Accutorr V Operating Instructions Feb 2018

Operating Instructions

0070-02-0699-02_Acctr V ops b_w.indd 1

2/18/11 9:21 AM

Accutorr® is a registered trademark of Mindray DS USA, Inc. Masimo SET® is a U.S. registered trademark of Masimo Corp. Mindray® is a trademark or a registered trademark of Shenzhen Mindray Bio-Medical Electronics Co., Ltd. Nellcor® is a U.S. registered trademark of Nellcor Puritan Bennett LLC. SmarTemp™ is a trademark of Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Copyright © Mindray DS USA, Inc., 2009. All rights reserved. Contents of this publication may not be reproduced in any form without permission of Mindray DS USA, Inc.

0070-10-0699-02

Accutorr V Operating Instructions

Table of Contents

Foreword ... v Warnings, Cautions, and Notes... vi Warnings... vi Cautions ... vii Notes ... ix Safety Designations ... ix Indications For Use ... x Product Limitations... x Unpacking... xi Symbols and Descriptions... xi General Description ... 1 - 1 General Product Description ...1 - 2 Product Features...1 - 4 Recommended Test and Calibration Frequency ...1 - 5 Controls and Indicators ... 2 - 1 Introduction ...2 - 2 Front Panel ...2 - 3 Rear Panel...2 - 7 Recorder Module ...2 - 8 Operation... 3 - 1 Introduction ...3 - 2 Operator Position ...3 - 2 Setting-up and Turning Power On ...3 - 2 Standby and Power OFF ...3 - 4 Entering Standby ...3 - 4 Exiting Standby ...3 - 4 Turning Power Off...3 - 4 Selecting a Configuration ...3 - 4 Patient Setup...3 - 6 Entering Patient Information...3 - 6 Quick Admit ...3 - 7 Selecting the Patient Size ...3 - 7 Setting Initial Cuff Inflation Pressure...3 - 8 Manual NIBP Measurements ...3 - 11 NIBP Pressure Limit Fail Safe ...3 - 13 Cuff Inflation Time...3 - 13 Automatic Retry ...3 - 13 Automatic NIBP Measurements (Interval Mode) ...3 - 14 Starting an Automatic Measurement ...3 - 14 Canceling an Automatic NIBP Measurement ...3 - 14 Changing the Interval Setting ... 3 - 15 START and DEFLATE Functions...3 - 15 Automatic Adjustment of Cuff Inflation Pressure (Adaptive Inflation) ...3 - 15 Automatic Retry ...3 - 16 Alarms ...3 - 17

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Table of Contents

Setting Alarm Limits...3 - 17 Alarm Violations ...3 - 19 Pausing and Silencing Alarms ...3 - 20 Viewing and Deleting Stored Trend Data... 3 - 21 Storing Measurements ...3 - 21 Viewing Stored/Trend Data ...3 - 21 Reviewing and Deleting Stored/Trend Data ...3 - 22 Selecting a Patient ID ...3 - 22 Reviewing Trend Data ...3 - 22 Deleting Trend Data ...3 - 23 Exiting the REVIEW SETUP Dialog ...3 - 23 Common Setup ...3 - 24 Setting the Alarm Volume, Key Volume, and Pulse Volume, and NIBP End Tone Volume ...3 - 24 Setting the LCD Brightness and Contrast...3 - 24 SpO2 Measurements ...3 - 26 Pulse Oximetry Sensors...3 - 26 Sequence for Establishing SpO2 with Nellcor® Pulse Oximetry ...3 - 28 NELLCOR® Sensors ...3 - 29 Sequence for Establishing SpO2 with Masimo® Pulse Oximetry ...3 - 29 MASIMO® Sensors and Patient Cable ...3 - 31 DPM SpO2 ...3 - 31 Temperature Measurement ...3 - 34 Setting Temperature Properties ...3 - 34 Applying a Probe Cover (SmarTemp) ...3 - 35 Taking an Oral Temperature Measurement ...3 - 35 Taking an Axillary Temperature Measurement ...3 - 36 Measuring Rectal Temperature ...3 - 37 Recorder ...3 - 39 Setting The Clock (Date and Time) ...3 - 40 Battery Operation...3 - 41 Creating a User Configuration ...3 - 42 Turning Barcode Power On or Off ...3 - 43 Selecting a Language ...3 - 43 Turning Alarm Tones Off...3 - 44 SpO2 Sensor Off ...3 - 44 Saving a user configuration ...3 - 44 Setting a Default Power-on Configuration ...3 - 45 Status and Error Codes ...3 - 47 Physiological Alarm Messages ...3 - 47 Technical Alarm Messages...3 - 47 General Alarm Messages of Parameter Modules...3 - 48 NIBP Module Alarm Messages ...3 - 48 Masimo SpO2 Module Alarm Messages...3 - 50 Nellcor SpO2 Module Alarm Messages...3 - 51 DPM SpO2 Module Alarm Messages ...3 - 51 SmarTemp™ TEMP Module Alarm Messages ...3 - 53 Recorder Module Alarm Messages...3 - 53

