ACCLAIM encore Technical Service Manual Rev A June 2010

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Change History Part Number

Description of Change

430-96201-001 (Rev. 09/98)

Original issue

430-96201-002 (Rev. 10/98)

Second issue

430-96201-003 (Rev. 09/99)

Third issue Update Section 1.8

430-96201-004 (Rev. 08/00)

Fourth issue Update Section 4, Section 7, and Section 9

430-96201-005 (Rev. 04/05)

Fifth issue Incorporate Hospira name change

430-96201-006 (Rev. 03/10)

Sixth issue Update Electrical Safety Test Update Section 5 and Section 7

430-96201-007 (Rev. 06/10)

Seventh Issue Add Caution to Section 7

Technical Service Manual

Acclaim encore Infusion System

CHANGE HISTORY

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Acclaim encore Infusion System

Technical Service Manual

Contents Section 1 INTRODUCTION... 1.1 SCOPE... 1.2 CONVENTIONS... 1.3 ACRONYMS AND ABBREVIATIONS . . 1.4 USER QUALIFICATION... 1.5 ARTIFACTS... 1.6 ELECTROMAGNETIC COMPATIBILITY. 1.7 INFUSION SYSTEM INSTALLATION . . 1.7.1 UNPACKING... 1.7.2 INSPECTION... 1.7.3 SELF TEST... 1.8 OPTIONAL USER SETTINGS... 1.9 GENERAL SERVICE MODE...

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1-1 1-1 1-2 1-2 1-4 1-4 1-5 1-5 1-5 1-5 1-6 1-7 1-7

Section 2 WARRANTY .

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SYSTEM OPERATING MANUAL .

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3-1

THEORY OF OPERATION... 4.1 GENERAL DESCRIPTION... 4.2 ELECTRONICS OVERVIEW... 4.2.1 POWER SUPPLY PWA... 4.2.1.1 SWITCHER CIRCUITRY... 4.2.1.2 STARTUP/SHUTDOWN CIRCUITRY... 4.2.1.3 BATTERY CHARGER CIRCUITRY... 4.2.2 MCU PWA... 4.2.2.1 MICROPROCESSOR SUPERVISORY CIRCUITRY . 4.2.2.2 SERIAL COMMUNICATION CIRCUITRY... 4.2.2.3 ALARM LOGIC CIRCUITRY... 4.2.2.4 ALARM POWER BACKUP CIRCUITRY... 4.2.2.5 PROGRAMMABLE MICROCONTROLLER PERIPHERAL CIRCUITRY... 4.2.2.6 MOTOR DRIVER CIRCUITRY... 4.2.3 VOLUME CONTROL AND LOCKOUT PWA... 4.2.3.1 HIGH VOLUME AUDIBLE ALARM... 4.2.3.2 FRONT PANEL LOCKOUT SWITCH... 4.2.4 LCD PWA... 4.2.4.1 LCD DRIVER... 4.2.4.2 LED BACKLIGHT PANEL AND DRIVER... 4.2.4.3 LED INDICATOR CIRCUITRY... 4.2.4.4 KEYPAD CIRCUITRY... 4.2.5 PRESSURE SENSOR PWA... 4.2.5.1 EEPROM CIRCUITRY... 4.2.5.2 A/D CONVERTER CIRCUITRY... 4.2.5.3 BRIDGE DRIVE CIRCUITRY... 4.2.5.4 DISTAL PRESSURE AMPLIFIER CIRCUITRY . . . 4.2.5.5 PROXIMAL PRESSURE AMPLIFIER CIRCUITRY . 4.2.5.6 TEMPERATURE SENSOR CIRCUITRY...

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Section 3 Section 4

Technical Service Manual

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Acclaim encore Infusion System

CONTENTS

4.2.6 BUBBLE SENSOR PWA... 4.2.6.1 TRANSMITTER CIRCUITRY... 4.2.6.2 RECEIVER CIRCUITRY... 4.2.6.3 POSITION SENSOR CIRCUITRY... 4.3 MECHANICAL OVERVIEW... 4.3.1 MECHANISM ASSEMBLY... 4.3.1.1 MOTOR AND CRANKSHAFT/ECCENTRIC CAM ASSEMBLIES... 4.3.1.2 PUMPING HEAD... 4.3.1.3 PROXIMAL PRESSURE SENSOR... 4.3.1.4 DISTAL PRESSURE SENSOR... 4.3.1.5 ULTRASONIC AIR SENSOR... 4.3.1.6 TEMPERATURE SENSOR... 4.3.1.7 FLOOD CLAMP ACTUATOR... 4.3.1.8 ANTI FREE FLOW ACTUATOR...

