ARGUS PRO LifeCare 2 Service Manual Rev b Nov 2012

Sales and Service Information The SCHILLER sales and service centre network is world-wide. For the address of your local distributor, contact your nearest SCHILLER subsidiary. In case of difficulty, you can find a complete list of all distributors and subsidiaries on our Internet site: http://www.schiller.ch Sales information can also be obtained from: [email protected]

Address Headquarters SCHILLER AG Altgasse 68 CH-6341 Baar, Switzerland Web:

Phone: +41 (0) 41 766 42 42 Fax: +41 (0) 41 761 08 80 E-mail: [email protected] www.schiller.ch

ARGUS PRO LifeCare 2 bears the CE-0123 mark (Notified Body TÜV-SÜD Produkte Service GmbH, Ridlerstr. 65, 80339 Munich, Germany), indicating its compliance with the essential requirements of the Annex I of the Medical Device Directive 93/42/EE regarding safety, functionality and labelling. The requirements apply to patients, users and third persons who come into contact with this device within the scope of its intended use.

Article no.: 2.540060 Rev.: b Issue date: 21.11.12

ARGUS PRO LifeCare 2

Service Handbook

Contents 1

Safety Notes ... 7

1.1

Responsibility of the User ... 7

1.2

Organisational Measures ... 7

1.3

Intended use ... 7

1.4

Safety-Conscious Operation ... 7

1.5

Safety Facilities ... 8

1.6

Operation with other Devices ... 8

1.7

Networks and Internet ... 8

1.8

Maintenance... 9

1.9

Safety Symbols and Pictograms ... 10

1.9.1 1.9.2 1.9.3 1.9.4

Symbols used in this document ... 10 Symbols used on the device and on the battery ... 11 Symbols used on the electrode package ... 12 Symbols used on the SpO2 sensor packaging ... 12

1.10

Additional Terms ... 13

Art. no.: 2.540060 Rev.: b

1.10.1 Terms of Warranty ... 13

2

Components and Operation ... 14

2.1

Design... 14

2.2

Options ... 15

2.3

Operating Elements... 16

2.3.1 2.3.2 2.3.3 2.3.4 2.3.5 2.3.6

Front... 16 Connections ... 17 Description of keys... 18 Operating elements paddles ... 19 LED indicators... 19 Display ... 20

2.4

Wall Mounting ... 21

2.4.1 2.4.2

Certifications ... 21 Connecting to an external direct-current source ... 23

2.5

SCHILLER Charging Unit CS-1... 27

2.5.1 2.5.2 2.5.3 2.5.4 2.5.5 2.5.6 2.5.7 2.5.8

Battery Charging Options... 27 Inserting a battery ... 27 Control Panel ... 28 Battery Calibration... 29 Input and Output Supplies... 30 Installation ... 31 Positioning... 32 Wall Mounting ... 33

3

Initial Operation ... 34

3.1

Mains and Battery Operation... 34

3.1.1 3.1.2 3.1.3

Connecting the unit to the mains and switching it on ... 34 Battery operation... 35 Operation with external direct-current source ... 36

3.2

Switching off and Disconnecting from Mains... 37

3.2.1 3.2.2

Isolating the device from the mains supply ... 37 Internal safety discharge ... 37

Page 1

ARGUS PRO LifeCare 2

Page 2

Inserting Printing Paper ... 38

3.3.1

Operation of the docking station ... 38

3.4

Ensuring operational readiness ... 39

3.4.1

Mains supply interruption ... 39

3.5

Operation... 40

3.5.1 3.5.2

Direct menu access ... 40 Menu access via measurement field... 41

3.6

Programming Display Configurations ... 42

3.7

Alarm Messages ... 43

3.7.1

Alarm list ... 44

3.8

Alarm Limit Settings... 45

3.9

Patient Data ... 46

3.9.1 3.9.2

Patient data - entering... 46 Save patient data ... 46

3.10

System and Technical Messages... 47

3.10.1 3.10.2 3.10.3 3.10.4 3.10.5 3.10.6 3.10.7

Accumulator ... 47 ECG ... 47 SpO2... 47 CO2... 48 Temperature ... 49 IBP ... 49 NIBP... 49

