3M Ranger Model 145 Operators Manual Rev D Sept 2016

iv

Revision History

Ranger™ Pressure Infusor Model 145

Ranger™ Pressure Infusor Model 145

1

Table of Contents

Revision History Revision Reason for Change

Table of Contents

Pages Affected

Date

A

New Revision - First Release

All

May 2013

B

Translations Added

All

Jul 2013

C

Added UL 3rd edition requirements

All

Feb 2014

D

Updated to circular font and updated illustrations.

All

Sept 2016

Section 1: Technical Service and Order Placement... 2 Technical service and order placement... 2 USA... 2 Proper use and maintenance... 2 When you call for technical support... 2 Servicing... 2 Section 2: Introduction... 3 Indications for use... 3 Explanation of symbols... 3 Explanation of signal word consequences... 4 WARNING:... 4 CAUTION:... 5 NOTICE:... 5 Product description... 6 Pressure infusor panel... 7 Section 3: Instructions for Use... 9 Attaching the pressure infusor to the I.V. pole... 9 Load and pressurize the infusors... 10 Changing a fluid bag... 10 Section 4: Troubleshooting... 11 Standby/ON mode... 11 Pressure infusor... 12 Section 5: Maintenance and Storage... 13 Cleaning the Ranger pressure infusor... 13 Cleaning the pressure infusor and cord... 13 Storage... 13 Section 6: Specifications... 14 Physical characteristics... 16 Electrical characteristics... 17 Storage and transport conditions... 17 Performance characteristics... 17

English

34-8719-2475-8

4430011 Description: 3M TM Ranger™ Pressure Infusor Model 145 Operator’s Manual

Supersedes#:XX-XXXX-XXXX-X

Base File Name: PA: 34871924758.indd GA: Software: InDesign CC 2014 SGS Contact: Email: Printer: Printer Location: Supplier:

PROCESS BLACK

PROCESS CYAN

PROCESS MAGENTA

Structure#:SS-65119 Cat/Product#:145 Reference: #### Requester: Debra Staack Die # / Doc. Size: 8.5" x 11"

PROCESS YELLOW

3

Item Spec#: 34-8719-2475-8

PANTONE 5265

SILVER

PDF Scaled at 65%

3M RED

09.07.16 PU 34871533872 (3963313) make changes per annotated PDF.

TN

09.12.16 Convert all languages to 3M Circular font. 09.21.16 Add charts from referenced files 09.28.16 Final release.

TN kmh DJ

2

Technical Service and Order Placement

Ranger™ Pressure Infusor Model 145

Section 1: Technical Service and Order Placement

Technical service and order placement

Introduction

3

Section 2: Introduction

Indications for use The 3M™ Ranger™ pressure infusor is intended to provide pressure to I.V. solution bags when rapid infusion of liquids is required.

USA TEL:

Ranger™ Pressure Infusor Model 145

1-800-228-3957

Proper use and maintenance

Explanation of symbols The following symbols may appear on the product’s labeling or exterior packaging.

3M assumes no responsibility for the reliability, performance, or safety of the Ranger pressure infusor system if any of the following events occur:

Power ON

• Modifications or repairs are performed by unqualified personnel. • The unit is used in a manner other than that described in the operator’s manual or maintenance guide.

Power OFF

• The unit is installed in an environment that does not meet the appropriate electrical and grounding requirements. Standby

When you call for technical support We will need to know the serial number of your unit when you call us. The serial number label is located on the back of the pressure infusor system.

Date of manufacture

Servicing

Manufacturer

All service must be performed by 3M Health Care or an authorized service technician. Call 3M Health Care technical service at 800-228-3957 for service information. Outside of the U.S. contact your local 3M Health Care representative.

Protective earth (Ground)

CAUTION

This system is subject to the European WEEE Directive 2002/96/EC. This product contains electrical and electronic components and must not be disposed of using standard refuse collection. Please consult local directives for disposal of electrical and electronic equipment.

Defibrillation-proof type BF applied part

Voltage, alternating current (AC)

Drip proof protection of fluids

An equipotentiality plug (grounded) conductor other than a protective earth conductor or a neutral conductor, providing a direct connection between electrical equipment and the potential equalization busbar of the electrical installation. Please consult IEC 60601-1; 2005 for requirements.

CAUTION: Recycle to avoid environmental contamination This product contains recyclable parts. For information on recycling - please contact your nearest 3M Service Center for advice.

Technical Service and Order Placement 34-8719-2475-8

English

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2

Technical Service and Order Placement

Ranger™ Pressure Infusor Model 145

Section 1: Technical Service and Order Placement

Technical service and order placement

Introduction

3

Section 2: Introduction

Indications for use The 3M™ Ranger™ pressure infusor is intended to provide pressure to I.V. solution bags when rapid infusion of liquids is required.

USA TEL:

Ranger™ Pressure Infusor Model 145

1-800-228-3957

Proper use and maintenance

Explanation of symbols The following symbols may appear on the product’s labeling or exterior packaging.

3M assumes no responsibility for the reliability, performance, or safety of the Ranger pressure infusor system if any of the following events occur:

Power ON

• Modifications or repairs are performed by unqualified personnel. • The unit is used in a manner other than that described in the operator’s manual or maintenance guide.

Power OFF

• The unit is installed in an environment that does not meet the appropriate electrical and grounding requirements. Standby

When you call for technical support We will need to know the serial number of your unit when you call us. The serial number label is located on the back of the pressure infusor system.

Date of manufacture

Servicing

Manufacturer

All service must be performed by 3M Health Care or an authorized service technician. Call 3M Health Care technical service at 800-228-3957 for service information. Outside of the U.S. contact your local 3M Health Care representative.

Protective earth (Ground)

CAUTION

This system is subject to the European WEEE Directive 2002/96/EC. This product contains electrical and electronic components and must not be disposed of using standard refuse collection. Please consult local directives for disposal of electrical and electronic equipment.

Defibrillation-proof type BF applied part

Voltage, alternating current (AC)

Drip proof protection of fluids

An equipotentiality plug (grounded) conductor other than a protective earth conductor or a neutral conductor, providing a direct connection between electrical equipment and the potential equalization busbar of the electrical installation. Please consult IEC 60601-1; 2005 for requirements.

CAUTION: Recycle to avoid environmental contamination This product contains recyclable parts. For information on recycling - please contact your nearest 3M Service Center for advice.

