Accutorr PLUS Operators Instructions Rev AC

Operating Instructions

Accutorr® Datascope

Accutorr®

Accutorr Plus™ is a U.S. trademark of Mindray DS USA, Inc. Masimo SET® and LNOP® are registered trademarks of Masimo Corporation. Nellcor®, Oxiband®, and Durasensor® are U.S. registered trademarks of Nellcor Puritan Bennett Inc. Oxisensor™ is a trademark of Nellcor Puritan Bennett Inc. Velcro® is a registered trademark of Velcro Industries B.V.

Copyright © Mindray DS USA, Inc., 2008. All rights reserved. Contents of this publication may not be reproduced in any form without permission of Mindray DS USA, Inc.

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Accutorr Plus™ Operating Instructions

Table of Contents

Foreword ... v Warnings, Precautions and Notes... vi Warnings ... vi Cautions ... viii Safety Designations... xi Product Limitations ... xii Unpacking ... xii Symbols and Descriptions ... xiii

General Description ... 1 - 1 General Description ... 1 - 1

Controls and Indicators ... 2 - 1 Front Panel... 2 - 3 Rear Panel ... 2 - 9 Predictive Thermometer Module (PTM) ... 2 - 10 Recorder Module ... 2 - 11

Operation... 3 - 1 Setting-up / Turning Power On ... 3 - 1 Patient Setup and Room/Bed Assignment... 3 - 3 Selecting the Patient Size... 3 - 3 Cuff Inflation Pressure... 3 - 3 Room Number and Bed Letter ... 3 - 4 Manual NIBP Measurements and General NIBP Measurement Information ... 3 - 5 NIBP Pressure Limit Fail Safe ... 3 - 7 Cuff Inflation Time... 3 - 7 Automatic Adjustment of Cuff Inflation Pressure (Adaptive Inflation)... 3 - 7 Automatic NIBP Measurements (Interval Mode)... 3 - 8 Canceling an Automatic NIBP Measurement ... 3 - 8 Changing the Interval Setting ... 3 - 9 Effects of Changing the Room Number and/or Bed Letter on the Interval Setting... 3 - 9 START and DEFLATE Functions ... 3 - 9 Alarms... 3 - 10 Setting Alarm Limits... 3 - 10 Alarm Violations... 3 - 12 How to Mute Alarms ... 3 - 12 Alarms and Changing the Room Number and/or Bed Letter ... 3 - 12 To View and Delete Stored Data (Trend Mode) ... 3 - 14 To View the Stored Measurements on the Accutorr Plus, basic model ... 3 - 14 To View the Stored Measurements on the Accutorr Plus, advanced models... 3 - 14 To Delete the Stored Measurements on the Accutorr Plus... 3 - 15 Setting the Alarm Volume and Beep Volume... 3 - 16 Setting the LCD Contrast (View Angle Adjustment)... 3 - 17 Display Time Out Mode... 3 - 17 SpO2 Measurements (Accutorr Plus advanced models) ... 3 - 18 Pulse Oximetry Sensors ... 3 - 18 Sequence for establishing SpO2 with Nellcor® Pulse Oximetry... 3 - 20

Sequence for Establishing SpO2 with Masimo® Pulse Oximetry... 3 - 21

Temperature Measurement (Optional)... 3 - 25 Predictive Thermometer Measurements ... 3 - 25 How to Apply the Probe Cover (PTM)... 3 - 25 How to take Oral, Rectal, and Axillary Temperatures ... 3 - 26 Storing Temperature Measurements ... 3 - 28 Recorder (Optional) ... 3 - 29

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Table of Contents

How To Set The Clock (Date and Time)... 3 - 30 Battery Operation ... 3 - 32 User Configuration... 3 - 33 Status and Error Codes... 3 - 36 How to Attach Optional Thermometer and Recorder Modules... 3 - 38 To Attach the Recorder Module: ... 3 - 38 To Attach the Thermometer Module:... 3 - 38 Placement Of The Quick Reference Card ... 3 - 39 Placement of Recorder Paper Loading Label ... 3 - 40