4

Default and User-Defined Alarm Limits 51

4.1

Settings Menu ... 52

4.1.1 4.1.2 4.1.3 4.1.4 4.1.5 4.1.6

Parameter ... 52 Curves... 54 Alarm... 54 Change layout... 54 Set sound... 54 Set brightness ... 54

4.2

Menu Patient ... 55

4.3

Alarm Limits ... 56

4.3.1

Operator 1 and 2 alarm limits... 56

4.4

Trend... 57

4.5

Communication (deleting the memory) ... 57

5

Device Configuration ...58

5.1

Alarm... 59

5.1.1

Defining the default alarm limits... 59

5.2

User Configuration ... 62

5.3

Service Configuration ... 64

5.4

Language Configuration ... 64

5.5

Factory Configuration ... 64

5.6

Device information ... 64

5.7

Download... 65

5.7.1 5.7.2

Download via USB ... 65 Download via Ethernet... 65

5.8

Physical Overview ... 66

5.8.1 5.8.2

Exploded view back ... 66 Mounting exploded view front ... 67

Art. no.: 2.540060 Rev.: b

3.3

ARGUS PRO LifeCare 2

Service Handbook

Art. no.: 2.540060 Rev.: b

5.8.3

Exploded View Thermo printer... 68

5.9

Measuring Principals and Theory ... 69

5.9.1 5.9.2 5.9.3 5.9.4 5.9.5 5.9.6 5.9.7 5.9.8 5.9.9

Measuring principle IRMA Mainstream CO2 Module ... 69 ECG ... 70 Connecting a 4- or 10-lead ECG patient cable ... 71 Connecting a 4-lead ECG patient cable... 71 Connecting a 10-lead ECG patient cable... 72 .NIBP Processing ... 73 Temperature... 75 Invasive blood pressure ... 76 SpO2 measuring ... 77

5.10

Functional Overview ... 79

5.10.1 5.10.2 5.10.3 5.10.4 5.10.5 5.10.6 5.10.7

System architecure ... 79 Power supply... 80 Connetction diagramm ... 81 Defibrillator Boards... 82 CPU Board DE 8-1... 82 Function of the Master Board PB8-1... 86 Function of the Parameter Board PB8-4 ... 86

5.11

Assembly and Disassembly ... 89

5.11.1 5.11.2 5.11.3 5.11.4 5.11.5 5.11.6 5.11.7 5.11.8 5.11.9

Safety Notes... 89 Opening the Case ... 89 Disassembly the parameter board ... 91 Disassembly the Defibrillator board ... 92 Disassembly of the connections panels ... 93 Disassembly the defi capacitor and battery board ... 93 Assembly defibriallor board... 94 Assembly Parameter board... 96 Assembly the Front Case... 97

6

ARGUS PRO LifeCare 2 Software ... 98

6.1

Overview... 98

6.1.1

Used tools ... 99

6.2

Download Host SW (USB)... 99

6.3

Parameter software download ... 100

6.3.1 6.3.2 6.3.3 6.3.4 6.3.5 6.3.6

Installation of the USB service adapter ... 100 Getting ready for software download ... 100 Initiate the ARGUS PRO LifeCare 2 and Download Software ... 101 Updating the Parameter (PB-1000) Software ... 102 NIBP tests ... 102 Troubleshooting ... 103

7

Measurement Checks ... 104

7.1

General information ... 104

7.1.1

Reference Documents ... 104

7.2

Measurement Checks... 105

7.2.1 7.2.2 7.2.3

General Test Equipment ... 105 Test Requirements... 106 Preliminaries ... 106

7.3

ECG... 107

7.3.1 7.3.2 7.3.3

Equipment Required ... 107 ECG printout reference test ... 107 Check ECG curve on the LCD with the reference printout ... 109

