIBP function mode (press for < 2 s) Press the NIBP •...
  • Page 79 5 Operation If the timer has expired: The device automatically selects the Adult patient group. 2. During ongoing operation: Open the application menu with the navigation knob and change the patient group. When doing so, please note: The Infant patient group is not available in AED mode.

  • Page 80: Performing Defibrillation

    5 Operation 5.5 Performing defibrillation 5.5.1 Semi-automatic defibrillation in AED mode The defibrillation sequence in the AED mode described here corresponds to the device settings as delivered. The operator menu enables you to adapt the device to users’ qualification level and to provide optimal support to the latter during resuscitation measures whilst taking the regional features into account.
  • Page 81 5 Operation 1. Select AED mode with the AED function button. When doing so, please note: • Depending on the patient group selected, the AED settings from the operator menu which apply to this group are taken as the basis. •...
  • Page 82 5 Operation If you operate the device via the line power and the inserted battery is defective or if the battery does not have sufficient capacity to charge the capacitor for shock energy in AED mode, the device guides you through cardiopulmonary resuscitation without creating a shock standby.
  • Page 83 5 Operation Risk of injury from electric shock! The electric shock administered to the patient may result in injury to the patient, user or bystanders. ⇒ Stand clear of the patient. ⇒ Keep patient away from liquids (e.g. blood, gel or saline solution).
  • Page 84 5 Operation Shock not required The device performs a cardiac rhythm analysis, charges for shock delivery and outputs the message: Voice prompt AED instruction Stand clear of the patient Stand clear of the patient Cardiac rhythm is being analyzed Analysis If, based on the cardiac rhythm analysis, the device determines that a shock is not required, the device outputs the message: Voice prompt...
  • Page 85 5 Operation After cardiac rhythm analysis and shock delivery (if necessary), the device instructs you to carry out cardiopulmonary resuscitation. A metronome provides a guide for chest compressions. Voice prompt (optional) AED instruction Carry out cardiopulmonary Cardiopulmonary resuscitation resuscitation 1. Perform chest compressions: •...
  • Page 86 5 Operation 5.5.2 Manual defibrillation (only with Manual defibrillation option) This function is only available if it has been enabled and activated by the operator: Operator menu | System settings | Enable options | Manual mode (see "8.8 System settings", page 137).
  • Page 87 5 Operation Risk of injury due to incorrectly selected patient group! If the wrong patient group is selected, the shock energy may be insufficient or too high for the selected patient group and can injure the patient. ⇒ Adapt the patient group to the patient. ⇒...
  • Page 88 5 Operation Risk of injury from electric shock! The electric shock administered to the patient may result in injury to the patient, user or bystanders. ⇒ Stand clear of the patient. ⇒ Keep patient away from liquids (e.g. blood, gel or saline solution).

  • Page 89: Performing Pulse Oximetry Monitoring

    5 Operation 5.6 Performing pulse oximetry monitoring Requirement • The device is switched on (see "5.1 Switching the device on", page 76). • A patient group is selected (see "5.4 Selecting the patient group", page 78). • A pulse oximetry sensor is connected (see "4.5 Connecting the pulse oximetry sensor", page 60).

  • Page 90: Performing Ecg Monitoring

    5 Operation In the curve view: Evaluate the SpO curve (Pleth) and read off the measured values for arterial oxygen saturation (SpO ) and pulse rate (Pulse). 5. If necessary: Make the following SpO settings in the user menu (see "7.3.3 SpO settings", page 114): •...
  • Page 91 5 Operation 3. If necessary: Open the application menu with the navigation knob and change the device volume. 4. If necessary: Switch between parameter view and curve view with the view button 5. Evaluate the ECG leads and heart rate. 6.

  • Page 92: Performing Non-Invasive Blood Pressure Measurement (Nibp)