User Maintenance ... 4 - 1 Introduction ... 4 - 1 Care and Cleaning Of Monitor ... 4 - 1 Decontamination of the Accutorr Plus ... 4 - 1 Sterilization and Cleaning of Reusable Cuffs ... 4 - 2 Cleaning Cuffs with Bladders ... 4 - 2 Cleaning Bladderless Cuffs ... 4 - 2 Battery Maintenance and Replacement ... 4 - 4 Battery Maintenance ... 4 - 4 Battery Replacement ... 4 - 5 Recorder Paper Replacement... 4 - 6 To Install Paper... 4 - 6 Thermal Paper Durability ... 4 - 7

Accutorr Plus Versions and Accessories ... 5 - 1 Accutorr Plus Versions ... 5 - 1 Accutorr Plus with Lithium Ion Battery ... 5 - 1 Accutorr Plus with Nellcor® Pulse Oximetry and Lithium Ion Battery... 5 - 1 Accutorr Plus with Masimo SET® Pulse Oximetry and Lithium Ion Battery... 5 - 2 Accessories ... 5 - 3 Hoses, Non Invasive Blood Pressure... 5 - 3 Cuffs, Non Invasive Blood Pressure, Latex Free... 5 - 3 Oximetry Sensors and Accessories... 5 - 5 Recorder Module... 5 - 6 Temperature Modules/Probes ... 5 - 7 Manuals ... 5 - 8 Nurse Call Connector ... 5 - 8 Mounting Assemblies ... 5 - 8 Recorder Paper ... 5 - 8 Battery ... 5 - 9

Appendix ... 6 - 1 Phone Numbers and How To Get Assistance... 6 - 1 Specifications ... 6 - 2 Systolic Pressure Readout... 6 - 2 Diastolic Pressure Readout ... 6 - 2 NIBP Measurement Cycle Time... 6 - 2 Pulse Rate ... 6 - 2 Maximum Cuff Pressure ... 6 - 2 Temperature (Predictive) ... 6 - 3 SpO2 - Nellcor® Performance Specifications ... 6 - 3

SpO2 – Masimo® Performance Specifications ... 6 - 4

Battery ... 6 - 6 Real Time Clock ... 6 - 6 Physical Characteristics ... 6 - 7

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Table of Contents

Environmental Characteristics... 6 - 7 Electrical Ratings ... 6 - 8 Safety Characteristics... 6 - 8 Agency Compliance ... 6 - 9 Electromagnetic Compatibility ... 6 - 10 Indirect Blood Pressure Measurements and Associated Errors ... 6 - 14 Precautions With Using Automatically Cycled Blood Pressure Cuffs ... 6 - 14 Cuff Size ... 6 - 14 Other Factors ... 6 - 14 User Verification Of The Accutorr Plus NIBP Measurements ... 6 - 15 Warranty... 6 - 16 Manufacturer’s Responsibility ... 6 - 16

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Accutorr Plus™ Operating Instructions