7.4

SpO2 ... 111

7.4.1

Equipment Required ... 111

Page 3

ARGUS PRO LifeCare 2

7.4.2

Procedure ... 111

7.5

NIBP ... 112

7.5.1 7.5.2 7.5.3 7.5.4 7.5.5 7.5.6 7.5.7

Test Setup and Preliminaries... 113 Getting ready for NIBD Test... 114 Cuff Over Pressure Test ... 115 Leak Rate and Cuff Pressure Tolerance Test... 116 Deflation Curve Test ... 117 Measurement confirmation with a Test Person... 118 Troubleshooting ... 118

7.6

Invasive Blood Pressure ... 119

7.6.1 7.6.2

Invasive BP with a test Box... 119 Invasive BP with a Manometer ... 120

7.7

Temperature ... 121

7.7.1 7.7.2 7.7.3 7.7.4 7.7.5

Equipment Required ... 121 Procedure ... 121 Temperature check of the sensor according German directive ... 122 Messung des Isolationswiderstand des Temperaturaufnehmer ... 122 Calculation of resistance and temperature ... 123

7.8 7.8.1 7.8.2 7.8.3 7.8.4

CO2 Zeroing/ Offset Calibration / ... 124 Zero reference calibration for the IRMA CO2 sensor... 124 O2 compensation... 124 Sensor LED indications... 125 etCO2 Measurement Check ... 126

7.9

Pacemaker... 127

7.9.1 7.9.2 7.9.3 7.9.4 7.9.5

Equipment Required ... 127 Test Setup for Pacemaker Energy Level and Timing Check ... 127 Timing and Pacemaker Delivery Check... 128 Pacemaker settings for Fix mode ... 128 Timing and Energy Level (Demand Mode) Check ... 129

7.10

Defibrillator... 131

Page 4

8

Maintenance ...137

8.1

Maintenance Interval ... 137

8.1.1

Maintenance Interval Table... 137

8.2

Functional test ... 139

8.2.1 8.2.2 8.2.3 8.2.4 8.2.5 8.2.6

Visual inspection of the device... 139 Battery charging status ... 139 Key test ... 139 Defibrillator test ... 140 Functional test - measurement values ... 141 Alarm tests ... 141

8.3

Maintenance Interval for the Batteries... 142

8.3.1 8.3.2 8.3.3

Charging and calibrating the battery ... 142 Battery disposal ... 142 Disposal at the end of the device's useful life ... 142

8.4

Cleaning the casing and cables ... 143

8.4.1 8.4.2 8.4.3

Approved cleaning solutions ... 143 Non-admissible detergents ... 143 Notes on the cleaning and disinfection ... 144

8.5

Disinfection ... 145

Art. no.: 2.540060 Rev.: b

7.10.1 Equipment Required ... 131 7.10.2 Setup... 131 7.10.3 Manual Mode Check ... 132 7.10.4 AED Mode Check ... 133 7.10.5 Defibrillator Energy Check ... 134

Service Handbook

8.5.1 8.5.2

Admissible disinfectants... 145 Non-admissible disinfectants ... 145

8.6

Cleaning the Thermal Print Head/Pressure Roller ... 145

8.7

Inspection and Check List Tables... 146

8.7.1 8.7.2 8.7.3 8.7.4 8.7.5

Weekly ... 147 At least every six months ... 148 Every 12 months ... 148 Every 24 months ... 148 Lifed-item replacement every 3 - 5 years... 149

8.8

Error Detection ... 150

8.8.1 8.8.2 8.8.3

General errors ... 150 Technical error messages... 151 Accessories and disposablesAccessories and disposables ... 152

9

Technical Data ... 154

9.1

System Data ... 154

9.2

Defibrillation pulse ... 156

9.3

Pacemaker... 158

9.4

Measured Values ... 159

9.4.1 9.4.2 9.4.3 9.4.4 9.4.5 9.4.6 9.4.7

ECG ... 159 Temperature... 160 NIBP – non-invasive blood pressure... 160 IBP - invasive blood pressure ... 160 SpO2 - Pulse oximetry ... 161 etCO2 - Capnography ... 162 Storage of an intervention (option)... 163