    5 Operation Set automatic alarm limits in the application menu (see "6 Application menu", page 106). 8. If necessary: Switch off the heart rate tone/pulse tone with the function button The symbol appears. 9. If necessary: Open the application menu with the navigation knob and change the device volume.
  • Page 93 5 Operation • Patient position (ideal position: Sitting comfortably, legs not crossed, feet flat on the floor, back and arm supported, middle of the NIBP cuff level with the right heart atrium) • Exertion (recommendation: Patient should rest for 5 minutes before the measurement, keep still during the measurement and not speak) •...
  • Page 94 5 Operation 3. If necessary: Adapt the initial NIBP cuff pressure to the patient with the Initial function button and navigation knob. When doing so, please note: Following successful NIBP measurement, the initial NIBP cuff pressure adapts to the patient (approx. 30 mmHg above the systolic measured value of the previous NIBP measurement).
  • Page 95 5 Operation 8. If necessary: Set alarm limits in the user menu (see "7.3.1 Alarm settings", page 111). Set automatic alarm limits in the application menu (see "6 Application menu", page 106). 9. If necessary: Press the Back function button. Press the NIBP button for <...
  • Page 96 5 Operation 5. Press the Start function button. Press the NIBP button for < 2 s. An NIBP measurement starts. At the end of the measurement, the device shows the systolic and diastolic arterial pressure, the timer expires and the next measurement starts automatically. 6.

  • Page 97: Using The Audio Alarm Output

    5 Operation Performing venous stasis Requirement • An NIBP cuff is connected to the NIBP connecting tube (see "4.7 Attaching the NIBP cuff", page 68). • The device is switched on (see "5.1 Switching the device on", page 76). • The Adult patient group is set.

  • Page 98: Saving The Event Manually In The Session Data Set

    5 Operation Result The audio alarm output is canceled for this alarm. The symbol appears on the display and no audio signal is output for this alarm. 5.9.2 Pausing/muting the audio alarm output Requirement An alarm is active and is audible. 1.

  • Page 99: Reprocessing The Device After Use

    5 Operation Requirement • The device is switched on (see "5.1 Switching the device on", page 76). • The patient group is set (see "5.4 Selecting the patient group", page 78). 1. Press event button Result The device saves an event with the designation Manual event in the session data set and an acknowledgment tone is heard.

  • Page 100: Saving Session Data/Status Log

    5 Operation 5.12 Saving session data/status log The device always saves the session data and status log to its internal memory. The status log is required in order to be able to analyze the data should servicing be necessary. If an SD card is inserted in the SD card slot, the device automatically saves the data to the SD card in addition.

  • Page 101: Analyzing Sessions

    5 Operation Result The session data/status log are located on the SD card. 5.13 Analyzing sessions You can analyze and archive device session data using the DEFIview WM 45120 PC software. 1. Remove the SD card (see "4.8.2 Removing the SD card", page 74).

  • Page 102: Transferring The Device Configuration To Another Device

    5 Operation 5.15 Transferring the device configuration to another device Using the device’s SD card, you can transfer settings saved in the operator menu to another device. Risk of injury from different alarm presets in the same or similar devices! Different alarm presets in the same or similar devices in different application areas can confuse the user and result in injury to the patient.

  • Page 103: Updating The Software

    1. If necessary: Download the current software from the Login area of the WEINMANN Emergency website to the SD card. 2. If the software is available as a ZIP file: Unzip the software. 3. Place the file in the SD card’s root directory. When doing so, please note: The file must not be in a sub-folder.
  • Page 104 5 Operation 7. Select new software with the navigation knob. Damage to the device caused by moving the device and/or pressing buttons during the update! Moving the device and/or pressing buttons during the update may cancel the update and damage the device. ⇒...
  • Page 105 5 Operation 13. Press and hold the On/Off button for at least 2 seconds to switch off the device and save the settings. 14. Perform a function check (see "10.2 Performing a function check", page 148). 15. If necessary: Set the date and time (see "8.8 System settings", page 137).

  • Page 106: Application Menu

    6 Application menu Application menu The application menu contains functions and settings which can be accessed quickly and easily during use. 6.1 Navigating the application menu Requirement • The device is switched on (see "5.1 Switching the device on", page 76).

  • Page 107: Menu Structure

    6 Application menu 6.2 Menu structure ! Infant   ! Child for adults !       6-1 Application menu MEDUCORE Standard...

  • Page 108: Settings

    6 Application menu 6.3 Settings Possible Parameter Description Factory setting values 25 % 50 % Here you can set the volume of the device for Volume 75 % 75 % the current session. 100 % for adults Child For adults Patient group Here you can select the patient group.

  • Page 109: User Menu

    7 User menu User menu The user menu contains functions and settings which influence the current session and which are not saved permanently as device presets. If the device was switched off for < 30 s and, if whilst switched on previously, patient measurements were taken or a manual event was saved, the settings made previously in the user menu are retained.