Technical Service and Order Placement 34-8719-2475-8

English

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4

Introduction

Ranger™ Pressure Infusor Model 145

Fuse

Follow instructions for use

Ranger™ Pressure Infusor Model 145

Introduction

5

CAUTION: 1. To reduce the risks associated with instability, impact and facility medical device damage: • Mount the Ranger pressure infusor Model 145 on only a 3M model 90068/90124 pressure infusor I.V. pole/ base. • Do not mount this unit more than 56” (142 cm) from the floor to the base of the pressure infusor unit. • Do not use the power cord to transport or move the device.

Consult instructions for use

• Ensure the power cord is free from the castors during transport of the device. • Do not push on surfaces identified with the pushing prohibited symbol. Keep dry

Temperature limits

• Do not pull the I.V. pole using the pressure infusor power cord. 2. To reduce the risks associated with environmental contamination: • Follow applicable regulations when disposing of this device or any of its electronic components. 3. This product is designed for pressure infusion only.

Pushing prohibited

NOTICE: 1.

Explanation of signal word consequences

To avoid device damage: • Do not immerse the Ranger pressure infusor, pressure infusor parts, or accessories in any liquid or cleaning or disinfecting solutions. The unit is not liquid proof. • Do not spray cleaning solutions onto the pressure infusor.

WARNING: Indicates a hazardous situation which, if not avoided, could result in death or serious injury.

CAUTION: Indicates a hazardous situation which, if not avoided, could result in minor or moderate injury.

NOTICE: Indicates a situation which, if not avoided, could result in property damage only.

• Do not clean the pressure infusor with abrasive cleaners or solvents such as acetone or thinner. Damage to the case, label, and internal components may result. • Do not sterilize the pressure infusor. 2. Federal law (USA) restricts this device to sale by or on the order of a licensed healthcare professional. 3. The Ranger pressure infusor meets medical electronic interference requirements. If radio frequency interference with other equipment should occur, connect the pressure infusor to a different power source. 4. Device operating should include sufficient light so all labels, buttons, LEDs and interfaces can be read and/or interpreted clearly. The operator may need to position themselves so that light shadows do not compromise the legibility of the label on the back of the device.

WARNING: 1. To reduce the risks associated with hazardous voltage and fire: • Connect power cord to receptacles marked “Hospital Only,” “Hospital Grade,” or a reliably grounded outlet. Do not use extension cords or multiple portable power socket outlets. • Do not position the equipment where unplugging is difficult. The plug serves as the disconnect device. • Use only the power cord specified for this product and certified for the country of use. • Examine the pressure infusor for physical damage before each use. Never operate the equipment if the pressure infusor housing, power cord, or plug is visibly damaged. Contact 3M technical support at 1-800-228-3957. • Do not allow the power cord to get wet. • Do not attempt to open the equipment or service the unit yourself. Contact 3M technical support at 1-800-228-3957. • Do not modify any part of the pressure infusor. • Do not pinch the power cord of the pressure infusor when attaching other devices to the I.V. pole. 2. To reduce the risks associated with exposure to biohazards: • Always perform the decontamination procedure prior to returning the pressure infusor for service and prior to disposal. 3. To reduce the risks associated with air embolism and incorrect routing of fluids: • Never infuse fluids if air bubbles are present in the fluid line. • Ensure all luer connections are tightened.

English

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4

Introduction

Ranger™ Pressure Infusor Model 145

Fuse

Follow instructions for use

Ranger™ Pressure Infusor Model 145

Introduction

5

CAUTION: 1. To reduce the risks associated with instability, impact and facility medical device damage: • Mount the Ranger pressure infusor Model 145 on only a 3M model 90068/90124 pressure infusor I.V. pole/ base. • Do not mount this unit more than 56” (142 cm) from the floor to the base of the pressure infusor unit. • Do not use the power cord to transport or move the device.

Consult instructions for use

• Ensure the power cord is free from the castors during transport of the device. • Do not push on surfaces identified with the pushing prohibited symbol. Keep dry

Temperature limits

• Do not pull the I.V. pole using the pressure infusor power cord. 2. To reduce the risks associated with environmental contamination: • Follow applicable regulations when disposing of this device or any of its electronic components. 3. This product is designed for pressure infusion only.

Pushing prohibited

NOTICE: 1.

Explanation of signal word consequences

To avoid device damage: • Do not immerse the Ranger pressure infusor, pressure infusor parts, or accessories in any liquid or cleaning or disinfecting solutions. The unit is not liquid proof. • Do not spray cleaning solutions onto the pressure infusor.

WARNING: Indicates a hazardous situation which, if not avoided, could result in death or serious injury.

CAUTION: Indicates a hazardous situation which, if not avoided, could result in minor or moderate injury.

NOTICE: Indicates a situation which, if not avoided, could result in property damage only.

• Do not clean the pressure infusor with abrasive cleaners or solvents such as acetone or thinner. Damage to the case, label, and internal components may result. • Do not sterilize the pressure infusor. 2. Federal law (USA) restricts this device to sale by or on the order of a licensed healthcare professional. 3. The Ranger pressure infusor meets medical electronic interference requirements. If radio frequency interference with other equipment should occur, connect the pressure infusor to a different power source. 4. Device operating should include sufficient light so all labels, buttons, LEDs and interfaces can be read and/or interpreted clearly. The operator may need to position themselves so that light shadows do not compromise the legibility of the label on the back of the device.

WARNING: 1. To reduce the risks associated with hazardous voltage and fire: • Connect power cord to receptacles marked “Hospital Only,” “Hospital Grade,” or a reliably grounded outlet. Do not use extension cords or multiple portable power socket outlets. • Do not position the equipment where unplugging is difficult. The plug serves as the disconnect device. • Use only the power cord specified for this product and certified for the country of use. • Examine the pressure infusor for physical damage before each use. Never operate the equipment if the pressure infusor housing, power cord, or plug is visibly damaged. Contact 3M technical support at 1-800-228-3957. • Do not allow the power cord to get wet. • Do not attempt to open the equipment or service the unit yourself. Contact 3M technical support at 1-800-228-3957. • Do not modify any part of the pressure infusor. • Do not pinch the power cord of the pressure infusor when attaching other devices to the I.V. pole. 2. To reduce the risks associated with exposure to biohazards: • Always perform the decontamination procedure prior to returning the pressure infusor for service and prior to disposal. 3. To reduce the risks associated with air embolism and incorrect routing of fluids: • Never infuse fluids if air bubbles are present in the fluid line. • Ensure all luer connections are tightened.