Foreword

Introduction

Foreword This operating instructions is intended to provide information for the proper operation of the Accutorr Plus. This manual describes three models-one basic and two advanced-of the Accutorr Plus: 1. Accutorr Plus with Lithium Ion Battery-the Accutorr Plus basic model, which measures non-invasive blood pressure (NIBP) and Pulse Rate 2. Accutorr Plus with Nellcor® Pulse Oximetry and Lithium Ion Battery-the Accutorr Plus advanced model, which includes basic model features, and adds Liquid Crystal Display (LCD), Trend Screen, and SpO2 (Nellcor) 3. Accutorr Plus with Masimo SET® Pulse Oximetry and Lithium Ion Battery-the Accutorr Plus advanced model, which includes basic model features, and adds Liquid Crystal Display (LCD), Trend Screen, and SpO2 (Masimo) In this manual, when a described feature refers to a particular model, it will be noted. When the name Accutorr Plus is used, it refers to all three models. General knowledge of monitoring and an understanding of the features and functions of the Accutorr Plus are prerequisites for its proper use. DO NOT OPERATE THIS UNIT BEFORE READING ALL INSTRUCTIONS. Information for servicing this instrument is contained in the Accutorr Plus Service Manuals: Part Numbers 0070-00-0691 (0998-00-0444-9XX). For additional information or assistance, please contact an authorized representative in your area. U.S. Federal Law restricts this device to sale by or on the order of a physician or other practitioner licensed by state law to use or order the use of this device. NOTE:

In order to ensure proper performance and safety, and to prevent the voiding of the warranty, only approved parts and accessories are to be used with the Accutorr Plus.

NOTE:

Potential hazards due to errors in software or hardware have been minimized by actions taken in accordance with IEC 60601-1-4.

Mindray DS USA, Inc. maintains a policy of continual product improvement and reserves the right to change materials and specifications without notice. Masimo Patents: This device (MASIMO SpO2 Module) is covered under one or more of the following U.S.A. patents: 5,758,644; 5,823,950; 6,011,986; 6,157,850; 6,263,222; 6,501,975; and other applicable patents listed at: www.masimo.com/patents.htm. Possession or purchase of this device does not convey any expressed or implied license to use this device with replacement parts that would, alone or in combination with this device, fall within the scope of one or more of the patents relating to this device.

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Introduction

Warnings, Precautions and Notes

Nellcor Patents: This device (Nellcor SpO2 Module) is covered under one or more of the following U.S.A. patents: 4,802,486; 4,869,254; 4,928,692; 4,934,372; 4,960,126; 5,078,136; 5,485,847; 5,743,263; 5,865,736; 6,035,223; 6,298,252; 6,463,310; 6,591,123; 6,675,031; 6,708,049; 6,801,797; Re.35,122; and non-U.S.A. equivalents. Possession or purchase of this device does not convey any expressed or implied license to use this device with replacement parts that would, alone or in combination with this device, fall within the scope of one or more of the patents relating to this device.

Warnings, Precautions and Notes Please read and adhere to all of the warnings and precautions listed throughout this manual. A WARNING is provided to alert the user to potentially serious outcomes (death, injury or serious adverse events) to the patient or the user. A CAUTION is provided to alert the user that special care should be taken for the safe and effective use of the device. They will include actions to be taken to avoid effects on patients or users that will not be potentially life threatening or result in serious injury, but about which the user should be aware. A NOTE is provided when additional general information is available. Mindray DS USA, Inc. maintains a policy of continual product improvement and reserves the right to change materials and specifications without notice.

Warnings WARNING: Internal Electrical Shock Hazard - This unit does not contain any user-serviceable parts. Do not remove instrument covers. Refer servicing to qualified personnel. When the integrity of the protective earth conductor, in the installation or its arrangement, is in doubt, the equipment should be operated from its internal battery. Observe all CAUTION and WARNING labels on the unit. WARNING: Possible explosion hazard. Do not operate machine near flammable anesthetic agents or other flammable substances. Do not use flammable anesthetic agents (i.e., ether or cyclopropane.) WARNING: Communications Connector - Connection of non-isolated devices to the Communications Connector on this unit may cause chassis leakage to exceed the specification standards. WARNING: Always place the unit on a flat, rigid surface or onto a stable mounting pole. WARNING: Never place fluids on top of this unit. In case of accidental wetting, remove power, dry it immediately and have the unit serviced to insure no hazard exists. WARNING: If fluid spills on the unit or if the unit is damaged, refer to qualified service personnel.