  • Page 110: Menu Structure

    7 User menu 7.2 Menu structure Alarm limit settings    Heart rate ↑ Autom. alarm limits Heart rate ↓ Pulse rate ↑ Amplitude scaling Pulse rate ↓   Speed saturation ↑ Line filter saturation ↓ NIBP systolic ↑ NIBP systolic ↓...

  • Page 111: Settings

    7 User menu 7.3 Settings 7.3.1 Alarm settings Risk of injury due to alarm limits which are too high or too low! Alarm limits which are either too high or too low can prevent the device from emitting an alarm, thereby putting the patient at risk. ⇒...
  • Page 112 7 User menu Factory setting for patient Possible group Parameter Description values Adult Child Infant 35/min-250/min, Heart rate 120/min 150/min 200/min in increments of 5 Here you can set the 30/min-245/min, upper ( ) and lower Heart rate 50/min 50/min 100/min in increments of 5 ( ) limits as of which...
  • Page 113 7 User menu 7.3.2 ECG settings 7-3 ECG settings sub-menu Parameter Possible values Description Factory setting Here you can set the strength of the ECG signal and thus the height of auto the ECG curve. 2 mm/mV If the auto setting has been Amplitude scaling 5 mm/mV selected, the strength of the ECG...
  • Page 114 7 User menu 7.3.3 SpO settings 7-4 SpO settings sub-menu Parameter Possible values Description Factory setting 12.5 mm/s Here you can set the speed of the Speed 25 mm/s curve display and thus change 25 mm/s 50 mm/s the temporal resolution. Activated Here you can set whether the pulse tone should take priority over the...
  • Page 115 7 User menu 7.3.4 System settings 7-5 System settings sub-menu Possible Factory Parameter Description values setting 10 %-100 %, in Here you can set the display Brightness 70 % 10 % increments brightness. Year Here you can set the date and time.

  • Page 116: Operator Menu

    8 Operator menu Operator menu Risk of injury due to incorrectly set parameters or too few/too many enabled functions in the operator menu! Incorrectly set parameters or too few/too many enabled functions in the operator menu can result in incorrect settings in the user menu or too limited/too comprehensive device functions.

  • Page 117: Navigating The Operator Menu

    2. Select access code with the navigation knob and confirm. The operator menu is protected by an access code. Upon delivery this code is 0000. WEINMANN Emergency recommends changing this code as soon as the device is put into operation.

  • Page 118: Aed Settings

    8 Operator menu 8.2 AED settings You can make presets for the AED mode in the AED setup menu. The factory settings are such that the ERC guidelines for resuscitation are met. Adjustments to the AED settings can result in users no longer being supported in compliance with these guidelines.
  • Page 119 8 Operator menu 8.2.1 Menu structure   AED settings for adults AED settings First shock    Child Energy curve Further shocks Pictograms in parameter view Duration !  Ventilation pause Charging during   CPR phase analysis CV ratio Start in intub.
  • Page 120 8 Operator menu Possible Factory Parameter Description values setting Adult AED settings/child AED settings Here you can set the time interval for ventilation between the chest compressions. When choosing a setting, consider whether the voice prompt is deactivated: • When the voice prompt is activated, the pause 3 s to begins after the last...
  • Page 121 8 Operator menu Possible Factory Parameter Description values setting Adult AED settings/child AED settings Here you can set whether the Activated voice prompts for guiding chest compression (Ventilate CPR voice twice and Carry out Deactivated prompts Deactivated cardiopulmonary resuscitation) should be output.

  • Page 122: Alarm Settings

    8 Operator menu 8.3 Alarm settings Risk of injury due to alarm limits which are too high or too low! Alarm limits which are either too high or too low can prevent the device from emitting an alarm, thereby putting the patient at risk. ⇒...
  • Page 123 8 Operator menu 8-2 Alarm settings sub-menu 8.3.1 Menu structure      Alarm limit settings for adults !  Alarm limit   settings for children Alarm limit settings for infants   Pause audio Reminder signal    VF/VT alarm selectable VF/VT alarm...
  • Page 124 8 Operator menu 8.3.2 Possible values Possible Factory Parameter Description values setting 35/min-250/min, Heart rate 120/min in increments of 5 30/min-245/min, Heart rate 50/min Here you can set the upper in increments of 5 ( ) and lower ( ) limits for 35/min-250/min, the patient group as of which Pulse rate...
  • Page 125 8 Operator menu Possible Factory Parameter Description values setting 35/min-250/min, Heart rate 150/min in increments of 5 30/min-245/min, Heart rate 50/min Here you can set the upper in increments of 5 ( ) and lower ( ) limits for 35/min-250/min, the patient group as of which Pulse rate 150/min...
  • Page 126 8 Operator menu Possible Factory Parameter Description values setting 35/min-250/min, Heart rate 200/min in increments of 5 30/min-245/min, Heart rate 100/min Here you can set the upper in increments of 5 ( ) and lower ( ) limits for 35/min-250/min, the patient group as of which Pulse rate 200/min...
  • Page 127 8 Operator menu Possible Factory Parameter Description values setting Here you can set the interval at which a reminder signal 1 min Reminder signal reminds you that the audio 2 min 2 min alarm output is paused or 5 min muted.