English

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6

Introduction

Ranger™ Pressure Infusor Model 145

Ranger™ Pressure Infusor Model 145

Introduction

7

Pressure infusor panel

Product description The Ranger pressure infusor consists of the pressure infusor device, which is combined with user supplied intravenous (IV) fluid bags which are pressurized in the infusor’s chambers. The Ranger pressure infusor also requires user supplied disposable, sterile patient administration sets that can deliver the bag fluid to the patient under pressures up to 300 mmHg. The pressure infusor accepts solution bags ranging from 250 mL to 1000 mL. Fluids for use with the pressure infusor include, but are not limited to blood, saline, sterile water, and irrigation solution. The pressure infusor is intended to be used only with fluid bags that meet the standards of the American Association of Blood Banks. The pressure infusor is not intended for use with fluid bags and administration sets that do not meet the above specifications.

The pressure infusor panel displays the status of the pressure infusors. When the pressure infusor is initially turned ON, the indicators will illuminate to show operation. The pressure infusor power indicator illuminates yellow (standby) when the main power switch is turned ON and the pressure infusors are able to be turned ON. A green LED indicates that the infusor is ON. To pressurize/depressurize the pressure infusor, verify the pressure infusor door is closed and latched, then press the pressure infusor start/stop button. Each pressure infusor is controlled independently.

3M™ Ranger™

The Ranger pressure infusor is intended for pediatric to adult patients undergoing a medical procedure. Patients may be awake or fully anesthetized but are typically immobile on a gurney or surgical table. The fluids infused may interact with any part of the body as determined by the medical professional. The pressure infusor system is attached to a custom I.V. pole and the power cord is secured allowing the system to be moved around the hospital/healthcare facility to various locations where needed. The system is designed for frequent use whenever pressure infusion is necessary.

Pressure Infuser High

High

For operation, the Ranger pressure infusor is mounted on the I.V. pole and base that is included with the pressure infusor. A fluid bag is placed in one of the pressure infusor chambers, the infusor’s main power switch is turned ON, and the infusor chambers are activated using the user interface at the front of the device. Upon activation, the air is routed to the pressure infusor bladder, the bladder begins to inflate and pressurize the fluid bag. The user interface indicates when the fluid bag pressure is In Range and ready for use.

In Range

300 mm Hg

In Range

Note: The solution pressure of the Ranger pressure infusor is dependent on surface area and volume of the solution bag. To verify the pressure, refer to the Maintenance Guide. The Ranger pressure infusor has no user-adjustable controls. The user slides an I.V. solution bag behind the metal fingers and against the inflation bladder located inside the pressure infusor. The Ranger pressure infusor should only be used in healthcare facilities by trained medical professionals and can be used within the patient environment.

3M™ Ranger™ Pressure Infusor High

In Range

When the infusor is attached to an external power source and the main power switch is turned ON, pushing the pressure infusor start/stop button ON inflates the inflation bladder and maintains pressure on blood and solution bags. Turning the pressure infusor start/stop button OFF deflates the bladder. Turn the main power switch OFF when the pressure infusor is not in use.

Low

Low

Low

High

300 mmHg

In Range

Low

3M™ Ranger™

Pressure Infusor Power Main power switch

Power entry module

no power to unit

standby

ON

The indicator on the start/stop button notifies the user of the status of each pressure infusor. No light indicates that the unit is either not plugged in, the main power switch is not turned ON, or there is a system fault. See “Section 4: Troubleshooting” on 11 for more information.

A yellow indicator notifies the user that the pressure infusor is in standby mode and is ready to be turned ON.

A green indicator notifies the user that the infusor is pressurized.

English

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6

Introduction

Ranger™ Pressure Infusor Model 145

Ranger™ Pressure Infusor Model 145

Introduction

7

Pressure infusor panel

Product description The Ranger pressure infusor consists of the pressure infusor device, which is combined with user supplied intravenous (IV) fluid bags which are pressurized in the infusor’s chambers. The Ranger pressure infusor also requires user supplied disposable, sterile patient administration sets that can deliver the bag fluid to the patient under pressures up to 300 mmHg. The pressure infusor accepts solution bags ranging from 250 mL to 1000 mL. Fluids for use with the pressure infusor include, but are not limited to blood, saline, sterile water, and irrigation solution. The pressure infusor is intended to be used only with fluid bags that meet the standards of the American Association of Blood Banks. The pressure infusor is not intended for use with fluid bags and administration sets that do not meet the above specifications.

The pressure infusor panel displays the status of the pressure infusors. When the pressure infusor is initially turned ON, the indicators will illuminate to show operation. The pressure infusor power indicator illuminates yellow (standby) when the main power switch is turned ON and the pressure infusors are able to be turned ON. A green LED indicates that the infusor is ON. To pressurize/depressurize the pressure infusor, verify the pressure infusor door is closed and latched, then press the pressure infusor start/stop button. Each pressure infusor is controlled independently.

3M™ Ranger™

The Ranger pressure infusor is intended for pediatric to adult patients undergoing a medical procedure. Patients may be awake or fully anesthetized but are typically immobile on a gurney or surgical table. The fluids infused may interact with any part of the body as determined by the medical professional. The pressure infusor system is attached to a custom I.V. pole and the power cord is secured allowing the system to be moved around the hospital/healthcare facility to various locations where needed. The system is designed for frequent use whenever pressure infusion is necessary.

Pressure Infuser High

High

For operation, the Ranger pressure infusor is mounted on the I.V. pole and base that is included with the pressure infusor. A fluid bag is placed in one of the pressure infusor chambers, the infusor’s main power switch is turned ON, and the infusor chambers are activated using the user interface at the front of the device. Upon activation, the air is routed to the pressure infusor bladder, the bladder begins to inflate and pressurize the fluid bag. The user interface indicates when the fluid bag pressure is In Range and ready for use.

In Range

300 mm Hg

In Range

Note: The solution pressure of the Ranger pressure infusor is dependent on surface area and volume of the solution bag. To verify the pressure, refer to the Maintenance Guide. The Ranger pressure infusor has no user-adjustable controls. The user slides an I.V. solution bag behind the metal fingers and against the inflation bladder located inside the pressure infusor. The Ranger pressure infusor should only be used in healthcare facilities by trained medical professionals and can be used within the patient environment.

3M™ Ranger™ Pressure Infusor High

In Range

When the infusor is attached to an external power source and the main power switch is turned ON, pushing the pressure infusor start/stop button ON inflates the inflation bladder and maintains pressure on blood and solution bags. Turning the pressure infusor start/stop button OFF deflates the bladder. Turn the main power switch OFF when the pressure infusor is not in use.