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Accutorr V Operating Instructions

Table of Contents

System Alarm Messages ...3 - 55 Prompt Messages...3 - 55 User Maintenance ... 4 - 1 Introduction ...4 - 2 Cleaning and Disinfection of the Accutorr V Monitor...4 - 3 Decontamination of the Optional SmarTemp™ TEMP Probe ...4 - 4 Sterilization and Cleaning of Reusable Cuffs...4 - 5 Battery Maintenance and Replacement ...4 - 6 Battery Maintenance ...4 - 6 Battery Replacement...4 - 6 Recorder Maintenance ...4 - 7 Recorder Paper Replacement...4 - 7 Care and Storage of Thermal Paper ...4 - 9 Resetting the NIBP ...4 - 10 Nurse Call Set-up ...4 - 12 Accutorr V Accessories ... 5 - 1 Accessories ...5 - 2 Hoses, Non Invasive Blood Pressure ...5 - 2 Oximetry Sensors and Accessories...5 - 3 Pulse Oximetry DPM SpO2 ...5 - 3 Pulse Oximetry-Masimo SET® LNOP® SpO2 ...5 - 4 Pulse Oximetry-Masimo SET® LNCS® SpO2 ...5 - 5 Pulse Oximetry-Nellcor® SpO2 ...5 - 5 SmarTemp Temperature Accessories...5 - 5 Welch Allyn SureTemp® Plus Thermometer Accessories ...5 - 6 Nurse Call Connector...5 - 6 Recorder Paper...5 - 6 Barcode Scanner ...5 - 6 Battery and Power Cords ... 5 - 6 Mounting Assemblies ...5 - 6 Appendix ... 6 - 1 How To Get Assistance ...6 - 2 Specifications ...6 - 3 Systolic Pressure Readout ...6 - 3 Diastolic Pressure Readout ...6 - 3 Mean Pressure Readout ... 6 - 3 NIBP Measurement Cycle Time ...6 - 3 Pulse Rate ...6 - 4 Maximum Cuff Pressure ...6 - 4 Temperature...6 - 5 Nellcor® Performance Specifications ...6 - 5 Masimo Performance Specifications ...6 - 6 DPM Performance Specifications...6 - 8 Battery...6 - 8 Real Time Clock...6 - 10 Physical Characteristics ...6 - 10

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Recovery from Power Loss ...6 - 11 Alarm Restoration from Power Loss ...6 - 11 Data Logging after Power Loss ...6 - 11 Environmental Characteristics ...6 - 12 Electrical Ratings...6 - 13 Agency Compliance ...6 - 14 Electromagnetic Compatibility...6 - 15 Indirect Blood Pressure Measurements and Associated Errors...6 - 19 Precautions With Using Automatically Cycled Blood Pressure Cuffs ...6 - 20 Cuff Size ...6 - 20 Other Factors ...6 - 20 User Verification Of The Accutorr V NIBP Measurements...6 - 21 Warranty ...6 - 22 Manufacturer’s Responsibility ...6 - 23

