Newport e360 Ventilator with Accessories Service Manual Rev B March 2019

© 2014, 2017, 2018, 2019 Covidien. All rights reserved. COVIDIEN, COVIDIEN with logo, and Covidien logo and Positive Results for Life are U.S. and internationally registered trademarks of Covidien AG. TM* brands are trademarks of their respective owners. Other brands are trademarks of a Covidien company. The ventilator should be operated and serviced only by trained professionals. Covidien’s sole responsibility with respect to the ventilator and software, and its use, is as stated in the limited warranty provided.

Table of Contents 1

Introduction

1.1 1.2 1.2.1 1.2.2 1.3 1.4 1.5 1.6 1.6.1 1.6.2 1.6.3 1.7 1.8 1.9 1.10 1.11 2

Overview... 1-1 Definitions... 1-1 Warnings, Cautions, and Notes... 1-1 Other Definitions... 1-1 General Warnings... 1-2 General Cautions... 1-3 General Note... 1-3 Service Guidelines... 1-3 Regular Service... 1-3 Complete Service Records... 1-4 Service Life... 1-4 Disclaimers... 1-4 Electromagnetic Compatibility (EMC)... 1-4 Revision History... 1-7 Warranty Information... 1-7 Contact Information... 1-8 Maintenance, Overhaul, and Software Upgrade

2.1 2.2 2.3 2.4 2.5 2.6 2.6.1 2.6.2 2.6.3 2.7 2.7.1 2.7.2 2.7.3 2.7.4 2.7.5 2.7.6 2.7.7 2.7.8 2.8 2.8.1 2.8.2 2.8.3

Overview... 2-1 Maintenance and Overhaul Intervals... 2-1 General Warnings... 2-1 General Cautions... 2-2 Tools Required... 2-2 Parts Required... 2-3 Preventive Maintenance Kit... 2-3 Overhaul Kit... 2-4 Biannual Maintenance... 2-4 Maintenance Procedures... 2-5 Inlet Water Trap Filters and O-Ring Assembly... 2-5 Exhalation Valve Adapter... 2-6 Exhalation Valve Diaphragm, Seal, and O-Ring... 2-8 Emergency Relief Diaphragm... 2-9 In-Line Disk Filters and Restrictor with Filter...2-10 Coin Battery (SBC2100P and SBC2108P)...2-11 Cooling Fan Filter and Guard...2-13 Inhalation Outlet Check Valve...2-14 Overhaul Procedures... 2-14 Inlet Water Trap Filter and O-Ring Assembly...2-14 Air and Oxygen Inlet Regulator Rebuild...2-15 Cooling Fan Filter and Guard...2-16

i

2.8.4 2.8.5 2.8.6 2.8.7 2.8.8 2.8.9 2.8.10 2.8.11 2.9 2.9.1 2.9.2 2.9.3 2.9.4 2.10 2.10.1 2.10.2 2.10.3 3

Troubleshooting

3.1 3.2 3.3

Overview... 3-1 Troubleshooting Guide... 3-1 Device Alert Messages... 3-3

4

Component Removal and Replacement

4.1 4.2 4.2.1 4.2.2 4.3 4.4 4.5 4.5.1 4.5.2 4.6 4.7 4.8 4.8.1 4.8.2 4.9 4.10 4.11 4.11.1 4.11.2

ii

Exhalation Valve Adapter...2-16 Exhalation Valve Diaphragm/Poppet Assembly...2-16 Emergency Relief Diaphragm...2-16 Emergency Intake Diaphragm...2-17 Inhalation Outlet Check Valve...2-18 In-Line Disk Filters and Restrictor with Filter...2-18 Coin Battery (SBC2100P and SBC2108P)...2-18 Coin Battery (SBC2105A)...2-18 Biannual Maintenance... 2-22 Internal Battery...2-22 Oxygen Sensor...2-22 Tubing...2-23 Upon Completion...2-23 Software Upgrade Procedure... 2-23 General Information...2-23 Upgrade Procedure...2-23 Circuit Check Test and Diagnostic...2-25