9.5

Literature ... 164

9.6

Glossary ... 164

9.7

EMC Information... 165

9.7.1 9.7.2 9.7.3

Electromagnetic emissions ... 165 Electromagnetic immunity ... 165 Recommended separation distances... 167

10

Test Protocol Forms ... 169

Art. no.: 2.540060 Rev.: b

ARGUS PRO LifeCare 2

Page 5

Art. no.: 2.540060 Rev.: b

ARGUS PRO LifeCare 2

Page 6

ARGUS PRO LifeCare 2

Service Handbook

Safety Notes Responsibility of the User

1 1.1

1 Safety Notes This Service Handbook is for qualified service personnel only, trained by Schiller AG. Refer to the operating instruction manual 2.510846 for operation the device.

1.1

Responsibility of the User V Specify the competencies of the personnel for operation and repair. V Ensure that service personnel have read and understood these service instructions. In particular this section “safety notes" must be read and understood. V Have damaged or missing components replaced immediately. V The service personnel is responsible for compliance with all applicable accident prevention regulations and safety regulations.

1.2

Organisational Measures V Before servicing the unit, ensure that an introduction regarding the unit functions and the safety precautions has been provided by Schiller AG V Keep these service instructions in an accessible place for reference when required. Make sure that they are always complete and legible. V Observe the operating instructions and service instructions. V These service instructions do not override any statutory or local regulations, or procedures for the prevention of accidents and environmental protection.

1.3

Intended use V See operating instruction of the APLC 2.

Art. no.: 2.540060 Rev.: b

1.4

Safety-Conscious Operation V Do not place any liquids on the unit. If liquid should be spilled over the device, immediately disconnect the device from the mains and wipe it. The device must be serviced before reusing. V Danger of electric shock! Do not open the device without disconnecting the device from the mains. V Before cleaning and to isolate the mains power supply, switch the unit off and disconnect it from the mains by removing the plug. V Do not use high temperature sterilisation processes (such as autoclaving). Do not use E-beam or gamma radiation sterilisation. V Do not use solvent or abrasive cleaners on either the unit or cable assemblies. V Do not, under any circumstances, immerse the unit or cable assemblies in liquid V As soon as the GSM module is switched on, all persons must keep a distance of at least 20 cm from the sending antenna of the ARGUS PRO LifeCare 2. V The transmission of ECG recordings from the ARGUS PRO LifeCare 2 is not permitted in areas in which mobile phones are not allowed.

Page 7

1 1.5

Safety Notes Safety Facilities

ARGUS PRO LifeCare 2

1.5

Safety Facilities V

Operating the device without the correctly rated fuse or with defective cables, constitutes a danger to life. Therefore: – Do not operate the unit if the earth connection is suspect or if the mains lead is damaged or suspected of being damaged. – Damaged cable connections and connectors must be replaced immediately. – The electrical safety devices, such as fuses, must not be altered. – Ruptured fuses must only be replaced with the same type and rating as the original.

1.7

Page 8

Operation with other Devices V

Accessory equipment connected to the analogue and digital interfaces must be certified according to the respective IEC standards (e.g. IEC/EN 60950 for data processing equipment and IEC/EN 60601-1 for medical equipment). Furthermore, all configurations shall comply with the valid version of the system standard IEC/EN 60601-1-1. Everybody who connects additional equipment to the signal input part or signal output part configures a medical system and is therefore responsible that the system complies with the requirements of the valid version of the system standard IEC/EN 60601-1-1. If in doubt, consult the technical service department or your local representative.

V

Any other equipment used with the patient must use the same common earth as the ARGUS PRO LifeCare 2.

V

Special care must be exercised when the unit is used with high-frequency equipment. Use the special high-frequency SCHILLER patient cable to avoid possible signal interference during ECG acquisition.

V

There is no danger when using this device simultaneously with electrical stimulation equipment. However, the stimulation units should only be used at a sufficient distance from the electrodes. If in doubt, the patient should be disconnected from the device.

V

If the device is part of a medical system, only the original SCHILLER patient cable must be used with, and connected to, the ARGUS PRO LifeCare 2.