Low

Low

Low

High

300 mmHg

In Range

Low

3M™ Ranger™

Pressure Infusor Power Main power switch

Power entry module

no power to unit

standby

ON

The indicator on the start/stop button notifies the user of the status of each pressure infusor. No light indicates that the unit is either not plugged in, the main power switch is not turned ON, or there is a system fault. See “Section 4: Troubleshooting” on 11 for more information.

A yellow indicator notifies the user that the pressure infusor is in standby mode and is ready to be turned ON.

A green indicator notifies the user that the infusor is pressurized.

English

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8

Introduction

Ranger™ Pressure Infusor Model 145

3M™ Ranger™ Pressure Infuser

Ranger™ Pressure Infusor Model 145

Instructions for Use

9

Section 3: Instructions for Use NOTE: Assemble the model 90068/90124 pressure infusor I.V. pole/base according to the instructions for use that accompanies the I.V. pole base. NOTE: Assembly of the I.V. pole/base and attachment of the pressure infusor to the I.V. pole should only be performed by a qualified, medical equipment service technician.

High

High

Attaching the pressure infusor to the I.V. pole 1.

In Range

300 mm Hg

In Range

Mount the Model 145 pressure infusor onto a Model 90068/90124 pressure infusor I.V. pole/base with locking casters as shown below.

CAUTION: To reduce the risks associated with instability and facility medical device damage:

Low

• Do not mount this unit more than 56” (142 cm) from the floor to the base of the pressure infusor.

Low 2.

Securely fasten the clamps at the back of the infusor and tighten the knob screws until the infusor is stable.

3.

Using the provided hook-and-loop strap, secure the power cord to the lower portion of the I.V. pole.

High Visual and audible indicator: The High yellow indicator illuminates and an audible indicator notifies the user when the pressure infusor bladder is above 330 mmHg. The visual and audible indicator will continue as long as the pressure remains above 330 mmHg. If the High condition is observed, the infusor chamber should be turned OFF by using the pressure infusor start/stop button. Use of the infusor chamber should be discontinued immediately, and 3M Patient Warming technical support contacted for repair and servicing.

In Range Visual only: The In Range green indicator flashes as the pressure is increasing in the pressure infusor. Once the pressure is within the target range of 230-330 mmHg, the indicator will be at a consistent green.

Low: Visual and audible indicator: The Low yellow indicator illuminates and an audible indicator notifies the user when the pressure infusor bladder has not reached 230 mmHg within approximately 30 seconds or when the pressure drops below 230 mmHg during use.

English

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8

Introduction

Ranger™ Pressure Infusor Model 145

3M™ Ranger™ Pressure Infuser

Ranger™ Pressure Infusor Model 145

Instructions for Use

9

Section 3: Instructions for Use NOTE: Assemble the model 90068/90124 pressure infusor I.V. pole/base according to the instructions for use that accompanies the I.V. pole base. NOTE: Assembly of the I.V. pole/base and attachment of the pressure infusor to the I.V. pole should only be performed by a qualified, medical equipment service technician.

High

High

Attaching the pressure infusor to the I.V. pole 1.

In Range

300 mm Hg

In Range

Mount the Model 145 pressure infusor onto a Model 90068/90124 pressure infusor I.V. pole/base with locking casters as shown below.

CAUTION: To reduce the risks associated with instability and facility medical device damage:

Low

• Do not mount this unit more than 56” (142 cm) from the floor to the base of the pressure infusor.

Low 2.

Securely fasten the clamps at the back of the infusor and tighten the knob screws until the infusor is stable.

3.

Using the provided hook-and-loop strap, secure the power cord to the lower portion of the I.V. pole.

High Visual and audible indicator: The High yellow indicator illuminates and an audible indicator notifies the user when the pressure infusor bladder is above 330 mmHg. The visual and audible indicator will continue as long as the pressure remains above 330 mmHg. If the High condition is observed, the infusor chamber should be turned OFF by using the pressure infusor start/stop button. Use of the infusor chamber should be discontinued immediately, and 3M Patient Warming technical support contacted for repair and servicing.

In Range Visual only: The In Range green indicator flashes as the pressure is increasing in the pressure infusor. Once the pressure is within the target range of 230-330 mmHg, the indicator will be at a consistent green.

Low: Visual and audible indicator: The Low yellow indicator illuminates and an audible indicator notifies the user when the pressure infusor bladder has not reached 230 mmHg within approximately 30 seconds or when the pressure drops below 230 mmHg during use.

English

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10

Instructions for Use

Ranger™ Pressure Infusor Model 145

Load and pressurize the infusors 1. Plug the power cord into an appropriately grounded outlet. 2. Using the main power switch located under the pressure infusor, turn the unit ON. 3. Remove excess air from I.V. fluid bags and prime. 4. Open pressure infusor door. 5. Slide fluid bag to the bottom of the pressure infusor ensuring bag is completely inside the metal fingers. Note: Ensure solution bag port and spike hang below the pressure infusor fingers. 6. 7.

Securely close and latch the pressure infusor door. Prime the warming set. For more information about priming the set, refer to instructions provided with the warming sets. 8. Press the pressure infusor start/stop button on the pressure infusor control panel to turn the corresponding pressure chamber ON. Note: A pressure infusor can only be turned ON when the start/stop button display status indicator is yellow. A green display status indicator notifies the infusor chamber is ON. After pressing the start/stop button, the infusor indicator LED should be flashing green in the In Range status. When the indicator LED is solid green, open clamps to begin flow. 10. To depressurize, press the pressure infusor power button on the pressure infusor control panel to turn the corresponding pressure chamber off.

Ranger™ Pressure Infusor Model 145 Operator’s Manual

Section 4: Troubleshooting

Standby/ON mode Condition

Cause

Solution

Nothing illuminates on the pressure infusor control panel when the main power switch is turned ON.

Power cord is not plugged into the power entry module, or power cord is not plugged into an appropriately grounded outlet.

Make sure the power cord is plugged into the power entry module of the pressure infusor. Make sure the pressure infusor is plugged into a properly grounded outlet.

Power LED status lights do not illuminate.

1.

Press the pressure infusor button on the pressure infusor control panel to turn the corresponding pressure chamber OFF. 2. Close pinch clamps on tubing. 3. Open pressure infusor door and remove fluid bag. 4. Remove the spike from the used fluid bag. 5. Remove air from the new fluid bag. 6. Insert spike into the new I.V. bag port. 7. Push the pressure infusor’s bladder to expel the remaining air and slide solution bag to the bottom of the pressure infusor, ensuring bag is completely inside the metal fingers. Note: Ensure fluid bag port and spike hang below the pressure infusor fingers. 8. 9.