Overview... 4-1 Key Components... 4-1 Ordering... 4-1 Removing... 4-1 Preparation... 4-1 Tools Required... 4-1 Exhalation Valve and Exhalation Flow Sensor... 4-2 Valve (EXH2105A) and Flow Sensor (FLS2101P)... 4-2 Exhalation Flow Sensor Cable (Outside) (GR-CBL2123P)... 4-4 Top Cover (CVR2101M)... 4-4 Front Panel Assembly... 4-5 Main Board and Main Board Support... 4-7 Main Board (GR-PCB2100A)... 4-7 Main Board Support (CVR2103M)... 4-8 Display Board (GR-PCB2109A)... 4-9 Touch Screen Interface Board (PCB2105P) (PCB2105P-M for e360T model)... 4-11 Large LCD Cable and LCD Display... 4-11 Large LCD Cable (GR-CBL2155A)...4-11 LCD Display (10139301)...4-12

4.12 4.13 4.14 4.15 4.16 4.16.1 4.16.2 4.16.3 4.16.4 4.16.5 4.17 4.18 4.19 4.20 4.21 4.22 4.23 4.24 4.25 4.26 4.27 4.28 5

Front Panel Cover (CVR2104M)... 4-13 Optical Encoder (GR-ENC1800P)... 4-14 Alarm LEDs (GR-CBL2137A and GR-CBL2138A)... 4-14 Touch Screen (GR-PNL2105P)... 4-15 Pneumatics Panel Assembly and Components... 4-16 Panel Assembly (SVO2101A)...4-16 Air and Oxygen Inspiratory Flow Sensors (GR-FTD2100P and GR-FTD2101P)...4-19 Regulators, Inlet Blocks, and Flow Sensor Block...4-20 PSOL Valves (10113777)...4-21 Regulator and Solenoid Assembly (GR-BKT2105A)...4-23 Main Flow Outlet Block (GR-BLK2108A)... 4-24 Oxygen Sensor (SEN2103P)... 4-25 Inhalation Outlet Block and Mixing Block Assembly... 4-26 Analog Board (GR-PCB2110A)... 4-27 Heater Assembly (GR-HTR2100A)... 4-29 Exhalation Manifold... 4-30 Exhalation Flow Sensor Board (GR-PCB2103P)... 4-31 Battery (BAT2100A)... 4-32 AC/DC Power Supply (PWR2100P)... 4-33 DC to DC Power Supply (GR-PCB2101A)... 4-34 Single-Board Computer (SBC2105A)... 4-35 Power Sequence Board (GR-PCB2107A)... 4-36 Calibration Procedures

5.1 5.2 5.3 5.4 5.5 5.5.1 5.5.2 6

Overview... 5-1 Calibration Equipment... 5-1 Setup... 5-2 Diagnostic Mode... 5-3 Procedures... 5-4 Analog PCB Calibration: d5... 5-4 Pneumatics Calibration... 5-9 Operational Verification

6.1 6.2 6.3 6.4 6.4.1 6.4.2 6.5 6.5.1 6.5.2 6.5.3

Overview... 6-1 Test Equipment... 6-1 Setup... 6-2 Electrical Safety Checks... 6-3 Ground Resistance Test... 6-3 Current Leakage Test... 6-3 Operational Checks... 6-4 Front Panel LED Check... 6-5 Circuit Leak Test... 6-6 Exhalation Flow Sensor and FiO2 Sensor Calibration... 6-6

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6.5.4 6.5.5 6.5.6 6.5.7 6.5.8 6.5.9 6.5.10 6.5.11 6.5.12 6.5.13 6.5.14 6.5.15 6.5.16 6.5.17 6.5.18 A