V

If the patient cable should become defective after defibrillation, a lead-off indication is displayed on the screen and an audible alarm is issued

V

Portable communication devices, HF radios and devices labelled with the symbol (non-ionic electromagnetic radiation) can affect the operation of this device.

Networks and Internet V

When the unit is part of a network, (LAN, WLAN, HIS, etc.), transmitting over a telephone network or any other transmission/reception medium, or if exposed to the Internet or other insecure networks, appropriate security measures must be taken to protect the stored patient data.

V

Patient data security and security of the network is the sole responsibility of the user.

Art. no.: 2.540060 Rev.: b

1.6

ARGUS PRO LifeCare 2

Service Handbook

1.8

Safety Notes Maintenance

1 1.8

Maintenance V Danger of electric shock! Do not open the device. No serviceable parts inside. Refer servicing to qualified technicians authorised by SCHILLER only. V Before cleaning and to isolate the mains power supply, switch the unit off and disconnect it from the mains by removing the plug. V Do not use high-temperature sterilisation processes (such as autoclaving). Do not use E-beam or gamma radiation sterilisation. V Do not use aggressive or abrasive cleaners.

Art. no.: 2.540060 Rev.: b

V Do not, under any circumstances, immerse the device or cable assemblies in liquid.

Page 9

1 1.9

Safety Notes Safety Symbols and Pictograms

ARGUS PRO LifeCare 2

1.9

Safety Symbols and Pictograms

1.9.1

Symbols used in this document The safety level is classified according ANSI Z535.4. The following overview shows the used safety symbols and pictograms used in this manual. For a direct danger which could lead to severe personal injury or to death.

For a possibly dangerous situation, which could lead to heavy bodily injury or to death.

For a possibly dangerous situation which could lead to personal injury.

For grouped safety notes as listed in this chapter.

Used for electrical dangers, warnings and other notes in regarding operation with electricity. Note For possibly dangerous situations, which could lead to damages to property or system failure. Important or helpful user information

Reference to other guidelines

V

Observe precautions for handling electrostatic sensitive devices

Art. no.: 2.540060 Rev.: b

Used tool for the following procedure.

Page 10

ARGUS PRO LifeCare 2

Service Handbook

1.9.2

Safety Notes Safety Symbols and Pictograms

1 1.9

Symbols used on the device and on the battery The device/component can be recycled. Notified body of the CE certification(TÜV-SÜD Produkte Service GmbH)

Attention: Consult accompanying documents.

BF symbol. The signal input is BF classified.

CF symbol. The device's signal input is defibrillation protected. CF symbol. The device is classified safe for internal and external use. However, it is only defibrillation protected when used with the original SCHILLER patient cable.

Symbol for the recognition of electrical and electronic equipment. Do not dispose of the battery or the unit in household waste. Equipment/components and accessories no longer required must be disposed of in a municipally approved collection point or recycling centre. Alternatively, you can return the equipment to your supplier or SCHILLER for disposal. Improper disposal can harm the environment and human health.

Connector for the potential equalisation of the building.

IP44

The device is protected against splashing water.

Art. no.: 2.540060 Rev.: b

Follow the instructions in the documentation.

Indication of power supply. For a detailed description, see page 35.

Do not incinerate, cut or crush the battery.

Rechargable battery.

Page 11

1 1.9

Safety Notes Safety Symbols and Pictograms

ARGUS PRO LifeCare 2

Do not short-circuit the battery. Battery storage temperature: Unlimited duration: 0...+40 °C Limited to 48 hours: -20...+60 °C Expiry date of the battery. Symbol for the recognition of batteries and rechargeable batteries. Do not dispose of the battery in household waste.

1.9.3

Symbols used on the electrode package • Remove the clothes • Open the electrode package • Peel off the protective foil

Designed for single use only; do not re-use.

Do not bend packaging.

Electrode storage temperature.

Expiry date of the electrodes.

Read the user guide before use

Latex-free Use within 1 day after opening the packaging. Store in a dry location

1.9.4

Symbols used on the SpO2 sensor packaging Only to be used on patients heavier than 30 kg.