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4-11 4-11 4-12 4-12 4-12 4-12

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4-13 4-13 4-13 4-13 4-14 4-14 4-14 4-14

MAINTENANCE AND SERVICE TESTS... 5.1 ROUTINE MAINTENANCE... 5.1.1 CLEANING AND SANITIZING... 5.2 PERFORMANCE VERIFICATION TEST... 5.2.1 EQUIPMENT REQUIRED... 5.2.2 INSPECTION... 5.2.3 TEST SETUP... 5.2.4 SELF TEST... 5.2.5 FREE FLOW TEST... 5.2.6 KEYPAD TEST... 5.2.7 DOOR OPEN/ALARM LOUDNESS TEST... 5.2.8 LOCKOUT SWITCH TEST... 5.2.9 PROXIMAL OCCLUSION TEST... 5.2.10 AIR-IN-LINE ALARM TEST... 5.2.11 DISTAL OCCLUSION TEST... 5.2.12 DELIVERY ACCURACY TEST... 5.2.13 BATTERY CHARGER CURRENT TEST (OPTIONAL) . 5.2.14 ELECTRICAL SAFETY TEST... 5.2.15 END OF THE PVT... 5.3 PERIODIC MAINTENANCE INSPECTION... 5.4 BATTERY OPERATION OVERVIEW...

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5-1 5-1 5-1 5-3 5-3 5-3 5-4 5-4 5-6 5-7 5-8 5-8 5-9 5-9 5-10 5-12 5-12 5-13 5-13 5-13 5-14

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6-1 6-1 6-1 6-1 6-4 6-6

Section 5

Section 6 TROUBLESHOOTING... 6.1 TECHNICAL ASSISTANCE... 6.2 ALARM MESSAGES AND ERROR CODES... 6.2.1 OPERATIONAL ALARM MESSAGES... 6.2.2 ERROR CODES REQUIRING TECHNICAL SERVICE . 6.3 TROUBLESHOOTING PROCEDURES...

Acclaim encore Infusion System

Technical Service Manual

FIGURES

Section 7 REPLACEABLE PARTS AND REPAIRS... 7.1 REPLACEABLE PARTS... 7.2 REPLACEMENT PROCEDURES... 7.2.1 SAFETY AND EQUIPMENT PRECAUTIONS... 7.2.2 REQUIRED TOOLS AND MATERIALS... 7.2.3 RUBBER FOOT PAD REPLACEMENT... 7.2.4 BATTERY, BATTERY DOOR, AND DOOR PAD REPLACEMENT . . 7.2.5 SEPARATING THE FRONT ENCLOSURE, REAR ENCLOSURE, AND MAIN CHASSIS... 7.2.6 FRONT ENCLOSURE, REAR ENCLOSURE, OR MAIN CHASSIS REPLACEMENT... 7.2.7 FRONT ENCLOSURE ASSEMBLY COMPONENT REPLACEMENT . . 7.2.7.1 LCD PWA AND RIBBON CABLE REPLACEMENT... 7.2.7.2 FRONT PANEL KEYPAD REPLACEMENT... 7.2.7.3 MECHANISM ASSEMBLY REPLACEMENT... 7.2.8 REAR ENCLOSURE ASSEMBLY COMPONENT REPLACEMENT . . 7.2.8.1 FUSE REPLACEMENT... 7.2.8.2 POWER SUPPLY PWA REPLACEMENT... 7.2.8.3 AC POWER CORD, STRAIN RELIEF BUSHING, AND VELCRO RETAINER STRAP REPLACEMENT... 7.2.8.4 VOLUME CONTROL AND LOCKOUT PWA REPLACEMENT. 7.2.8.5 POLE CLAMP EXTRUSION, BACKING PLATE, AND INSULATOR REPLACEMENT... 7.2.8.6 POLE CLAMP SHAFT/KNOB ASSEMBLY AND SHAFT TIP REPLACEMENT... 7.2.8.7 PIEZO ALARM TRANSDUCER REPLACEMENT...

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7-1 7-1 7-1 7-2 7-2 7-3 7-4

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. 7-6 . 7-7 . 7-8 . 7-9 . 7-9 . 7-10 . 7-11 . 7-12 . 7-12 . 7-13 . 7-14 . 7-16 . 7-17

Section 8 SPECIFICATIONS .