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Accutorr Plus™ Operating Instructions

Warnings

Introduction

WARNING: Observe extreme caution when a defibrillator is in use. Do not touch any part of the patient, table or monitor when a defibrillator is in use. WARNING: Do not leave the patient unattended for long periods of time while using this instrument. WARNING: Use only approved accessories with this product. Use of other accessories may result in erroneous readings. WARNING: This instrument may have trouble obtaining pulse rate and NIBP readings on patients undergoing intra-aortic balloon pump treatment. WARNING: Wrapping the cuffs too tightly may cause a hazard to the patient. WARNING: Only connect cuffs with approved quick connect type connectors. WARNING: The Accutorr Plus is not intended for use in a magnetic resonance imaging (MRI) environment and may interfere with MRI procedures. WARNING: Do not incinerate battery, possible explosion may occur. WARNING: Route cables neatly. Ensure cables, hoses and wires are kept away from patient’s neck to avoid strangulation. Keep floors and walkways free of cables to reduce risk to hospital personnel, patients and visitors. WARNING: Do not use a damaged or broken unit or accessory. WARNING: Do not clean the monitor while it is on and/or plugged in. WARNING: Operation of the Accutorr Plus below the minimum amplitude or value of PATIENT physiological signal may cause inaccurate results. WARNING: Use of ACCESSORIES, transducers and cables other than those specified in the manual may result in increased Electromagnetic Emissions or decreased Electromagnetic Immunity of the Accutorr Plus. It can also cause delayed recovery after the discharge of a cardiac defibrillator. WARNING: The Accutorr Plus should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the Accutorr Plus should be observed to verify normal operation in the configuration in which it will be used. WARNING: Perform the decontamination or cleaning process with the unit powered down and power cord removed. WARNING: When attached to other products ensure that the total chassis leakage currents of all units (combined) do not exceed 300µa. WARNING: Use only authorized accessories. Use of unauthorized accessories may result in erroneous measurements. WARNING: It is essential that a single use disposable probe cover is used when taking temperature measurements.

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Introduction

Cautions

WARNING: Perform this process with the unit powered down and power cord removed.

Cautions

viii

CAUTION:

The unit should be checked periodically for obstructed vents. If an obstruction is found refer to qualified service personnel.

CAUTION:

Operation of the Accutorr Plus below the minimum amplitude or value of patient physiological signal may cause inaccurate results.

CAUTION:

Use of accessories, transducers and cables other than those specified in the manual may result in increased Electromagnetic Emissions or decreased Electromagnetic Immunity of the Accutorr Plus. It can also cause delayed recovery after the discharge of a cardiac defibrillator.

CAUTION:

This battery type may be subject to local regulations regarding disposal. At the end of the battery life dispose of the batteries in accordance with local regulations.

CAUTION:

It is the user’s responsibility, when changing the room/bed, to assure the patient size and alarm settings are set as required.

CAUTION:

Do not place the sensor on an extremity with an invasive catheter or blood pressure cuff in place.

CAUTION:

A pulse oximeter should not be used as an apnea monitor.

CAUTION:

A pulse oximeter should be considered an early warning device. As a trend towards patient deoxygenation is indicated, blood samples should be analyzed by a laboratory co-oximeter to completely understand the patient’s condition.

CAUTION:

Ensure proper routing of the patient cable to avoid entanglement and/or strangulation.

CAUTION:

When equipped with Nellcor® SpO2, use only Nellcor® oxygen transducers including Nellcor® Oxisensor® patient dedicated adhesive sensors. Use of other oxygen transducers may cause improper oximeter performance.

CAUTION:

Tissue damage or inaccurate measurements may be caused by incorrect sensor application or use, such as wrapping it too tightly, applying supplemental tape, failing to inspect the sensor site periodically, or failing to position it appropriately. Carefully read the sensor directions for use, the Accutorr Plus operating instructions, and all precautionary information before use.

CAUTION:

Excessive ambient light may cause inaccurate measurements. Cover the sensor with opaque materials.