Theory of Operations

A.1 A.2 A.2.1 A.2.2 A.2.3 A.2.4 A.3 A.3.1 A.3.2 A.4 A.4.1 A.4.2 A.4.3 A.5 A.5.1 A.5.2 A.6 A.6.1 A.6.2 A.6.3 B B.1 B.2 B.3 B.4

iv

Loss of Gas Alarm... 6-7 FiO2 Test... 6-7 Main Flow... 6-8 Bias Flow... 6-9 Inspiratory Time... 6-9 Respiratory Rate...6-10 Pressure Control...6-10 Pressure Support...6-11 Pressure Trigger Sensitivity...6-11 PEEP/CPAP...6-12 Manual Inflation...6-12 Inspiratory Tidal Volume...6-12 Expiratory Tidal Volume...6-13 Audio Paused...6-13 Loss of Power Alarm and Battery Operation...6-13

Device Description... A-1 Mandatory Breath Types... A-2 Volume Control...A-2 Pressure Control...A-3 Biphasic Pressure Release Ventilation (Open Exhalation Valve)...A-3 Volume Target (Volume Target Pressure Control-VTPC)...A-4 Spontaneous Breath Management in SIMV and SPONT Modes... A-4 Pressure Support...A-5 Volume Target Pressure Support (VTPS)...A-6 Ventilation Modes... A-7 A/CMV...A-7 SIMV...A-8 SPONT (Spontaneous)...A-9 Safety Features... A-9 Protection From Overpressurization... A-10 Protection From Rebreathing Exhaled Gases... A-10 Description of Functional Subsystems... A-10 Inhalation System... A-11 Exhalation System... A-12 Electronics... A-14 Ordering and Contact Information Ordering Parts and Kits from Customer Service... B-1 Contact Technical Support... B-4 Return Ventilator for Repair... B-4 Submit a Product Complaint... B-5

C

Diagrams

Index

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vi

List of Figures Figure 2-1. Figure 2-2. Figure 2-3. Figure 2-4. Figure 2-5. Figure 2-6. Figure 2-7. Figure 2-8. Figure 2-9. Figure 2-10. Figure 2-11. Figure 2-12. Figure 2-13. Figure 2-14. Figure 2-15. Figure 2-16. Figure 2-17. Figure 2-18. Figure 2-19. Figure 2-20. Figure 2-21. Figure 2-22. Figure 2-23. Figure 2-24. Figure 2-25. Figure 2-26. Figure 2-27. Figure 4-1. Figure 4-2. Figure 4-3. Figure 4-4. Figure 4-5. Figure 4-6. Figure 4-7. Figure 4-8. Figure 4-9. Figure 4-10. Figure 4-11. Figure 4-12. Figure 4-13. Figure 4-14. Figure 4-15. Figure 4-16.

Inlet Water Trap Filter Replacement...2-5 Exhalation Valve Adapter...2-6 Exhalation Valve Adapter Replacement...2-7 Diaphragm, Seal, and O-Ring Replacement...2-8 Inhalation Outlet Assembly...2-9 Emergency Relief Diaphragm Replacement... 2-10 JP1 at Pins 1 and 2... 2-11 J1 with CBL2132A Connected... 2-11 Verifying the Time and Date... 2-12 Filter and Guard Assembly Replacement... 2-13 Inhalation Outlet Check Valve... 2-14 Inlet Regulator Rebuild... 2-15 Emergency Intake Diaphragm and Valve Replacement... 2-17 Location of the SBC PCBA, Coin Battery, and Internal Battery... 2-19 Removing the Coin Battery... 2-20 Inserting a New Coin Battery... 2-20 Resetting the Time and Date... 2-21 Verifying the Time and Date... 2-22 Software Download / Diagnostics Mode Screen... 2-24 Event History Log Screen... 2-25 Back Panel of Ventilator... 2-26 Patient Circuit Setup... 2-27 Ventilation Standby Screen... 2-28 Circuit Check Screen... 2-28 Circuit Check Screen (Step 2)... 2-29 Technical Screen... 2-29 Diagnostic Data Screen... 2-30 Exhalation Valve and Exhalation Flow Sensor...4-3 Top Cover...4-4 Front Panel Assembly...4-5 Main Board...4-7 Main Board Support (CVR2103M)...4-8 Display Board (GR-PCB2109A)...4-9 Touch Screen Board (PCB2105P) (PCB2105P-M for e360T Model)... 4-10 Large LCD Cable (GR-CBL2155A)... 4-11 Front Panel Cover (CVR2104M)... 4-13 Touch Screen Panel (GR-PNL2105P)... 4-15 Pneumatics Cover... 4-16 Cover (CVR2115M) and Gasket (GKT2101M)... 4-17 Pneumatics Panel... 4-18 Inspiratory Flow Sensors... 4-19 Pneumatics Panel Assembly... 4-20 PSOL and Nylon String... 4-22