  • Page 128: Manual Mode Settings (Only With Manual Mode Option)

    8 Operator menu 8.4 Manual mode settings (only with Manual mode option) You can make the presets for the defibrillation energies in the manual mode setup menu. The factory settings are such that the ERC guidelines for resuscitation are met. Adjustments to the settings for the manual mode can result in users no longer being supported in compliance with these guidelines.
  • Page 129 8 Operator menu 8.4.1 Menu structure      for adults !  Child   Infant         #    "   8.4.2 Possible values Possible Factory Parameter Description values...

  • Page 130: Ecg Settings

    8 Operator menu 8.5 ECG settings In the ECG setup menu, you can make the presets for displaying the ECG curves. 8-4 ECG settings sub-menu MEDUCORE Standard...
  • Page 131 8 Operator menu 8.5.1 Menu structure      !    Amplitude scaling   Speed Line filter       #    "   8.5.2 Possible values Possible Parameter Description Factory setting...

  • Page 132: Spo 2 Settings

    8 Operator menu 8.6 SpO settings In the SpO setup menu you can make the presets for displaying the plethysmogram and for outputting the pulse tone. 8-5 SpO settings sub-menu MEDUCORE Standard...
  • Page 133 8 Operator menu 8.6.1 Menu structure      !      Speed    Pulse tone priority    #    "   8.6.2 Possible values Parameter Possible values Description Factory setting 12.5 mm/s...

  • Page 134: Nibp Settings

    8 Operator menu 8.7 NIBP settings In the NIBP setup menu you can make the presets for blood pressure measurement and the venous stasis function. You can adapt the device to the patient group using the specific NIBP settings. 8-6 NIBP settings sub-menu MEDUCORE Standard...
  • Page 135 8 Operator menu 8.7.1 Menu structure      !      for adults    Child Initial cuff pressure Infant Interval    iv cuff pressure iv duration #    "   8.7.2 Possible values Possible...
  • Page 136 8 Operator menu Possible Factory Parameter Description values setting 0:30 min 0:45 min 1:00 min 1:15 min 1:30 min Here you can set after how 1:45 min long another NIBP Interval 2:00 min measurement is to be started 3:00 min automatically.

  • Page 137: System Settings

    8 Operator menu 8.8 System settings In the System setup menu, you can make the presets for the system and also perform functions which are conceived exclusively for the device operator. 8-7 System settings sub-menu MEDUCORE Standard...
  • Page 138 8 Operator menu 8.8.1 Menu structure Start mode   Start view Brightness Display Night colors Volume    Language Regional settings Line frequency ! Enter enable code    Enable options Manual mode* Operator menu   Manual mode* Curve view Disable functions...
  • Page 139 8 Operator menu 8.8.2 Possible values Possible Factory Parameter Description values setting Monitor Here you can set in which Start mode Monitor mode the device is to start. Manual Curves Here you can set in which Start view Curves Parameter view the device is to start.
  • Page 140 8 Operator menu Possible Factory Parameter Description values setting Here you can disable certain functions and protect against unauthorized access with a code prompt: • Manual mode • Curve view* • Venous stasis Disable functions Each function can be protected individually and also assigned an individual code.
  • Page 141 8 Operator menu *If you disable curve view but this is set as start view, the device switches on without requesting a code. The request for a code only appears when you switch to parameter view and back to curve view.

  • Page 142: Device Information

    8 Operator menu 8.9 Device information You will find information on the device and the battery in the device information menu. 8.9.1 Menu structure      !            #    Device information "  ...
  • Page 143 8 Operator menu 8.9.2 Information displayed Parameter Description Serial number: Here you can find out the device serial number. This is located on the device information label. Device ID: Here you can find out the device ID. This is required to procure optional functions Passed function check: Here you can find out when the last successful function check was performed.