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Accutorr Plus™ Operating Instructions

Cautions

Introduction

CAUTION:

Inaccurate reading may be caused by incorrect sensor application or use; significant levels of dysfunctional hemoglobins, (i.e. carbohemoglobins or methemoglobin); or intra-vascular dyes such as indocyanine green methylene blue; exposure to excessive illumination, such as surgical lamps (especially ones with a Xenon light source), bilirubin lamps, fluorescent lights, infrared heating lamps, or direct sunlight; excessive patient movement; venous pulsations; electro-surgical interference; and placement of a sensor on an extremity that has a blood pressure cuff, arterial catheter, or intra-vascular line.

CAUTION:

In certain situations in which perfusion and signal strength are low, such as in patients with thick or pigmented skin, inaccurately low SpO2 readings will result. Verification of oxygenation should be made, especially in preterm infants and patients with chronic lung disease, before instituting any therapy or intervention.

CAUTION:

If the sensor or patient cable is damaged in any way, discontinue use immediately. To prevent damage do not soak or immerse the sensor in any liquid solution. DO NOT ATTEMPT TO STERILIZE.

CAUTION:

When equipped with MASIMO® SpO2, use only MASIMO® oxygen transducers including MASIMO LNOP® patient dedicated adhesive sensors and MASIMO PC Series Patient Cable. Use of other oxygen transducers may cause improper Oximetry performance.

CAUTION:

Many patients suffer from poor peripheral perfusion due to hypothermia, hypovolemia, severe vasoconstriction, reduced cardiac output, etc. These symptoms may cause a loss in vital sign readings.

CAUTION:

The SpO2 sensor site should be checked at least every eight (8) hours (every two (2) hours with the Adult re-usable finger sensor). Ensure proper adhesion, skin integrity, and proper alignment. Exercise extreme caution with poorly perfused patients. Skin erosion and pressure necrosis can be caused when sensors are not frequently monitored. Assess the site every two (2) hours with poorly perfused patients and neonates.

CAUTION:

If the sensor or patient cable is damaged in any way, discontinue use immediately. To prevent damage do not soak or immerse the sensor in any liquid solution. Do not attempt to sterilize.

CAUTION:

Use only authorized probe covers. Use of any other probe cover may result in erroneous readings or damage to the probe.

CAUTION:

Changing any part of the time or date will cause all stored patient information (trend data) to be permanently erased. Viewing the time or date does NOT cause data to be erased.

CAUTION:

To avoid loss of patient data (trend), do not replace the battery unless the Accutorr Plus is connected to an AC receptacle. Hospital defaults and the time are unaffected by battery replacement.

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Introduction

x

Cautions

CAUTION:

It is the users responsibility, when changing the room/bed, to assure the patient size and alarm settings are as required.

CAUTION:

Do not get the detergent into any vent openings.

CAUTION:

Some disinfectants may cause skin irritation. Please rinse cuff thoroughly with water to remove any residual disinfectants.

CAUTION:

Using dark colored soaks may stain the cuffs. Test a single cuff to ensure that no damage will occur.

CAUTION:

When ironing or pressing the cuffs, be aware that the Velcro® fasteners can melt at temperatures above 325°F (162°C).

CAUTION:

Cuffs with bladders contain natural rubber latex which may cause allergic reactions.

CAUTION:

When cleaning sensors do not use excessive amounts of liquid. Wipe the sensor surface with a soft cloth, dampened with the cleaning solution.

CAUTION:

Li-Ion batteries are intended for replacement by qualified service personnel only.

CAUTION:

Batteries used in this device may present a risk of fire or chemical burn if mistreated. Do not disassemble, heat above 100°C (212°F), or incinerate. Replace Lithium Ion battery with P/N: 0146-00-0069 only. Use of another battery may present a risk of fire or explosion.

CAUTION:

Dispose of used battery promptly in accordance with local laws. Keep away from children. Do not disassemble and do not dispose of in fire.