Securely close and latch the pressure infusor door. Prime the warming set. For more information about priming the set, refer to instructions provided with the warming sets. 10. Press the pressure infusor start/stop button on the pressure infusor control panel to turn the corresponding pressure chamber ON. Note: A pressure infusor can only be turned on when the start/stop button display status indicator is yellow. A green display status indicator notifies the infusor chamber is ON. 11. 12.

11

All repair, calibration, and servicing of the Ranger pressure infusor requires the skill of a qualified, medical equipment service technician who is familiar with good practice for medical unit repair. All repairs and maintenance should be in accordance with manufacturer’s instructions. Service the Ranger pressure infusor every six months or whenever service is needed. For replacement of the Ranger pressure infusor door latch, door, bladder, fingers, or power cord, contact a biomedical technician. For additional technical support contact 3M patient warming.

9.

Changing a fluid bag

Troubleshooting

The status indicators (Low, In Range, and/or High) do not illuminate when the pressure infusor start/stop button is pushed.

Once the pressure infusor is In Range, open clamps to resume flow from the new bag of fluid. Discard fluid bags and warming sets according to institutional protocol.

Troubleshooting

34-8719-2475-8

Burned out LED light(s).

Contact a biomedical technician.

Unit failure.

Contact a biomedical technician.

Blown fuse.

Contact a biomedical technician.

Power cord is not plugged into the power entry module, or power cord is not plugged into an appropriately grounded outlet.

Make sure the power cord is plugged into the power entry module of the pressure infusor. Make sure the pressure infusor is plugged into a properly grounded outlet.

Unit is not turned ON.

Using the main power switch located under the pressure infusor turn the unit ON.

Burned out LED light.

Push the pressure infusor start/stop button, if unit functions properly, continue use. Contact a biomedical technician after use to replace LED.

Unit failure.

Contact a biomedical technician.

Blown fuse.

Contact a biomedical technician.

Power cord is not plugged into the power entry module, or power cord is not plugged into an appropriately grounded outlet.

Make sure the power cord is plugged into the power entry module of the pressure infusor. Make sure the pressure infusor is plugged into a properly grounded outlet.

Unit is not turned ON.

Using the main power switch located under the pressure infusor turn the unit ON.

Burned out LED light(s).

Contact a biomedical technician.

Unit failure.

Contact a biomedical technician.

Blown fuse.

Contact a biomedical technician.

10

Instructions for Use

Ranger™ Pressure Infusor Model 145

Load and pressurize the infusors 1. Plug the power cord into an appropriately grounded outlet. 2. Using the main power switch located under the pressure infusor, turn the unit ON. 3. Remove excess air from I.V. fluid bags and prime. 4. Open pressure infusor door. 5. Slide fluid bag to the bottom of the pressure infusor ensuring bag is completely inside the metal fingers. Note: Ensure solution bag port and spike hang below the pressure infusor fingers. 6. 7.

Securely close and latch the pressure infusor door. Prime the warming set. For more information about priming the set, refer to instructions provided with the warming sets. 8. Press the pressure infusor start/stop button on the pressure infusor control panel to turn the corresponding pressure chamber ON. Note: A pressure infusor can only be turned ON when the start/stop button display status indicator is yellow. A green display status indicator notifies the infusor chamber is ON. After pressing the start/stop button, the infusor indicator LED should be flashing green in the In Range status. When the indicator LED is solid green, open clamps to begin flow. 10. To depressurize, press the pressure infusor power button on the pressure infusor control panel to turn the corresponding pressure chamber off.

Ranger™ Pressure Infusor Model 145 Operator’s Manual

Section 4: Troubleshooting

Standby/ON mode Condition

Cause

Solution

Nothing illuminates on the pressure infusor control panel when the main power switch is turned ON.

Power cord is not plugged into the power entry module, or power cord is not plugged into an appropriately grounded outlet.

Make sure the power cord is plugged into the power entry module of the pressure infusor. Make sure the pressure infusor is plugged into a properly grounded outlet.

Power LED status lights do not illuminate.

1.

Press the pressure infusor button on the pressure infusor control panel to turn the corresponding pressure chamber OFF. 2. Close pinch clamps on tubing. 3. Open pressure infusor door and remove fluid bag. 4. Remove the spike from the used fluid bag. 5. Remove air from the new fluid bag. 6. Insert spike into the new I.V. bag port. 7. Push the pressure infusor’s bladder to expel the remaining air and slide solution bag to the bottom of the pressure infusor, ensuring bag is completely inside the metal fingers. Note: Ensure fluid bag port and spike hang below the pressure infusor fingers. 8. 9.

Securely close and latch the pressure infusor door. Prime the warming set. For more information about priming the set, refer to instructions provided with the warming sets. 10. Press the pressure infusor start/stop button on the pressure infusor control panel to turn the corresponding pressure chamber ON. Note: A pressure infusor can only be turned on when the start/stop button display status indicator is yellow. A green display status indicator notifies the infusor chamber is ON. 11. 12.

11

All repair, calibration, and servicing of the Ranger pressure infusor requires the skill of a qualified, medical equipment service technician who is familiar with good practice for medical unit repair. All repairs and maintenance should be in accordance with manufacturer’s instructions. Service the Ranger pressure infusor every six months or whenever service is needed. For replacement of the Ranger pressure infusor door latch, door, bladder, fingers, or power cord, contact a biomedical technician. For additional technical support contact 3M patient warming.

9.

Changing a fluid bag

Troubleshooting

The status indicators (Low, In Range, and/or High) do not illuminate when the pressure infusor start/stop button is pushed.

Once the pressure infusor is In Range, open clamps to resume flow from the new bag of fluid. Discard fluid bags and warming sets according to institutional protocol.

Troubleshooting

34-8719-2475-8

Burned out LED light(s).

Contact a biomedical technician.

Unit failure.

Contact a biomedical technician.

Blown fuse.

Contact a biomedical technician.

Power cord is not plugged into the power entry module, or power cord is not plugged into an appropriately grounded outlet.

Make sure the power cord is plugged into the power entry module of the pressure infusor. Make sure the pressure infusor is plugged into a properly grounded outlet.

Unit is not turned ON.

Using the main power switch located under the pressure infusor turn the unit ON.

Burned out LED light.

Push the pressure infusor start/stop button, if unit functions properly, continue use. Contact a biomedical technician after use to replace LED.

Unit failure.

Contact a biomedical technician.

Blown fuse.

Contact a biomedical technician.

Power cord is not plugged into the power entry module, or power cord is not plugged into an appropriately grounded outlet.