  • Page 144: Hygienic Reprocessing

    Always carry out a function check after the hygienic reprocessing (see "10.2 Performing a function check", page 148). • You can find further information about hygienic reprocessing and a list of all the suitable cleaning agents and disinfectants in a brochure on our website at www.weinmann-emergency.com. MEDUCORE Standard...

  • Page 145: Intervals

    9 Hygienic reprocessing 9.2 Intervals Wipe disinfection After each use At least 1x weekly Device Reusable components x Reusable accessories Short-term NIBP cuffs 9.3 Hygienic reprocessing of the device Damage to the device caused by ingress of liquids! The device is protected from water jets in line with IP55. Ingress of liquids may damage the device, components and accessories.
  • Page 146 9 Hygienic reprocessing 7. Carry out hygienic reprocessing of the device, components, and accessories as specified in the table below: Thermal Part Cleaning Disinfection Sterilization disinfection Device Battery Wipe with a damp Wipe disinfection cloth: Use water or (Recommendation: Not permitted Not permitted Power supply unit and ®...
  • Page 147 9 Hygienic reprocessing 8. Connect the following parts to the device: • Trunk cable with defibrillation electrodes • Pulse oximetry sensor connecting cable with pulse oximetry sensor • ECG cable • NIBP connecting tube with NIBP cuff 9. Insert battery. 10.

  • Page 148: Function Check

    10 Function check 10 Function check After being switched on, the device performs an automatic function check which serves to check the functionality of all the key functions. The device also offers a step-by-step guide to performing a function check (see "10.2 Performing a function check", page 148).
  • Page 149 10 Function check • Defibrillation electrode packaging • ECG electrode packaging • ECG cable • Pulse oximetry sensor connecting cable • Pulse oximetry sensor • NIBP connecting tube • NIBP cuff 2. If necessary: Replace parts. 3. Check the expiry date on the ECG electrodes and defibrillation electrodes.
  • Page 150 10 Function check 7. Once all components are marked with a green checkmark: Press the Start function button. The function check starts and the shock administration test begins. The function check can now no longer be canceled. 8. Press the Charging function button. The shock capacitor is charged to 30 J and the energy is maintained for 30 seconds.
  • Page 151 10 Function check 9. If the shock energy capacitor is fully charged and the shock button flashes: Press shock button 10. Alarm system test: • If an audible alarm is output: Press the Yes function button. • If the alarm LED lights up red: Press the Yes function button. 11.
  • Page 152 10 Function check 12. If a part of the alarm system does not function: Press the No function button. 13. In the key function check, press all of the controls one after the other except for the On/Off button 14. If necessary: Press the menu button twice to cancel the key function check.

  • Page 153: Checking The Ecg Cables

    Result The function check is complete. 10.3 Checking the ECG cables In addition to visual inspection of the ECG cables, WEINMANN Emergency recommends checking function at regular intervals (see "10.2 Performing a function check", page 148): 1. Connect the ECG simulator to the ECG cable connection using the ECG cable.
  • Page 154 10 Function check In principle, any ECG simulator can be used. WEINMANN Emergency recommends the ECG simulator WM 45444. Alternatively, the ECG cable can be tested on a voluntary test person. 2. Switch on the ECG simulator and set a sinus rhythm.

  • Page 155: Checking The Nibp Cuff And Nibp Connecting Tube

    10 Function check 10.4 Checking the NIBP cuff and NIBP connecting tube In addition to the visual inspection of the NIBP cuff and NIBP connecting tube, WEINMANN Emergency recommends checking function at regular intervals (see "10.2 Performing a function check", page...

  • Page 156: Alarms And Faults

    11 Alarms and faults 11 Alarms and faults 11.1 General instructions The device emits an alarm as long as the cause continues to exist. Once the cause of the alarm no longer exists, the device no longer emits the alarm. This does not apply to NIBP measurement alarms or the battery operation alarm.
  • Page 157 11 Alarms and faults 11-1 Alarm line with VF/VT alarm (example) The device displays alarms as follows: • As text in the alarm line on the display • As audio alarm tones (via the loudspeaker) • With the alarm light (in the top right-hand corner on the front of the device) Alarms are emitted according to their priority: Type of alarm...