CAUTION:

Recharge the Lithium ion battery while in the unit at room temperature. If the Accutorr Plus is being used in a hot environment, the Lithium Ion battery may not charge when the unit is connected to AC. This safety feature is important because charging a hot battery shortens the battery’s life span.

CAUTION:

Remove the battery if the Accutorr Plus is not likely to be used for an extended period of time.

CAUTION:

The Communications Connector on the Accutorr Plus is only for use with IEC 60601-1 compliant equipment.

CAUTION:

Removing the battery from the Accutorr Plus while the AC line cord is disconnected may cause the alarm settings to be reset to their defaults.

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Accutorr Plus™ Operating Instructions

Safety Designations

Introduction

Safety Designations Safety designations per IEC 60601-1 Standard: Type of protection against electric shock

Class 1 with internal electric power source. Where the integrity of the external protective earth (ground) in the installation or its conductors is in doubt, the equipment shall be operated from its internal electric power source.

Degree of protection against electric shock

Monitor - Type B applied part. NIBP - Type BF defibrillation protected applied part. SpO2 - Type BF protected applied part.

Supply Connection

100-120 VAC / 220-240 VAC 50-60 Hz; 0.85 / 0.5 A 11.1 VDC Lithium Ion Internal Battery

Mode of Operation

Continuous

Protection Against Hazard of Explosion

Not Protected (Ordinary)

Protection Against Ingress of Liquids

Meets the requirements specified by IEC 60601-1, clause 44.3 and IEC 60601-2-30: Non Protected Equipment (IPX1) as specified in EN 60529.

Degree of Electrical Connection Between

Equipment designed for direct electrical and

Equipment and Patient

non-electrical connection to the patient.

Degree of Mobility

Mobile and/or hand held

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Introduction

Product Limitations

Product Limitations Non-invasive blood pressure (NIBP) accuracy depends on the application of the proper cuff size. See Section 3.0 for detailed information. The Accutorr Plus will not operate effectively on patients who are experiencing convulsions or tremors. The Accutorr Plus is a portable device intended for intra-hospital use. If the pressure cuff is not placed at the patient’s heart level, the NIBP measurement may be subject to error, due to the hydrostatic effect. The pulse rate data displayed on the Accutorr Plus is computed from the measurement of peripheral pulses (peripheral pulses taken only during a measurement cycle). The rate measured by the Accutorr Plus may differ from the rate of an ECG monitor. This is because the ECG is an electrical signal that may not always result in a peripheral pulse. Administration of certain vasoconstrictive drugs (for example, norepinephrine), may reduce peripheral perfusion to a level that prevents the Accutorr Plus from taking pulse rate measurements. Arterial compression, tricuspid regurgitation, or other conditions may reduce perfusion to a level that prevents the Accutorr Plus from taking pulse rate measurements. The presence of arrhythmias may increase the time required to complete a measurement and may extend this time to a point where a measurement cannot be completed. The Accutorr Plus is not intended for use during CPR. The monitor uses an oscillometric technique based on normal peripheral circulation to compute blood pressure. On occasion, increased motion, prolonged crying, or hyperactivity may produce measurements with a status code of 8810 (RETRY-UNABLE TO MEASURE) or 8813 (STOPUNABLE TO MEASURE). See section 3.16 for a list of status and error codes.

Unpacking Remove the instrument from the shipping carton and examine it for signs of shipping damage. Save all packing materials, invoice, and bill of lading. These may be required to process a claim with the carrier. Check all materials against the packing list. Contact the Customer Service Department (800) 288-2121 (U.S.A and Canada) or (201) 265-8800 (outside U.S.A. and Canada) for prompt assistance in resolving shipping problems.