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Section 9 DRAWINGS .

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9-1

INDEX .

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Technical Service Manual

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Acclaim encore Infusion System

TABLES

Figures Figure 1-1. Figure 4-1. Figure 4-2. Figure 4-3. Figure 5-1. Figure 5-2. Figure 5-3. Figure 7-1. Figure 7-2. Figure 7-3. Figure 7-4. Figure 7-5. Figure 7-6. Figure 7-7. Figure 9-1. Figure 9-2. Figure 9-3. Figure 9-4.

Display and Keypad... H-Bridge Driver Circuit... Modulator Circuit... Chopper Motor Drive Waveforms... Display and Keypad... Free Flow Test Setup... Occlusion Test Setup... Bottom View... Front Enclosure, Main Chassis, and Rear Enclosure. Front Enclosure Assembly Components... Mechanism Assembly Replacement... Rear Enclosure Assembly Components... Volume Control and Lockout PWA Replacement . Rear Enclosure Components... Illustrated Parts Breakdown... Front Enclosure, Main Chassis, and Rear Enclosure. Front Enclosure Assembly... Rear Enclosure Assembly...

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Conventions... Optional User Settings... General Service Mode... Battery Charge Current States... Cleaning Solutions... Electrical Safety Measurements... Operational Alarm Messages and Corrective Actions . Error Codes Requiring Technical Service... Troubleshooting with the PVT... Drawings... Illustrated Parts Breakdown...

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Tables Table 1-1. Table 1-2. Table 1-3. Table 4-1. Table 5-1. Table 5-2. Table 6-1. Table 6-2. Table 6-3. Table 9-1. Table 9-2.

Acclaim encore Infusion System

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. 1-2 . 1-7 . 1-8 . 4-3 . 5-2 . 5-13 . 6-2 . 6-4 . 6-6 . 9-1 . 9-1

Technical Service Manual

Section 1

INTRODUCTION The Acclaim™ encore is an infusion system designed to meet the growing demand for hospital wide, alternate site, and home healthcare device standardization. The Acclaim encore delivers parenteral and enteral fluids and whole blood or red blood cell components using a wide variety of standard administration sets and fluid containers. These features make the Acclaim encore infusion system convenient and cost-effective.

1.1

SCOPE This manual is organized into 11 sections: ❏ Section 1 Introduction ❏ Section 2 Warranty ❏ Section 3 System Operating Manual ❏ Section 4 Theory of Operation ❏ Section 5 Maintenance and Service Tests ❏ Section 6 Troubleshooting ❏ Section 7 Replaceable Parts and Repairs ❏ Section 8 Specifications ❏ Section 9 Drawings ❏ Index ❏ Technical Service Bulletins If a problem in device operation cannot be resolved using the information in this manual, contact Hospira (see Section 6.1). Specific instructions for operating the device are contained in the Acclaim encore System Operating Manual. The terms “infusion system”, “infuser”, and “device” are used interchangeably throughout the manual. Figures are rendered as graphic representations to approximate actual product. Therefore, figures may not exactly reflect the product. Screen representations are examples only, and do not necessarily reflect the most current configuration.

Technical Service Manual

1-1

Acclaim encore Infusion System

SECTION 1 INTRODUCTION

1.2

CONVENTIONS The conventions listed in Table 1-1, are used throughout this manual. Table 1-1. Convention

Conventions

Application

Example

Blue Italic

Reference to a section, figure, or table

(see Section 6)

[ALL CAPS] in brackets

Touchswitches, keys, buttons

[START]

ALL CAPS

Screens and displayed messages

LOW BATTERY

Red Bold

Warnings and Cautions

CAUTION: Use proper ESD grounding techniques when handling components.

Throughout this manual, warnings, cautions, and notes are used to emphasize important information, as follows:

WARNING:

A WARNING CONTAINS SPECIAL SAFETY EMPHASIS AND MUST BE OBSERVED AT ALL TIMES. FAILURE TO OBSERVE A WARNING MAY RESULT IN PATIENT INJURY AND BE LIFE-THREATENING.

CAUTION: A CAUTION usually appears in front of a procedure or statement and contains information that could prevent hardware failure, irreversible damage to equipment, or loss of data.