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Figure 4-17. Figure 4-18. Figure 4-19. Figure 4-20. Figure 4-21. Figure 4-22. Figure 4-23. Figure 4-24. Figure 4-25. Figure 4-26. Figure 4-27. Figure 4-28. Figure 4-29. Figure 4-30. Figure 5-1. Figure 5-2. Figure 5-3. Figure 5-4. Figure 6-1. Figure 6-2. Figure 6-3. Figure 6-4. Figure A-1. Figure A-2. Figure A-3. Figure A-4. Figure A-5. Figure A-6. Figure A-7. Figure C-1. Figure C-2.

viii

Regulator and Solenoid Assembly (GR-BKT2105A)... 4-23 Door (DOR2112M)... 4-24 Outlet Block (BLK2108M)... 4-25 Oxygen Sensor (SEN2103P)... 4-25 Inhalation Outlet Block and Mixing Block... 4-26 Analog Board (GR-PCB2110A)... 4-27 Heater Assembly (GR-HTR2100A)... 4-29 Location of Screws and Bumper... 4-30 Removal of Exhalation Manifold... 4-30 Exhalation Flow Sensor Board (GR-PCB2103P)... 4-31 Battery (BAT2100A)... 4-32 AC/DC Power Supply (PWR2100P)... 4-33 DC to DC Power Supply (GR-PCB2101A)... 4-34 Single-Board Computer (SBC2105A)... 4-35 Newport™ e360 Ventilator Connected to Gas Sources...5-2 Analog PCB...5-5 Air/Oxygen Pressure Regulators Adjustment... 5-11 Exhalation PSOL/Safety Regulator... 5-12 Test Setup...6-2 Front Panel Controls and Indicators...6-5 Circuit Leak Test...6-6 Pressure Control Test... 6-11 Square Waveform in VCV... A-3 Descending Ramp Flow Waveform in VCV... A-3 Pressure Overshoot... A-6 A/CMV... A-7 SIMV... A-8 Newport™ e360 Ventilator Inhalation System... A-11 Ventilator Exhalation System... A-13 Newport™ e360 Ventilator Electrical Block Diagram... C-2 Newport™ e360 Ventilator Pneumatic Diagram (SPD2100A)... C-3

List of Tables Table 1-1. Table 1-2. Table 1-3. Table 2-1. Table 2-2. Table 2-3. Table 3-1. Table 3-2. Table 5-1. Table 5-2. Table 5-3. Table 5-4. Table 5-5. Table 6-1. Table A-1. Table B-1. Table B-2.

Electromagnetic Emissions...1-5 Electromagnetic Immunity...1-5 List of Compliant Cables...1-7 Preventive Maintenance Kit Parts List...2-3 Overhaul Kit Parts List...2-4 Parts Changed During Biannual Maintenance...2-4 Troubleshooting Guide...3-1 Device Alert Messages...3-3 Diagnostic Mode...5-3 Zero Offset Calibration...5-6 Gain Calibration...5-7 Air Flow and Pressure Settings... 5-11 Oxygen Flow and Pressure Settings... 5-11 Standard Test Settings...6-4 Control Selections for Mandatory Breaths... A-2 Newport™ e360 Ventilator Spare Parts List...B-1 Newport™ e360 Ventilator Field Service Kits...B-4

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1 Introduction

1.1

Overview It is very important to read and understand all of the information in this manual before attempting to service the Newport™ e360 ventilator. Please review all warnings and cautions in this manual before attempting to service the ventilator.