  • Page 158: Alarm Messages

    11 Alarms and faults Type of alarm Medium High priority Low priority signal priority Alarm light Color Frequency 2 Hz Not applicable Not applicable Duty cycle 33 % on Not applicable Not applicable Size 10 mm x 35 mm The device additionally displays physiological alarms through the flashing of the respective parameter field.
  • Page 159 11 Alarms and faults Alarm Cause Remedy Proceed according to the latest resuscitation guidelines. Asystole Asystole detected. If medically indicated, perform suitable treatment. Internal defibrillation module Defibrillation module defective Have the device repaired. defective. • Switch device off and back on Temporary device malfunction.
  • Page 160 11 Alarms and faults Alarm Cause Remedy If medically indicated, perform Measured diastolic blood pressure NIBP diastolic suitable treatment or adapt the is below the set lower alarm limit. alarm limits (see 7.3.1, p. 111). Re-enter presets in the operator Settings had to be reset to factory Settings lost menu.
  • Page 161 11 Alarms and faults Alarm Cause Remedy The pressure in the NIBP cuff was Check which influences resulted in increased to such a degree by the increase of excess pressure and Excessive NIBP cuff pressure external influences that the safety remedy these before the next valve opened.
  • Page 162 11 Alarms and faults Alarm Cause Remedy Pad connector of the defibrillation electrodes not connected or not Connect the pad connector of the Plug in pad connector correctly connected to the trunk defibrillation electrodes correctly (Monitor mode) cable, or trunk cable not to the trunk cable, or connect the connected or not correctly trunk cable correctly to the device.
  • Page 163 11 Alarms and faults 11.2.3 Low-priority alarm (turquoise) Alarm Cause Remedy Line power too low. Disconnect the line power supply Alarm goes off automatically after Battery operation by removing from the wall 10 s. Restore line power. mounting. Power outage Battery not inserted or incorrectly Insert battery correctly (see 4.2, p.
  • Page 164 11 Alarms and faults Alarm Cause Remedy Pulse oximetry sensor not attached Attach pulse oximetry sensor to Check seating of SpO sensor or not correctly attached to the the patient correctly (see 4.5, p. patient. 60). Attach pulse oximetry sensor to the patient correctly (see 4.5, p.

  • Page 165: Faults

    If you are not able to clear an error message with the aid of the table, you should contact the manufacturer WEINMANN Emergency or your authorized dealer to have the device repaired. To avoid more serious damage, do not continue using the device.
  • Page 166 11 Alarms and faults Fault Cause Remedy Device failure • Alarm LED flashes Device defective. Have the device repaired. • Audio alarm output 11.3.2 Defibrillation Fault Cause Remedy Attach defibrillation electrodes to the patient correctly (see 4.4, p. 57). Defibrillation electrodes incorrectly Connect pad connector of the The Check pad electrodes attached to the patient or pad...
  • Page 167 11 Alarms and faults Fault Cause Remedy Charge battery within permitted Battery temperature < 0 °C or temperature range (see 15.3, p. Battery not charging although it is > 45 °C. 178). not full Battery defective. Replace battery. 11.3.4 6-lead ECG Fault Cause Remedy...
  • Page 168 11 Alarms and faults Fault Cause Remedy Device incorrectly detects pulse Have the device repaired. The pulse oximetry sensor is not oximetry sensor as connected. connected to the device but the The alarm is only emitted if an sensor alarm does Plug in SpO signal has been successfully not appear...
  • Page 169 11 Alarms and faults 11.3.6 Non-invasive blood pressure (NIBP) monitoring Fault Cause Remedy NIBP cuff attached incorrectly. Reattach NIBP cuff (see 4.7, p. 68). NIBP cuff leaky. Replace NIBP cuff. Unsuitable patient position. Reposition the patient. Implausible measured values NIBP module defective. Have the device repaired.

  • Page 170: Maintenance

    12 Maintenance 12 Maintenance 12.1 General instructions Maintenance, safety checks (Germany only), inspections, and repairs must only be carried out by the manufacturer or a technician specifically authorized by the manufacturer. 12.2 Intervals Part concerned Interval Maintenance by Maintenance-free Annual safety check recommended Manufacturer or a technician Device specifically authorized by the Metrological check every two years...