Sensor designed for children.

Page 12

Art. no.: 2.540060 Rev.: b

Protect from direct sunlight

ARGUS PRO LifeCare 2

Service Handbook

1.10

Additional Terms

1.10.1

Terms of Warranty

Safety Notes Additional Terms

1 1.10

Your SCHILLER ARGUS PRO LifeCare 2 is warranted against defects in material and manufacture for the duration of one year (as from date of purchase). Excluded from this warranty is damage caused by an accident or as a result of improper handling. The warranty entitles to free replacement of the defective part. Any liability for subsequent damage is excluded. The warranty is void if unauthorised or unqualified persons attempt to make repairs. In case of a defect, send the device to your dealer or directly to the manufacturer. The manufacturer can only be held responsible for the safety, reliability and performance of the apparatus if: • assembly operations, extensions, readjustments, modifications, or repairs are carried out by persons authorised by him, • the SCHILLER device and approved attached equipment is used in accordance with the manufacturer's instructions and • the maintenance intervals as stated in section Maintenance are observed. There are no express or implied warranties which extend beyond the warranties hereinabove set forth. SCHILLER makes no warranty of merchantability or fitness for a particular purpose with respect to the product or parts thereof.

Art. no.: 2.540060 Rev.: b

SCHILLER assumes no liability for the loss of data saved on the computer or on the device. The user is solely responsible for the data backup.

Page 13

2 2.1

Components and Operation Design

ARGUS PRO LifeCare 2

2 Components and Operation The ARGUS PRO LifeCare 2 (in this user guide referred to as APLC 2) is a patient monitoring system for vital data, featuring a defibrillator. It is designed to meet the specific needs of ground and air rescue services and in-house and inter-hospital transportation. Data is viewed on the LCD screen and optionally printed on an external thermal printer. Biocompatibility The parts of the product described in this user guide, including all accessories, that come in contact with the patient during the intended use, fulfil the biocompatibility requirements of the applicable standards. If you have questions in this matter, please contact SCHILLER.

2.1 Power supply

Design The APLC 2 is either powered by two integrated rechargeable batteries or directly by the mains (emergency power supply). The battery capacity is sufficient for: • 100 shocks with 150 joules • 4.5 hours of monitoring

Monitoring

The following parameters can be measured and displayed numerically and graphically on the 8.4” LCD display: ECG

• with 4-lead cable - leads I, II, III, aVL, aVR, aVF • with 10-lead cable - full 12-lead ECG

SpO2

SpO2 measurement and calculation of the peripheral pulse (PP); in addition, with the Masimo Rainbow“ module, SpCO, SpMet and SpHb measurement.

Invasive pressure Temperature CO2

Non invasive blood pressure - systolic, diastolic and mean pressure. Connector P1 for IBP 1 + 3, connector P2 for IBP 2 + 4 (by use of the Y cable). Two temperature inputs. Mainstream measurement: etCO2 and respiration rate (RR) calculation.

Defibrillator

The defibrillator features a biphasic pulsed defibrillation impulse – Multipulse Biowave®. The patient is defibrillated via disposable adhesive electrodes (pads) or paddles, which also acquire the ECG signal for the defibrillation analysis. The following modes of operation are available:

(Semi) Automated External Defibrillator (AED)

In AED mode, the unit monitors and analyses the ECG via the applied defibrillator electrode pads. The device identifies the connected pad type (child / adult) and analyses if defibrillation is required. The unit then selects the appropriate energy level and prompts the user with written and spoken instructions to trigger a shock, if appropriate.

Manual mode

Page 14

The user sets the energy level and decides when to release the shock.

Art. no.: 2.540060 Rev.: b

NIBP

ARGUS PRO LifeCare 2

Service Handbook

Cardioversion

Components and Operation Options

2 2.2

In the manual cardioversion mode, the device monitors and analyses the ECG directly via pads or paddles; any shocks are released via these electrodes. The user sets the energy level and sets the unit to shock. The unit monitors the ECG signal and determines the exact moment when the shock is to be delivered, synchronised with the ECG cycle. Electrical cardioversion is used to treat heart conditions such as atrial fibrillation and atrial flutter.