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Symbols and Descriptions

Introduction

Symbols and Descriptions Most of the symbols in the table below are defined in the IEC Publication 878 and ISO Standard 7000. These symbols are used on all models of the Accutorr Plus. SYMBOL

DESCRIPTION

SYMBOL

DESCRIPTION

Attention, Consult Accompanying Documents /

Type BF Equipment

Refer to Manual

Cont.

Refer Servicing to Qualified

Defibrillator-proof Type

Service Personnel

BF Equipment

Equipotentiality

Pulse Rate

Alternating Current (AC)

Adult

Direct Current (DC)

Pediatric/Child

Temperature

Neonate

Interval Setting / Timer

Alarm Volume

Continuous NIBP Mode

Beep Volume

Electrical connectors

Battery

Accutorr Plus™ Operating Instructions

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Recycle

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Symbols and Descriptions

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1.0

General Description

1.1

General Description

FIGURE 1-1 Accutorr Plus, advanced model (Historical Trend Display and Oximeter optional features)

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1-1

General Description

General Description

The Accutorr Plus is available in three models-one basic and two advanced: 1. Accutorr Plus with Lithium Ion Battery-the Accutorr Plus basic model, which measures non-invasive blood pressure (NIBP) and Pulse Rate 2. Accutorr Plus with Nellcor® Pulse Oximetry and Lithium Ion Battery-the Accutorr Plus advanced model, which includes basic model features, and adds Liquid Crystal Display (LCD), Trend Screen and SpO2 (Nellcor) 3. Accutorr Plus with Masimo SET® Pulse Oximetry and Lithium Ion Battery-the Accutorr Plus advanced model, which includes basic model features, and adds Liquid Crystal Display (LCD), Trend Screen and SpO2 (Masimo) In this manual, when a feature is described and it only refers to a particular model, it will be noted. When the name Accutorr Plus is used, it refers to all three models. All Accutorr Plus models are supplied with Lithium Ion Battery Technology. All models measure NIBP and pulse rate. The Accutorr Plus features front panel digital displays for Mean Arterial Pressures, Temperature, and Time; and extra large displays for the Systolic, Diastolic, Pulse Rate, and SpO2. The Accutorr Plus advanced models incorporate an LCD to view stored measurements (trend); to access a menu system for setting the alarm volume and SpO2 beep volume; and to display the view angle. Advanced models also add automatic SpO2 measurement function with your choice of Nellcor or Masimo SpO2, depending upon your model. On all units, temperature can be measured with the optional Predictive Thermometer Module (PTM) or the optional AccuTemp IR Infrared Thermometer Module. All units can also be optionally equipped with a recorder module for documenting NIBP, pulse rate, SpO2 and temperature information. Each printout includes the time and date of each measurement taken. The Accutorr Plus can store up to 100 measurements in memory. These 100 measurements are shared by the number of patients that are monitored by the Accutorr Plus. When only one patient is monitored, then that one patient can have up to 100 measurements stored. When more than one patient is monitored each patient can have any number of measurements stored as long as the total number of stored measurements for all patients equals 100 or less. The Accutorr Plus has an Interval Mode which enables the unit to take automatic NIBP measurements at timed intervals. The Accutorr Plus allows setting of alarm limits. All alarm violations are indicated by an audible alarm tone, flashing front panel displays and brackets around the violated parameter on the recorder print outs. The Accutorr Plus also has the capability of operating from a battery.

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General Description

General Description

Some key features of the Accutorr Plus are: • Non-Invasive Blood Pressure (NIBP) • Pulse Rate • Nellcor or Masimo SpO2 (advanced models only) • Alarms • Interval Mode • Large Light Emitting Diode (LED) Displays • Trend Memory - Up to 100 Measurements • Communications - DIAP • Nurse Call function • Universal Power Supply • Automatic Power Saver • User Configured Settings • Thermometry, PTM or AccuTemp IR (Optional) • Recorder (Optional) • High Contrast LCD (advanced models only) • Customer Replaceable Lithium Ion Battery • Universal mounting adapter for rolling stands and wall mounts

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