1.2

Definitions

1.2.1 Warnings, Cautions, and Notes

  

WARNING: A warning describes a condition that can cause personal injury. Caution: A caution describes a condition that can cause damage to equipment. Note: A note emphasizes information that is important or convenient.

1.2.2 Other Definitions •

Inspection: Examination of actual condition.

•

Service: Measures to maintain specified condition.

•

Repair: Measures to restore to specified condition.

•

Maintenance: Inspection, service, and repair where necessary.

•

Preventive maintenance: Maintenance performed at regular intervals.

•

Operational verification: A routine verification procedure to ensure proper operation.

•

Overhaul procedure: A procedure for replacing key components at regular intervals.

1-1

Introduction

1.3

General Warnings Please review all warnings and cautions in this manual before attempting to service the ventilator. Warnings and cautions appear throughout this manual where they are relevant. The warnings and cautions listed here apply generally any time you work on the ventilator.

      

1-2

WARNING: To maintain grounding integrity, connect only to a hospital-grade receptacle. Always disconnect the power supply before servicing the ventilator. WARNING: There is a risk of explosion if used in the presence of flammable anesthetics. WARNING: Before returning to patient use, the ventilator must pass the operational verification procedure. WARNING: All ventilator service or repair must be performed by Covidien-trained service personnel. WARNING: Use extreme caution when working inside the ventilator while it is connected to a power source. WARNING: The design of the Newport™ e360 Ventilator, the operating and service manuals, and the labeling on the ventilator take into consideration that the purchase and use of the equipment is restricted to trained professionals, and that certain inherent characteristics of the ventilator are known to the operator. Instructions, warnings, and caution statements are therefore limited to the specifics of the Newport™ e360 Ventilator. WARNING: The functioning of this machine may be adversely affected by the operation of other medical equipment (such as high-frequency surgical (diathermy) equipment, defibrillators, or short-wave therapy equipment) in the vicinity.

Service Manual

General Cautions

1.4

       1.5

 1.6

General Cautions Caution: Use standard antistatic techniques when working inside the ventilator or handling any electronic parts. Caution: Clean all external parts of the ventilator prior to service. Caution: Use only dry, clean compressed air and medical-grade oxygen. Caution: Water in the air or oxygen supply can cause equipment malfunction and damage. Caution: Mains voltage must correspond to the voltage range selected on the power module of the ventilator. Always replace an open fuse with one of correct type and rating. Caution: Do not place containers of liquids near the ventilator. Liquids that get into the ventilator can cause equipment malfunction or damage. Caution: To avoid the risk of electric shock, the ventilator should not be opened by anyone other than Covidien-trained service personnel.

General Note Note: Use the tools specified in the manual to perform specific procedures.

Service Guidelines

1.6.1 Regular Service

Service must be provided at regular intervals by Covidien-trained service personnel who have received training specific to the maintenance and repair of the Newport™ e360 ventilator.

Service Manual

1-3

Introduction

1.6.2 Complete Service Records

All service performed on the ventilator must be recorded in a service log in accordance with hospital procedures and local and national regulations. 1.6.3 Service Life

The expected service life of the e360 ventilator is 10 years. The expected service life is based on the premise of normal and reasonable operation and routine maintenance of the ventilator, parts and replaceable parts. 1.7



Disclaimers WARNING: The use of accessories or cables other than those specified with the exception of parts sold by Covidien as replacements for internal components, may result in increased emissions or decreased immunity of the ventilator system.