Transcutaneous cardiac pacemaker

The pacemaker shock is delivered using the same electrode pads (adult or child) as those used for defibrillation. The frequency and current of the pacemaker pulses are defined by the user. There are two pacemaker modes as follows:

Fix

The pacemaker pulse is delivered at a fixed frequency and energy level defined by the user.

On demand

Energy level and frequency is defined by the user. The unit monitors the ECG signal via pads and generates pacemaker pulses if the pulse rate falls below the defined value.

2.2

Options SCHILLER Charging Unit CS-1 External charging and calibrating unit for rechargeable batteries (see page 154).

Art. no.: 2.540060 Rev.: b

Resting ECG including measurement and interpretation.

Page 15

2 2.3

Components and Operation Operating Elements

ARGUS PRO LifeCare 2

2.3

Operating Elements

2.3.1

Front Battery compartment

Keys for AED mode operation 1 - 3 Keys for operation in manual defibrillation mode

Microphone Connectors left panel: • ECG • NIBP • Left paddle • Pads

Connectors right panel: • CO2 • SpO2 • Right paddle • T1 + 2 • P1 + 2

Suspend/delete alarms Event key

Rotary knob

SIM card Function keys

Menu keys

On/off key Start/stop printout

Fig. 2.1

Page 16

Operating elements APLC 2 front

Art. no.: 2.540060 Rev.: b

Paper compartment release

ARGUS PRO LifeCare 2

2.3.2 2

1

4

5

Components and Operation Operating Elements

Service Handbook

2 2.3

Connections 7

3

10

6

8

9

11

Back panel

Fig. 2.2

Connectors APLC 2 left and right panel

Left panel (1) ECG (2) Pad connector (3) Potential equalisation (4) Non-invasive blood pressure (5) Left paddle (covered if pads are connected) (6) USB connector for use with a memory stick to copy data or download software Right panel (7) CO2 capnography (8) Temperature T1 and T2 (9) Invasive blood pressure P1 and P2 (10) Pulse oximetry SpO2

Art. no.: 2.540060 Rev.: b

(11) Right paddle Back panel Emergency power supply with power supply unit connector 15 VDC, max. 6.7 A. We recommend to generally charge or operate the device via the docking station. V The plug-in connections are only designed for the connection of equipment or accessories supplied by SCHILLER. V To ensure patient's safety, neither the electrodes (including the neutral electrode) nor the patient or persons touching the patient must come into contact with conducting objects such as the USB connector, even if these are earthed.

Page 17

2 2.3

Components and Operation Operating Elements

2.3.3

ARGUS PRO LifeCare 2

Description of keys Manual printing. Printout of the vital data report including ECG curves, or the displayed data (depending on the screen), such as limit settings or trends. Settings, see page 62.

Registering events Suspension of an audible alarm or deletion of displayed messages The alarm suppression time is defined in the Settings/Alarm menu. See section 3.7 on page 43 and section 4.1.3 on page 54. Starting the automatic defibrillation mode When in the AED mode, switch to the manual mode at any time by pressing the Energy key.

Starting the analysis when in AED mode Starting the manual defibrillation mode When in the AED mode, switch to the manual mode at any time by pressing this key.

Defibrillator charging This key is only active when in the manual defibrillation mode. Shock key Triggering the shock when in the automatic or manual defibrillator mode. Rotary knob for navigation, value selection and value change. 1. 2. 3. 4.

The field or value is selected by turning the knob to the left or right. By pressing the rotary knob, the menu for the selected measurement field or value is displayed. The value is selected by turning the knob to the left or right. To apply the changed value, press the rotary knob.

Press this key to deactivate the defibrillation mode or to close any open dialogues, and to return to the monitoring display.

Starting the pacemaker mode.

Press this key to close open dialogues one by one.

Menu access Press this key to open the main menu, or, if any dialogues are displayed, return to the monitoring display.

Page 18

Art. no.: 2.540060 Rev.: b

Monitor key