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Accutorr V Operating Instructions

Foreword

Introduction

Foreword These operating instructions are intended to provide information for the proper operation of the Mindray DS USA, Inc. Accutorr V. The Accutorr V configurations are: • Accutorr V with Nellcor® Pulse Oximetry- includes NIBP, Nellcor SpO2, a Trend Display, and Recorder • Accutorr V with Nellcor® Pulse Oximetry and SmarTemp™- includes NIBP, Nellcor SpO2, SmarTemp, a Trend Display, and Recorder • Accutorr V with Masimo SET® Pulse Oximetry- includes NIBP, Masimo SpO2, a Trend Display, and Recorder • Accutorr V with Masimo SET® Pulse Oximetry and SmarTemp™- includes NIBP, Masimo SpO2, SmarTemp, a Trend Display, and Recorder • Accutorr V with DPM Pulse Oximetry- includes NIBP, DPM SpO2, a Liquid Crystal Display (LCD), and Recorder • Accutorr V with DPM Pulse Oximetry and SmarTemp™- includes NIBP, DPM SpO2, SmarTemp, a Liquid Crystal Display (LCD), and Recorder • Accutorr V with DPM NIBP and SmarTemp™- includes NIBP, SmarTemp, a Trend Display, and Recorder • Accutorr V with DPM NIBP only- includes NIBP, a Trend Display, and Recorder All Accutorr V configurations can be upgraded with a barcode scanner. In this manual, when a described feature refers to a particular Accutorr V configuration, it will be noted. When the name Accutorr V is used, it refers to all configurations. General knowledge of monitoring and an understanding of the features and functions of the Accutorr V are prerequisites for its proper use. DO NOT OPERATE THIS UNIT BEFORE READING ALL INSTRUCTIONS. Refer to the Accutorr V Service Manual: P/N 0070-00-0702 for information for servicing this instrument. For additional information or assistance, contact an authorized representative. 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. 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. 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 express or implied license to use the device with replacement parts which 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, Cautions, and Notes

Nellcor Patents: This device (Nellcor SpO2 Module) is covered under one or more of the following U.S. Patents Patent No. 5,485,847, 5,676,141, 5,743,263, 6,035,223, 6,226,539, 6,411,833, 6,463,310, 6,591,123, 6,708,049, 7,016,715, 7,039,538, 7,120,479, 7,120,480, 7,142,142, 7,162,288, 7,190,985, 7,194,293, 7,209,774, 7,212,847, and 7,400,919. Possession or purchase of this device does not convey any express or implied license to use the device with replacement parts which would, alone, or in combination with this device, fall within the scope of one or more of the patents relating to this device.

Warnings, Cautions, and Notes Read and adhere to all of the warnings and cautions 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.

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: Continued use of the STAT NIBP mode or short term automatic mode may result in surface vessel rupture (petechia). WARNING: Always place the unit on a flat, rigid surface or onto a Mindray approved stable mounting bracket. WARNING: To ensure proper performance and safety and to prevent the voiding of the warranty, only use authorized parts and accessories with the Accutorr V. Use of unauthorized accessories may result in erroneous readings. WARNING: Use only cuffs with approved quick connect type connectors. WARNING: The Accutorr V is not intended for use in a magnetic resonance imaging (MRI) environment and may interfere with MRI procedures.

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Cautions

Introduction

WARNING: Danger of explosion if battery is incorrectly replaced. Replace only with the same or equivalent type recommended by the manufacturer. Dispose of used batteries according to the manufacturers instructions and local regulations. Batteries used in this device may present a risk of fire or chemical burn if mistreated. Do not incinerate battery, possible explosion may occur. WARNING: Do not use a damaged or broken unit or accessory. WARNING: Operation of the Accutorr V 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 V. It can also cause delayed recovery after the discharge of a cardiac defibrillator. WARNING: Perform the decontamination or cleaning process with the unit powered down and power cord removed. WARNING: Use only authorized single use disposable probe covers when taking temperature measurements. Use of any other probe cover may result in erroneous readings or damage to the probe.