 Note: A note highlights information that helps explain a concept or procedure. 1.3

ACRONYMS AND ABBREVIATIONS Acronyms and abbreviations used in this manual are as follows: A Ampere AC Alternating current A/D Analog-to-digital ALU Arithmetic logic unit CMOS Complementary metal oxide semiconductor COMM Communication CPU Central processing unit DC Direct current DMM Digital multimeter DPM Digital pressure meter ECG Electrocardiogram

Acclaim encore Infusion System

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Technical Service Manual

1.3

ACRONYMS AND ABBREVIATIONS

EEG Electroencephalogram EEPROM Electrically erasable/programmable read-only memory EMG Electromyogram EMI Electromagnetic interference EPROM Erasable/programmable read-only memory ESD Electrostatic discharge HKDC Housekeeping DC hr Hour IC Integrated circuit ID Identification I/O Input/output IPB Illustrated parts breakdown IV Intravenous kg Kilogram kHz Kilohertz KVO Keep vein open lbs Pounds LCD Liquid crystal display LED Light emitting diode mA Milliampere MCU Micro controller unit mg Milligram MHz Megahertz mL Milliliter mL/hr Milliliter per hour MOSFET Metal oxide semiconductor field effect transistor ms Millisecond mV Millivolt N/A Not applicable NMI Non maskable interrupt NTC Negative temperature coefficient PAL Programmable array logic PLD Programmable logic device PSI Pounds per square inch PVT Performance verification test PWA Printed wiring assembly RAM Random access memory RMS Root mean square ROM Read only memory

Technical Service Manual

1-3

Acclaim encore Infusion System

SECTION 1 INTRODUCTION

SW Switch SRAM Static random access memory V Volt VCC Collector supply voltage VCO Voltage-controlled oscillator VDC Volts DC VTBI Volume to be infused WDI Watchdog input XMIT Transmit μA Microampere μg Microgram μl Microliter μs Microseconds

1.4

USER QUALIFICATION The infusion system is intended for use at the direction or under the supervision of licensed physicians or certified healthcare professionals who are trained in the use of the infusion system and the administration of parenteral and enteral fluids and drugs, and whole blood or red blood cell components. Training should emphasize preventing related IV complications, including appropriate precautions to prevent accidental infusion of air. The epidural route can be used to provide anesthesia or analgesia.

1.5

ARTIFACTS Nonhazardous, low-level electrical potentials are commonly observed when fluids are administered using infusion devices. These potentials are well within accepted safety standards, but may create artifacts on voltage-sensing equipment such as ECG, EMG, and EEG machines. These artifacts vary at a rate that is associated with the infusion rate. If the monitoring machine is not operating correctly or has loose or defective connections to its sensing electrodes, these artifacts may be accentuated so as to simulate actual physiological signals. To determine if the abnormality in the monitoring equipment is caused by the infuser instead of some other source in the environment, set the device so that it is temporarily not delivering fluid. Disappearance of the abnormality indicates that it was probably caused by electronic noise generated by the infuser. Proper setup and maintenance of the monitoring equipment should eliminate the artifact. Refer to the appropriate monitoring system documentation for setup and maintenance instructions.

Acclaim encore Infusion System

1-4

Technical Service Manual

1.6

ELECTROMAGNETIC COMPATIBILITY

1.6

ELECTROMAGNETIC COMPATIBILITY The equipment generates, uses, and can radiate radio frequency energy and, if not installed and used in accordance with the instructions, may cause harmful interference to other devices in the vicinity. CAUTION: Portable and mobile RF communications equipment, such as cellular telephones, two-way radios, Bluetooth® devices, and microwave ovens in close proximity to the infusion system may degrade performance of the system. Operation of the infuser under such conditions should be avoided. There is a shared responsibility between manufacturers, customers, and users to assure that medical equipment and systems are designed and operated as intended. Medical electrical equipment requires special precautions regarding electromagnetic compatibility. The electromagnetic environment should be managed to permit the infusion system to perform as intended without disturbing other equipment. The infusion system should not be used adjacent to or stacked with other equipment. If the device must be used adjacent to or stacked with other equipment, monitor the equipment to assure there is no electromagnetic interference, and verify normal infuser operation.

1.7

INFUSION SYSTEM INSTALLATION CAUTION: Infusion system damage may occur unless proper care is exercised during product unpacking and installation. Accessory equipment connected to the analog and digital interfaces must be certified according to the respective IEC standards (i.e., IEC 60601-1 for medical equipment). Furthermore, all configurations shall comply with the system standard IEC 60601-1-2. Any person who connects additional equipment to the signal input or output part is configuring a medical system, and is therefore responsible for assuring that the system complies with the requirements of IEC 60601-1-2. If in doubt, contact Hospira.