Covidien has no responsibility for the safe operation of the Newport™ e360 ventilator if the intended use, intended user, and intended use environment requirements specified in this document are not followed. Covidien has no responsibility for the safe operation of the Newport™ e360 ventilator if operating instructions and maintenance specified in this document are not followed or if service maintenance or repairs are performed by persons who have not received the appropriate professional training. Covidien disclaims all liability for the consequences of product alterations or modifications, as well as for the consequences that might result from the combination of this ventilator with other products, whether supplied by Covidien or by other manufacturers, if such a combination is not endorsed by Covidien. 1.8

Electromagnetic Compatibility (EMC) The ventilator is suitable for prescription use only in the specified electromagnetic environments, in accordance with the IEC 60601-1-2(EN 60601-1-2) standard. The ventilator requires special precautions during installation and operation for electromagnetic compatibility. In particular, the use of nearby mobile or portable communications equipment may influence ventilator performance. The ventilator is intended for use in the electromagnetic environment specified. Users of the ventilator should ensure it is used within such an environment. Portable RF communications equipment (including peripherals such as antenna cables and external antennas) should be used no closer than 30 cm (12 inches) to any part of the e360 ventilator, including cables specified by the manufacturer, otherwise degradation of the performance of this equipment could result.

1-4

Service Manual

Electromagnetic Compatibility (EMC)



Note: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

Table 1-1. , Table 1-2. and Table 1-3. contain the manufacturer’s declarations for the ventilator system electromagnetic emissions, electromagnetic immunity, and a list of compliant cables. Table 1-1. Electromagnetic Emissions The ventilator is intended for use in the electromagnetic environment specified below. The customer or the operator of the ventilator should assure that it is used in such an environment. Phenomenon and

Compliance

Electromagnetic environment-guidance

standard Conducted and radiated RF emissions

Group 1

The ventilator uses RF energy only for its internal functions.

Class A

The ventilator is intended to be used only in a professional healthcare facility environment and not be connected to the public mains network.

CISPR 11 Harmonic distortion

Class A

IEC 61000-3-2 Voltage fluctuations and flicker

Complies

The ventilator is intended to be used only in a professional healthcare facility environment and not be connected to the public mains network.

IEC 61000-3-3

Table 1-2. Electromagnetic Immunity Phenomenon

Basic EMC standard or test method

Electrostatic discharge

IEC 61000-4-2

Electrical fast transients / bursts

IEC 61000-4-4

Immunity test levels for professional healthcare facility environment ± 8 kV contact ± 2 kV, ± 4 kV, ± 8 kV, ± 15 kV air ± 2 kV for power supply lines ± 1 kV for input/output lines 100kHz repetition frequency

Surges

IEC 61000-4-5

± 0.5 kV, ± 1 kV line-to-line ± 0.5 kV, ± 1 kV, ± 2 kV line-to-ground 0% UT1; 0.5 cycle At 0°, 45°, 90°, 135°, 180°, 225°, 270° and 315°

Voltage dips

IEC 61000-4-11

0% UT; 1 cycle and 70% UT; 25/30 cycles2 Single phase: at 0°

Voltage interruptions

Service Manual

IEC 61000-4-11

0% UT; 250/300 cycles2

1-5

Introduction

Table 1-2. Electromagnetic Immunity (Continued) Phenomenon

Rated power frequency magnetic fields

Basic EMC standard or test method IEC 61000-4-8

Immunity test levels for professional healthcare facility environment 30 A/m 50 Hz or 60 Hz 3 V rms.