Make sure the power cord is plugged into the power entry module of the pressure infusor. Make sure the pressure infusor is plugged into a properly grounded outlet.

Unit is not turned ON.

Using the main power switch located under the pressure infusor turn the unit ON.

Burned out LED light(s).

Contact a biomedical technician.

Unit failure.

Contact a biomedical technician.

Blown fuse.

Contact a biomedical technician.

12

Troubleshooting

Ranger™ Pressure Infusor Model 145

Pressure infusor

Ranger™ Pressure Infusor Model 145

Cause

Solution

Pressure infusor is not working.

Power cord is not plugged into the power entry module, or power cord is not plugged into an appropriately grounded outlet.

Make sure the power cord is plugged into the power entry module of the pressure infusor. Make sure the pressure infusor is plugged into a properly grounded outlet.

Unit is not turned ON.

Using the main power switch located under the pressure infusor turn the unit ON.

Unit fault.

Discontinue use of unit. Contact a biomedical technician.

Blown fuse.

Contact a biomedical technician.

Pressure infusor bladder is loose or has become unattached.

• Discontinue use of pressure infusor chamber. Use the other side of the pressure infusor

Cleaning the pressure infusor and cord

• Reattach bladder by using your thumbs to fit one side of the bladder port on the bladder retaining collar and stretch into position.

1. 2.

High indicator (solid yellow visual with audible indicator).

13

Section 5: Maintenance and Storage

Condition

Low indicator (solid yellow visual with audible indicator).

Maintenance and Storage

Pressure infusor door may not be closed and securely latched.

Securely close and latch the pressure infusor door.

Detected pressure has fallen below 230 mmHg.

Continue infusion or use the other side of the pressure infusor. Contact a biomedical technician after use.

Pressure is above 330 mmHg.

Discontinue use of pressure infusor chamber. Use the other side of the pressure infusor. Contact a biomedical technician after use.

Leakage of fluid.

Bag is not spiked securely.

Secure spike in bag.

Bladder does not deflate after pressure is discontinued.

Unit fault.

Contact a biomedical technician after use.

Cleaning the Ranger pressure infusor Clean the Ranger pressure infusor on an as-needed basis or per institutional protocol.

NOTICE: • Do not immerse the pressure infusor or use a dripping wet cloth for cleaning. Moisture may seep inside the device and damage the electrical components. Clean the pressure infusor exterior with a soft cloth using plain water or a mild, all-purpose or nonabrasive cleaner. • Do not spray cleaning solutions onto the pressure infusor. Damage to the pressure infusor may occur.

Clean the Ranger pressure infusor on an as-needed basis or per facility policies and procedures for cleaning electronic equipment.

3.

Disconnect power supply from power outlet. Use a slightly damp soft cloth moistened with a mild, nonabrasive cleaning solution to clean the device surfaces, hose, and cord. Avoid getting liquid into electronic ports. Dry with a separate soft cloth.

Storage Cover and store all components in a cool, dry place when not in use. Take care not to drop or jar the unit.

English

34-8719-2475-8

12

Troubleshooting

Ranger™ Pressure Infusor Model 145

Pressure infusor

Ranger™ Pressure Infusor Model 145

Cause

Solution

Pressure infusor is not working.

Power cord is not plugged into the power entry module, or power cord is not plugged into an appropriately grounded outlet.

Make sure the power cord is plugged into the power entry module of the pressure infusor. Make sure the pressure infusor is plugged into a properly grounded outlet.

Unit is not turned ON.

Using the main power switch located under the pressure infusor turn the unit ON.

Unit fault.

Discontinue use of unit. Contact a biomedical technician.

Blown fuse.

Contact a biomedical technician.

Pressure infusor bladder is loose or has become unattached.

• Discontinue use of pressure infusor chamber. Use the other side of the pressure infusor

Cleaning the pressure infusor and cord

• Reattach bladder by using your thumbs to fit one side of the bladder port on the bladder retaining collar and stretch into position.

1. 2.

High indicator (solid yellow visual with audible indicator).

13

Section 5: Maintenance and Storage

Condition

Low indicator (solid yellow visual with audible indicator).

Maintenance and Storage

Pressure infusor door may not be closed and securely latched.

Securely close and latch the pressure infusor door.

Detected pressure has fallen below 230 mmHg.

Continue infusion or use the other side of the pressure infusor. Contact a biomedical technician after use.

Pressure is above 330 mmHg.

Discontinue use of pressure infusor chamber. Use the other side of the pressure infusor. Contact a biomedical technician after use.

Leakage of fluid.

Bag is not spiked securely.

Secure spike in bag.

Bladder does not deflate after pressure is discontinued.

Unit fault.

Contact a biomedical technician after use.

Cleaning the Ranger pressure infusor Clean the Ranger pressure infusor on an as-needed basis or per institutional protocol.

NOTICE: • Do not immerse the pressure infusor or use a dripping wet cloth for cleaning. Moisture may seep inside the device and damage the electrical components. Clean the pressure infusor exterior with a soft cloth using plain water or a mild, all-purpose or nonabrasive cleaner. • Do not spray cleaning solutions onto the pressure infusor. Damage to the pressure infusor may occur.

Clean the Ranger pressure infusor on an as-needed basis or per facility policies and procedures for cleaning electronic equipment.

3.

Disconnect power supply from power outlet. Use a slightly damp soft cloth moistened with a mild, nonabrasive cleaning solution to clean the device surfaces, hose, and cord. Avoid getting liquid into electronic ports. Dry with a separate soft cloth.

Storage Cover and store all components in a cool, dry place when not in use. Take care not to drop or jar the unit.

English

34-8719-2475-8

14

Specifications

Ranger™ Pressure Infusor Model 145

Section 6: Specifications

GUIDANCE AND MANUFACTURER’S DECLARATION – ELECTROMAGNETIC IMMUNITY The model 145 is intended for use in the electromagnetic environment specified below. The customer or the user of the model 145 should assure that it is used in such an environment.

GUIDANCE AND MANUFACTURER’S DECLARATION – ELECTROMAGNETIC EMISSIONS The model 145 is intended for use in the electromagnetic environment specified below. The customer or the user of the model 145 should assure that it is used in such an environment. EMISSIONS TEST

COMPLIANCE

RF emissions CISPR 11

Group 1

The model 145 uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.

RF emissions CISPR 11

Class B

Harmonic emissions IEC 61000-3-2

Class A

The model 145 is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.