1.7.1

UNPACKING Inspect the shipping container as detailed in Section 1.7.2. Use care when unpacking the infusion system. Retain the packing slip and save all packing material in the event it is necessary to return the infuser to the factory. Verify the shipping container contains a copy of the Acclaim encore System Operating Manual.

1.7.2

INSPECTION Inspect the shipping container for damage. Should any damage be found, contact the delivering carrier immediately. CAUTION: Do not use the device if it appears to be damaged. Should damage be found, contact Hospira (see Section 6.1). Inspect the infusion system periodically for signs of defects such as worn accessories, broken connections, or damaged cable assemblies. Also inspect the infuser after repair or during cleaning. Replace any damaged or defective external parts.

Technical Service Manual

1-5

Acclaim encore Infusion System

SECTION 1 INTRODUCTION

1.7.3

SELF TEST CAUTION:

Do not place the infusion system in service if the self test fails.

 Note: When plugging the device into an AC power outlet, grasp the AC power

cord plug and use a forward motion into the socket. Do not use a sideways motion. When unplugging the device, grasp the AC power cord plug and pull straight out. Do not pull out using the power cord cable and do not pull out at an angle.

To perform the self test, see Figure 1-1 and proceed as follows: 1. Connect the AC power cord to a grounded AC outlet and confirm the AC power indicator is lit. 2. Open the tubing door, insert a primed administration set into the device, and close the tubing door (see the System Operating Manual). 3. Press [ON/OFF]. The screen briefly displays all characters. Verify the screen display matches Figure 1-1. If the screen does not match Figure 1-1, contact Hospira. 4. After the infuser completes the self test, disconnect from AC power and confirm that BATTERY displays on the screen and the line power indicator turns off. 5. Reconnect the infuser to AC power and press [ON/OFF], then remove the administration set. 6. To assure the battery is fully charged, connect the AC power cord to a grounded AC outlet for a minimum of eight hours with the infuser in the charge mode (off). If an alarm condition occurs during the self test, press [ON/OFF] twice then repeat the self test. If the alarm condition recurs, note the message and take corrective action (see Section 6). Repeat the self test. If the alarm condition recurs, remove the infusion system from service and contact Hospira.

BATTERY AIR IN LINE OFF LOCKED CLEAR VTBI COMPLETE CHECK SETTINGS STOPPED KVO DOOR OCCLUSION SET PRIMARY SECONDARY DOSE UP RATE WEIGHT CONC. DILUENT TAPER DOWN

VTBI

TOTAL

TIME

TOTAL VOLUME MG/KG MG/ML/HR MCG/KG/MIN DELIVERED

SECONDARY

PRIMARY RATE

VTBI

TPN

1

DOSE CALC

ON/OFF CHARGE

RATE

VTBI

2

3

CLR VOL

4

5

6

SILENCE

7

8

9

STOP

CLR

0

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START

Figure 1-1. Acclaim encore Infusion System

Display and Keypad 1-6

Technical Service Manual

1.8

OPTIONAL USER SETTINGS

1.8

OPTIONAL USER SETTINGS There are three settings that may be changed by the user (see Table 1-2). - Distal occlusion alarm pressure level setting - Purge feature enable - Secondary piggyback alert enable

 Note: The infuser must be off to access the optional user settings. To enter optional user settings, press [ON/OFF] and, during the self test, press and hold PRIMARY [RATE] until the display blanks. To switch from occlusion level, to purge feature, to secondary piggyback alert, press PRIMARY [RATE], PRIMARY [VTBI], and SECONDARY [RATE], respectively. Cycling the power activates all setting changes. Table 1-2. Feature

Default Setting

Distal occlusion alarm pressure level setting

L2

Optional User Settings Description

Low: L1 nominal Medium: L2 nominal

Action Press PRIMARY [RATE] to toggle between L1, L2, and L3

High: L3 nominal Purge feature enable

On

The ability to purge during an air-In-line alarm

Press PRIMARY [VTBI] to toggle between On and Off

Secondary piggyback alert enable

Off

The infuser beeps five times upon completion of secondary delivery and begins primary delivery