Conducted disturbances induced by RF fields

IEC 61000-4-6

0.15 MHz–80 MHz 6 V rms in ISM3 bands between 0.15 MHz and 80 MHz 3 V/m

Radiated RF EM fields

IEC 61000-4-3

80 MHz–2.7 GHz 80% AM at 1 kHz

Proximity fields from RF wireless communications equipment

IEC 61000-4-3

27 V/m, 18 Hz PM4, 385 MHz 28 V/m, 18 Hz PM, 450 MHz 9 V/m, 217 Hz PM, 710 MHz 9 V/m, 217 Hz PM, 745 MHz 9 V/m, 217 Hz PM, 780 MHz 28 V/m, 18 Hz PM, 810 MHz 28 V/m, 18 Hz PM, 870 MHz 28 V/m, 18 Hz PM, 930 MHz 28 V/m, 217 Hz PM, 1720 MHz 28 V/m, 217 Hz PM, 1845 MHz 28 V/m, 217 Hz PM, 1970 MHz 28 V/m, 217 Hz PM, 2450 MHz 9 V/m, 217 Hz PM, 5240 MHz 9 V/m, 217 Hz PM, 5500 MHz 9 V/m, 217 Hz PM, 5785 MHz

1. 2. 3.

4.

1-6

UT is the AC mains voltage prior to application of the test level. 25/30 means 25 periods at 50 Hz and 30 periods at 60 Hz The ISM (industrial, scientific and medical) bands between 0,15 MHz and 80 MHz are 6,765 MHz to 6,795 MHz; 13,553 MHz to 13,567 MHz; 26,957 MHz to 27,283 MHz; and 40,66 MHz to 40,70 MHz. The amateur radio bands between 0,15 MHz and 80 MHz are 1,8 MHz to 2,0 MHz, 3,5 MHz to 4,0 MHz, 5,3 MHz to 5,4 MHz, 7 MHz to 7,3 MHz, 10,1 MHz to 10,15 MHz, 14 MHz to 14,2 MHz, 18,07 MHz to 18,17 MHz, 21,0 MHz to 21,4 MHz, 24,89 MHz to 24,99 MHz, 28,0 MHz to 29,7 MHz and 50,0 MHz to 54,0 MHz. PM is the Pulse Modulation

Service Manual

Revision History

Table 1-3. List of Compliant Cables Part number and description PWR1500P-EU, E360 power cord, European style C plug

Cable length 2.5 m (8 ft)

PWR2103P-BR, E360 power cord, Brazilian detachable cordset 250VAC, 10A

2.5 m (8 ft)

PWR1500P, E360 power cord, North American style plug

3.0 m (10 ft)

PWR290P-EU, FPD2126A power cord, European style C plug

2.5 m (8 ft)

FPD2126A-IN, 15 in. external touchscreen kit, medical grade, w/ Euro PS

4.6 m (15 ft) power cable 2.5 m (8 ft) VGA cable 2.0 m (7 ft) COM cable 4.0 m (13 ft) power cable

FPD2126A, 15 in. external touch screen kit, medical grade

2.5 m (8 ft) VGA cable 2.0 m (7 ft) COM cable

1.9

GR-CBL1829A, remote alarm cable for nurse call system

3.0 m (10 ft)

PST3600A, 110V medical-grade power strip assembly

4.6 m (15 ft)

Revision History The part number, revision level, and date on the documentation indicate its version. The revision level and date change when a new edition is printed in accordance with the revision history of the documentation. Minor corrections and updates incorporated at reprint do not cause the revision number to change. The document part number may change when extensive technical changes are incorporated into the document.

1.10

Warranty Information The information contained in this document is subject to change without notice. Covidien makes no warranty of any kind with regard to this material, including, but not limited to, the implied warranties or merchantability and fitness for a particular purpose. Covidien shall not be liable for errors contained herein or for incidental or consequential damages in connection with the furnishing, performance, or use of this material.

Service Manual

1-7

Introduction

1.11

Contact Information Technical Service Telephone: 1 800 255 6774, option #4 and option #2 Internet: www.covidien.com Email: [email protected] Manufacturer Address:15 Hampshire Street, Mansfield, MA 02048 USA EC Representative: Covidien Ireland Limited, IDA Business and Technology Park, Tullamore, Ireland.

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Service Manual