  • Page 171: Sending In Device

    (see "9.3 Hygienic reprocessing of the device", page 145). 3. Send in the device and, if necessary, components and accessories to WEINMANN Emergency or a technician specifically authorized by WEINMANN Emergency. If you send in parts that are obviously contaminated,...

  • Page 172: Storage

    13 Storage 13 Storage 13.1 General instructions • When storing between sessions, observe the ambient conditions for continuous operation (see "15 Technical data", page 175). • During extended storage periods, observe the ambient conditions for storage (see "15 Technical data", page 175).

  • Page 173: Storing The Battery

    13 Storage 13.3 Storing the battery Requirement • The device and the battery have been cleaned and disinfected (see "9.3 Hygienic reprocessing of the device", page 145). • The battery is fully charged. • If available: The replacement battery is fully charged. 1.

  • Page 174: Disposal

    Pulse oximetry sensor • ECG cable • ECG electrodes • Power supply unit and charger • Function test resistor 14.2 Battery Do not dispose of used batteries in the household waste. Contact WEINMANN Emergency or a public waste disposal authority. MEDUCORE Standard...

  • Page 175: Technical Data

    15 Technical data 15 Technical data 15.1 Device The technical data of components and accessories may deviate. You should also note the sections which follow, as well as the Instructions for Use for the component/accessory part. Specification Device Product class according to Directive 93/42/EEC Dimensions (W x H x D) 242 mm x 137 mm x 130 mm...
  • Page 176 Resistance to falling Electromagnetic compatibility (EMC) as Test parameters and limit values can be requested from the per EN 60601-1-2: manufacturer WEINMANN Emergency if required. Radio interference suppression EN 55011 Radio interference immunity EN 61000-4 (parts 2 to 6, 8, and 11)

  • Page 177: Defibrillation Electrodes

    15 Technical data Specification Device Secured in rescue vehicle, aeroplane and helicopter as well as Type of rescue vehicle portable at the site of the emergency) EN 60601-1 EN 60601-1-2 EN 60601-1-6 EN 60601-1-8 EN 60601-1-12 EN 60601-2-4 Standards used EN 60601-2-27 EN 60601-2-49 EN 80601-2-30...

  • Page 178: Battery

    15 Technical data 15.3 Battery Specification Battery Type Li-ion Dimensions (W x H x D) 97 mm x 127 mm x 33 mm Weight 450 g Shock capacity (at 20 °C with new and fully charged 350 shocks at 200 J battery) Monitoring capacity Approx.

  • Page 179: Cardiobiphasic Defibrillation System

    15 Technical data 15.5 CARDIObiphasic defibrillation system Specification Defibrillation system Semi-automatic (AED mode) Operating mode Manual (Manual mode) Shock form Biphasic, current-limited, impedance-compensated Patient impedance: Max. 200 Ω Min. 5 Ω Adjustable: Energy curve: Shock sequence First shock: 1 J to 200 J Further shocks: 1 J to 200 J Analysis time 8 s under typical conditions...

  • Page 180: Ecg Monitoring System

    15 Technical data 15.6 ECG monitoring system Specification ECG monitoring system Max. patient impedance with 6-lead ECG 500 kΩ Detected heart rate (with ECG derivation via ECG 30 bpm to 250 bpm cable or derivation via defibrillation electrodes) Suitability for direct use on the heart Type CF (6-lead ECG) Displayed heart rates with pacemaker impulses (with If pacemaker impulses are detected, "---"...

  • Page 181: Ecg Analysis System Cardiologic

    15 Technical data 15.7 ECG analysis system CARDIOlogic Specification ECG analysis system Duration of analysis in the AED mode: 8 s under typical conditions Analysis time (VF/VT) Duration of analysis VF/VT alarm: 8 s with continuous measurement ECG derivation used for Lead II of the pad electrodes is primarily used for analysis.

  • Page 182: Pulse Oximetry Monitoring

    15 Technical data A = Number of correct positive decisions B = Number of false positive decisions C = Number of false negative decisions D = Number of correct negative decisions This results in the following values: Formula for the Calculation Result calculation...

  • Page 183: Non-Invasive Blood Pressure (Nibp) Monitoring

    15 Technical data Specification Pulse oximetry Reference methods for determining the accuracy of Oxitest simulator testing the pulse rate Wavelength with maximum intensity 660 nm/890 nm (2.5 to 4.5 mW) Curve form Normalized 8 s (It can take up to 16 s for the correct SpO value Update rate of SpO mean...