Press SECONDARY [RATE] to toggle between On and Off

1.9

GENERAL SERVICE MODE The general service mode contains all of the features found in the optional user settings and the following features (see Table 1-3). - Software version number - Dose calculation enable (software version 2.14 or higher) - Alarm history review - Clear alarm history - Run time display - Clear battery run time - Air-in-line alarm sensitivity

 Note: The infuser must initially be off to access the general service mode. Technical Service Manual

1-7

Acclaim encore Infusion System

SECTION 1 INTRODUCTION

To access the general service mode, perform the following key sequence: 1. Press [ON/OFF] and, during the self test, press and hold [0] until the screen blanks then displays the software revision number. 2. Select the appropriate action key to review or change the desired feature. 3. To activate all setting changes, press [ON/OFF] to power off the infuser, then press [ON/OFF] again to power on the infuser. The new settings will be active.

Table 1-3.

Feature

Default Setting

General Service Mode

Description

Action

Software version number

N/A

Displays the infuser software version

Press [0]

Dose calculation (software version 2.14 or higher)

OFF

Enables/disables dose calculation feature

Press [DOSE CALC] to display the Set Dose screen Note: The Set Dose screen is only accessible from the software revision display screen Press [DOSE CALC] to toggle between on and off

Alarm history review

N/A

Displays the alarm history list

Press [STOP]

Clear alarm history

N/A

Clears the alarm history list from memory

While viewing the alarm history, press and hold [CLR] for four seconds

Run time display

N/A

Total infuser run time is displayed in the large digits and battery run time is displayed in the small digits

Press [CLEAR VOL]

Clear battery run time

N/A

Clears the battery run time to zero

While viewing the run time display, press and hold [CLR] for four seconds

Air-in-line alarm sensitivity level setting

L2

L1: Air-in-line alarms at 100 μL or greater of continuous air, or 200 μL of air in any consecutive 2 mL of fluid L2: Air-in-line alarms at 200 μL or greater of continuous air, or 500 μL of air in any consecutive 2 mL of fluid OFF: Air-in-line alarms at 1500 μL or greater of continuous air

Press SECONDARY [VTBI] Each keypress of SECONDARY [VTBI] toggles the sensitivity setting

Acclaim encore Infusion System

1-8

Technical Service Manual

Section 2

WARRANTY Subject to the terms and conditions herein, Hospira, Inc., hereinafter referred to as Hospira, warrants that (a) the product shall conform to Hospira's standard specifications and be free from defects in material and workmanship under normal use and service for a period of one year after purchase, and (b) the replaceable battery shall be free from defects in material and workmanship under normal use and service for a period of 90 days after purchase. Hospira makes no other warranties, express or implied, and specifically disclaims the implied warranties of merchantability and fitness for a particular purpose. Purchaser's exclusive remedy shall be, at Hospira's option, the repair or replacement of the product. In no event shall Hospira's liability arising out of any cause whatsoever (whether such cause be based in contract, negligence, strict liability, other tort, or otherwise) exceed the price of such product, and in no event shall Hospira be liable for incidental, consequential, or special damages or losses or for lost business, revenues, or profits. Warranty product returned to Hospira must be properly packaged and sent freight prepaid. The foregoing warranty shall be void in the event the product has been misused, damaged, altered, or used other than in accordance with product manuals so as, in Hospira's judgment, to affect its stability or reliability, or in the event the serial or lot number has been altered, effaced, or removed. The foregoing warranty shall also be void in the event any person, including the Purchaser, performs or attempts to perform any major repair or other service on the product without having been trained by an authorized representative of Hospira and using Hospira documentation and approved spare parts. For purposes of the preceding sentence, "major repair or other service" means any repair or service other than the replacement of accessory items such as batteries and detachable AC power cords. In providing any parts for repair or service of the product, Hospira shall have no responsibility or liability for the actions or inactions of the person performing such repair or service, regardless of whether such person has been trained to perform such repair or service. It is understood and acknowledged that any person other than a Hospira representative performing repair or service is not an authorized agent of Hospira.

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Acclaim encore Infusion System

SECTION 2 WARRANTY

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Section 3

SYSTEM OPERATING MANUAL A copy of the system operating manual is included with every Acclaim encore infusion system. If a copy of the system operating manual is not available, contact Hospira (see Section 6.1).

Technical Service Manual

3-1

Acclaim encore Infusion System

SECTION 3 SYSTEM OPERATING MANUAL

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Acclaim encore Infusion System

3-2

Technical Service Manual