Voltage fluctuations/Flicker emissions IEC 61000-3-3

Complies

IMMUNITY TEST

COMPLIANCE LEVEL

ELECTROMAGNETIC ENVIRONMENT - GUIDANCE

Conducted RF IEC 61000-4-6

3 Vrms 150 kHz to 80 MHz

Radiated RF IEC 61000-4-3

3 V/m 80 MHz to 2,5 GHz

GUIDANCE AND MANUFACTURER’S DECLARATION – ELECTROMAGNETIC IMMUNITY The model 145 is intended for use in the electromagnetic environment specified below. The customer or the user of the model 145 should assure that it is used in such an environment. IMMUNITY TEST

IEC 60601 TEST LEVEL

IEC 60601

COMPLIANCE

TEST LEVEL

LEVEL

Electrostatic discharge (ESD) IEC 61000-4-2

±6 kV contact ±8 kV air

±6 kV contact ±8 kV air

Electrical fast transient/ burst IEC 61000-4-4

±2 kV power lines

±2 kV power lines

Mains power quality should be that of a typical commercial or hospital environment.

Surge IEC 61000-4-5

±1 kV line to line ±2 kV line to gnd

±1 kV line to line ±2 kV line to gnd

Mains power quality should be that of a typical commercial or hospital environment.

Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11

<5% UT (>95% dip in UT) for 0,5 cycle 40% UT (60% dip in UT) for 6 cycles 70% UT (30% dip in UT) for 30 cycles <5% UT (>95% dip in UT) for 5 sec

<5% UT (>95% dip in UT) for 0,5 cycle 40% UT (60% dip in UT) for 6 cycles 70% UT (30% dip in UT) for 30 cycles <5% UT (>95% dip in UT) for 5 sec

Mains power quality should be that of a typical commercial or hospital environment. If the user of the model 145 requires continued operation during power mains interruptions, it is recommended that the model 145 be powered from an uninterruptible power supply or a battery.

Power frequency (50/60 Hz) magnetic field IEC 61000-4-8

3 A/m

3 A/m

Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

3 Vrms 3 V/m

ELECTROMAGNETIC ENVIRONMENT - GUIDANCE Portable and mobile RF communications equipment should be used no closer to any part of the model 145, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distance d = 1.2 √P d = 1.2 √P 80 MHz to 800 MHz d = 2.3 √P 800 MHz to 2,5 GHz where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey,a should be less than the compliance level in each frequency range.b Interference may occur in the vicinity of equipment marked with the following symbol:

ELECTROMAGNETIC ENVIRONMENT - GUIDANCE Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.

NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. a

NOTE UT is the a.c. mains voltage prior to application of the test level.

b

Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the model 145 is used exceeds the applicable RF compliance level above, the model 145 should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the model 145. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

14

Specifications

Ranger™ Pressure Infusor Model 145

Section 6: Specifications

GUIDANCE AND MANUFACTURER’S DECLARATION – ELECTROMAGNETIC IMMUNITY The model 145 is intended for use in the electromagnetic environment specified below. The customer or the user of the model 145 should assure that it is used in such an environment.

GUIDANCE AND MANUFACTURER’S DECLARATION – ELECTROMAGNETIC EMISSIONS The model 145 is intended for use in the electromagnetic environment specified below. The customer or the user of the model 145 should assure that it is used in such an environment. EMISSIONS TEST

COMPLIANCE

RF emissions CISPR 11

Group 1

The model 145 uses RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.

RF emissions CISPR 11

Class B

Harmonic emissions IEC 61000-3-2

Class A

The model 145 is suitable for use in all establishments, including domestic establishments and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.

Voltage fluctuations/Flicker emissions IEC 61000-3-3

Complies

IMMUNITY TEST

COMPLIANCE LEVEL

ELECTROMAGNETIC ENVIRONMENT - GUIDANCE

Conducted RF IEC 61000-4-6

3 Vrms 150 kHz to 80 MHz

Radiated RF IEC 61000-4-3

3 V/m 80 MHz to 2,5 GHz

GUIDANCE AND MANUFACTURER’S DECLARATION – ELECTROMAGNETIC IMMUNITY The model 145 is intended for use in the electromagnetic environment specified below. The customer or the user of the model 145 should assure that it is used in such an environment. IMMUNITY TEST

IEC 60601 TEST LEVEL

IEC 60601

COMPLIANCE

TEST LEVEL

LEVEL

Electrostatic discharge (ESD) IEC 61000-4-2

±6 kV contact ±8 kV air

±6 kV contact ±8 kV air

Electrical fast transient/ burst IEC 61000-4-4

±2 kV power lines

±2 kV power lines

Mains power quality should be that of a typical commercial or hospital environment.

Surge IEC 61000-4-5

±1 kV line to line ±2 kV line to gnd

±1 kV line to line ±2 kV line to gnd

Mains power quality should be that of a typical commercial or hospital environment.

Voltage dips, short interruptions and voltage variations on power supply input lines IEC 61000-4-11

<5% UT (>95% dip in UT) for 0,5 cycle 40% UT (60% dip in UT) for 6 cycles 70% UT (30% dip in UT) for 30 cycles <5% UT (>95% dip in UT) for 5 sec

<5% UT (>95% dip in UT) for 0,5 cycle 40% UT (60% dip in UT) for 6 cycles 70% UT (30% dip in UT) for 30 cycles <5% UT (>95% dip in UT) for 5 sec

Mains power quality should be that of a typical commercial or hospital environment. If the user of the model 145 requires continued operation during power mains interruptions, it is recommended that the model 145 be powered from an uninterruptible power supply or a battery.

Power frequency (50/60 Hz) magnetic field IEC 61000-4-8

3 A/m

3 A/m

Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.

3 Vrms 3 V/m

ELECTROMAGNETIC ENVIRONMENT - GUIDANCE Portable and mobile RF communications equipment should be used no closer to any part of the model 145, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter. Recommended separation distance d = 1.2 √P d = 1.2 √P 80 MHz to 800 MHz d = 2.3 √P 800 MHz to 2,5 GHz where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site survey,a should be less than the compliance level in each frequency range.b Interference may occur in the vicinity of equipment marked with the following symbol:

ELECTROMAGNETIC ENVIRONMENT - GUIDANCE Floors should be wood, concrete or ceramic tile. If floors are covered with synthetic material, the relative humidity should be at least 30%.

NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people. a

NOTE UT is the a.c. mains voltage prior to application of the test level.

b

Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the model 145 is used exceeds the applicable RF compliance level above, the model 145 should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as re-orienting or relocating the model 145. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

16

Specifications

Ranger™ Pressure Infusor Model 145

Ranger™ Pressure Infusor Model 145

RECOMMENDED SEPARATION DISTANCES BETWEEN PORTABLE AND MOBILE RF COMMUNICATIONS EQUIPMENT AND THE MODEL 145

Electrical characteristics

The model 145 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the model 145 can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the model 145 as recommended below, according to the maximum output power of the communications equipment.

Leakage current

POWER OF TRANSMITTER

17

Meets leakage current requirements in accordance with AAMI 60601-1 and IEC 60601-1.

Power cord 15 feet (4.6 m)

SEPARATION DISTANCE ACCORDING TO FREQUENCY OF TRANSMITTER m

RATED MAXIMUM OUTPUT

Specifications

W

150 KHZ TO 80 MHZ d = 1.2 √P

80 MHZ TO 800 MHZ d = 1.2 √P

800 MHZ TO 2,5 GHZ d = 2.3 √P

0,01

0.12

0.12

0.23

0,1

0.37

0.37

0.74

1

1.17

1.17

2.30

10

3.69

3.69

7.37

100

11.67

11.67

23.30

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

Physical characteristics Dimensions 15.75 in (40 cm) high 20 in (51 cm) wide, 7.75 in (20 cm) deep

Device rating 110-120 VAC, 50/60 Hz, 1 Amp 220-240 VAC, 50/60 Hz, 0.8 Amp

Fuse 2 x F1A-H, rated 250V, for 110-120 VAC unit 2 x F0.8A-H, rated 250V, for 220-240 VAC unit

Storage and transport conditions Storage/transport temperature -20 to 60˚C (-4˚F to 140˚F) Store all components at room temperature and in a dry place when in use.

Operating humidity Up to 90% RH, noncondensing

Atmospheric pressure range Altitude up to 2000m or 80 kPa

Performance characteristics Operating pressure

Weight

300 mmHg setpoint

17 lb. (7.7 kg)

Note:

Mounting

• Pressure system is In Range when the pressure infusor bladders are inflated to between 230 mmHg (low) and 330 mmHg (high). If pressure falls below 230 mmHg for more than approximately 30 seconds the Low yellow indicator will illuminate and an audible indicator will sound. The High yellow and audible indicator notifies the user when the pressure infusor bladder is above 330 mmHg.

Dual clamp

Classification Classified under IEC 60601-1 Guidelines as Class 1, Type BF, Ordinary Equipment.

• The outlet pressure of the fluid may vary with the surface area and volume of the fluid bag.

Medical Equipment 4HZ8

MEDICAL - GENERAL MEDICAL EQUIPMENT AS TO ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH UL 60601-1; CAN/CSA-C22.2, No.601.1; ANSI/AAMI ES60601-1:2005 CSA-C22.2 No. 60601-1:08; Control No.4HZ8 Classified under IEC 60601-1 Guidelines (and other national versions of the Guidelines) as Class I, Type BF, defibrillation proof, IPX1 rated, Ordinary equipment, Continuous operation. Classified by Underwriters Laboratories Inc. with respect to electric shock, fire and mechanical hazards only, in accordance with IEC/EN 60601-1 and in accordance with Canadian/CSA C22.2, No. 601.1. Classified under the Medical Device Directive as a Class IIb device.

English

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16

Specifications

Ranger™ Pressure Infusor Model 145

Ranger™ Pressure Infusor Model 145

RECOMMENDED SEPARATION DISTANCES BETWEEN PORTABLE AND MOBILE RF COMMUNICATIONS EQUIPMENT AND THE MODEL 145

Electrical characteristics

The model 145 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the model 145 can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the model 145 as recommended below, according to the maximum output power of the communications equipment.

Leakage current

POWER OF TRANSMITTER

17

Meets leakage current requirements in accordance with AAMI 60601-1 and IEC 60601-1.

Power cord 15 feet (4.6 m)

SEPARATION DISTANCE ACCORDING TO FREQUENCY OF TRANSMITTER m

RATED MAXIMUM OUTPUT

Specifications

W

150 KHZ TO 80 MHZ d = 1.2 √P

80 MHZ TO 800 MHZ d = 1.2 √P

800 MHZ TO 2,5 GHZ d = 2.3 √P

0,01

0.12

0.12

0.23

0,1

0.37

0.37

0.74

1

1.17

1.17

2.30

10

3.69

3.69

7.37

100

11.67

11.67

23.30

For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer. NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies. NOTE 2 These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects and people.

Physical characteristics Dimensions 15.75 in (40 cm) high 20 in (51 cm) wide, 7.75 in (20 cm) deep

Device rating 110-120 VAC, 50/60 Hz, 1 Amp 220-240 VAC, 50/60 Hz, 0.8 Amp

Fuse 2 x F1A-H, rated 250V, for 110-120 VAC unit 2 x F0.8A-H, rated 250V, for 220-240 VAC unit

Storage and transport conditions Storage/transport temperature -20 to 60˚C (-4˚F to 140˚F) Store all components at room temperature and in a dry place when in use.

Operating humidity Up to 90% RH, noncondensing

Atmospheric pressure range Altitude up to 2000m or 80 kPa

Performance characteristics Operating pressure

Weight

300 mmHg setpoint

17 lb. (7.7 kg)

Note:

Mounting

• Pressure system is In Range when the pressure infusor bladders are inflated to between 230 mmHg (low) and 330 mmHg (high). If pressure falls below 230 mmHg for more than approximately 30 seconds the Low yellow indicator will illuminate and an audible indicator will sound. The High yellow and audible indicator notifies the user when the pressure infusor bladder is above 330 mmHg.

Dual clamp

Classification Classified under IEC 60601-1 Guidelines as Class 1, Type BF, Ordinary Equipment.

• The outlet pressure of the fluid may vary with the surface area and volume of the fluid bag.

Medical Equipment 4HZ8

MEDICAL - GENERAL MEDICAL EQUIPMENT AS TO ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH UL 60601-1; CAN/CSA-C22.2, No.601.1; ANSI/AAMI ES60601-1:2005 CSA-C22.2 No. 60601-1:08; Control No.4HZ8 Classified under IEC 60601-1 Guidelines (and other national versions of the Guidelines) as Class I, Type BF, defibrillation proof, IPX1 rated, Ordinary equipment, Continuous operation. Classified by Underwriters Laboratories Inc. with respect to electric shock, fire and mechanical hazards only, in accordance with IEC/EN 60601-1 and in accordance with Canadian/CSA C22.2, No. 601.1. Classified under the Medical Device Directive as a Class IIb device.

English

34-8719-2475-8