  • Page 184: Operation/Data Management

    15 Technical data 15.10 Operation/data management Specification Operation/data management Light symbols Display Device status indicators Voice prompts Audio outputs Alarm tones Signal tones Automatic recording of ECG, SpO and NIBP Session documentation measurement values and event data Data transfer Via SD card: SD card with 32 GB Data evaluation Via DEFIview PC software 15.11 Alarm delay times...

  • Page 185: Saving Of Session Data

    15 Technical data Alarm Delay time saturation 10.0 s signal quality 10.0 s VF/VT Patient is connected with this condition 11.3 s Patient already connected 5.3 s 15.12 Saving of session data Hours of memory with typical use with 6-lead ECG, SpO measurement and NIBP measurement) Internal device memory (100 MB)* 1675...
  • Page 186 15 Technical data Delay in treatment due to power supply network faults! Transient or pulsed conducted interference may cause artifacts in the ECG signal and thus interfere with device functioning and delay treatment. ⇒ If there is major interference in the power supply network, only operate the device with a battery.

  • Page 187: The Cardiobiphasic Shock Impulse

    0.66 0.15 0.38 Further technical data can be requested from the manufacturer WEINMANN Emergency. 15.14 The CARDIObiphasic shock impulse A characteristic of the CARDIObiphasic shock impulse is that it limits the maximum current. This greatly reduces the risk of myocardial damage, which is mainly caused by electric currents that are too high, especially where patient impedance is low.
  • Page 188 15 Technical data The mean ratio of delivered electric charge between the second (negative) and the first (positive) phase is 0.38. For safety reasons, voltages of no higher than 2000 V are used. The resulting currents as a function of patient impedance are shown in the following graph by way of example.
  • Page 189 15 Technical data Delivered energy as a function of patient impedance* Precision Selected Patient impedance in Ω energy in J delivered energy ±3 J ±3 J 10.8 13.2 11.6 10.2 ±3 J 15.7 20.4 18.4 16.5 15.3 13.6 12.4 ±3 J 10.2 19.9 25.6...

  • Page 190: Scope Of Supply

    16 Scope of supply 16 Scope of supply 16.1 Standard product MEDUCORE Standard WM 45300 Article Article number MEDUCORE Standard , basic device WM 45310 Battery WM 45045 Trunk cable WM 45397 Defibrillation electrodes for adults WM 45418 ® SoftTip pulse oximetry sensor, size M, reusable WM 45432 Pulse oximetry sensor connecting cable...

  • Page 191: Accessories

    16 Scope of supply 16.3 Accessories Accessories can be ordered separately, if required. Article Article number Power supply Charging station for battery WM 45045 WM 45190 Power supply unit/charger, 100 W, including power cord WM 28937 WM 17465 Adapter MAG for charging with power supply unit/charger or WM 28979 12 V adapter cable Adapter cable 12 V vehicle electrical system/ODU connector...
  • Page 192 16 Scope of supply Article Article number NIBP cuff, small adult, for 17-25 cm upper arm circumference, WM 45462 reusable NIBP cuff, adult, for 23-33 cm upper arm circumference, WM 45463 reusable NIBP cuff, adult plus, for 28-40 cm upper arm circumference, WM 45464 reusable NIBP cuff, large adult plus, for 40-55 cm upper arm...

  • Page 193: Replacement Parts

    17 Appendix 17.1 Warranty Starting from the date of purchase, WEINMANN Emergency offers the customer a limited manufacturer’s warranty on a new original WEINMANN Emergency product or replacement parts installed by WEINMANN Emergency in accordance with applicable warranty terms and conditions for the particular product and the warranty periods listed below.

  • Page 194: Declaration Of Conformity

    17 Appendix 17.2 Declaration of conformity WEINMANN Emergency Medical Technology GmbH + Co. KG declares herewith that the product complies fully with the respective regulations of the Medical Device Directive 93/42/EEC. The unabridged text of the Declaration of Conformity can be found on our website at www.weinmann-emergency.com.
  • Page 196 Manufacturer Center for Production, Logistics, Service WEINMANN Emergency WEINMANN Emergency Medical Technology GmbH + Co. KG Medical Technology GmbH + Co. KG Frohbösestraße 12 Siebenstücken 14 22525 Hamburg 24558 Henstedt-Ulzburg GERMANY GERMANY T: +49 40 88 18 96-120 E: customerservice@weinmann-emt.de...

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