Cautions CAUTION:

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. The Accutorr V should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the Accutorr V should be observed to verify normal operation in the configuration in which it will be used.

CAUTION:

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

CAUTION:

At the end of their life, dispose of the Accutorr V, accessories, and single use supplies in accordance with local regulations. Dispose of packaging waste in accordance with local regulations.

CAUTION:

Wrapping the cuffs too tightly may cause a hazard to the patient.

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:

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

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Introduction

viii

Cautions

CAUTION:

When equipped with DPM SpO2, use only DPM oxygen sensors and cables. Use of other oxygen sensors may cause improper oximeter performance.

CAUTION:

Excessive ambient light may cause inaccurate SpO2 measurements. Cover the sensor with opaque materials.

CAUTION:

Inaccurate readings 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 or 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:

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. If the sensor or patient cable is damaged in any way, discontinue use immediately.

CAUTION:

When cleaning sensors, do not use excessive amounts of liquid. Wipe the sensor surface with a soft cloth, dampened with the cleaning solution. To prevent damage, do not soak or immerse the sensor in any liquid solution. DO NOT ATTEMPT TO STERILIZE.

CAUTION:

Prolonged and continuous monitoring may increase the risk of skin erosion and pressure necrosis at the site of the sensor. Check the SpO2 sensor site frequently to ensure proper positioning, alignment, and skin integrity at least every eight (8) hours; with the Adult and Pediatric re-usable finger sensor, check every four (4) hours; for neonates and patients of poor perfusion or with skin sensitive to light, check every 2 - 3 hours; more frequent examinations may be required for different patients. Change the sensor site if signs of circulatory compromise occur. Ensure proper adhesion, skin integrity, and proper alignment. Exercise extreme caution with poorly perfused patients. When sensors are not frequently monitored, skin erosion and pressure necrosis can occur. Assess the site every two (2) hours with poorly perfused patients and neonates.

CAUTION:

Recharge the Lithium ion battery while in the unit at room temperature. If using the Accutorr V in a hot environment, the Lithium ion battery may not charge when the unit is connected to the AC mains.

CAUTION:

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

CAUTION:

The Communications Connectors on the Accutorr V are only for use with IEC 60601-1-1 compliant equipment.

CAUTION:

Never place fluids on top of this monitor. If fluid spills on the unit, wipe clean immediately and refer the unit to qualified service personnel.

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Accutorr V Operating Instructions

Notes

Introduction

Notes NOTE:

The Accutorr V should be operated only by trained and qualified personnel.

NOTE:

Use disposable and single use accessories only once.

NOTE:

Place the equipment in a location where the screen can easily be seen and the operating controls can easily be accessed.

NOTE:

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.

NOTE:

The instructions in this manual are based on the maximum configuration.

NOTE:

The optional Temperature module kit must be installed only by trained personnel, and proper ESD prevention methods must be followed.

NOTE:

Only devices specified by Mindray DS USA, Inc. shall be connected the RS-232 port

NOTE:

When the RS-232 connector is used for DIAP, barcode power must be set to OFF.

NOTE:

Disconnect the Accutorr V from the mains to isolate it from the mains power during an emergency.

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. Temp - Type BF protected applied part.

Supply Connection

100 – 240 VAC 50/60 Hz 0.85 – 0.5 A

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Introduction

Indications For Use

Mode of Operation

Continuous

Protection Against Hazard of Explosion

Not Protected (Ordinary)

Protection Against Ingress of Liquids

IPX1

Degree of Electrical Connection Between

Equipment designed for direct electrical and

Equipment and Patient

non-electrical connection to the patient.

Degree of Mobility

Portable

Indications For Use The Accutorr V is intended for intra-hospital use under the direct supervision of a licensed healthcare practitioner. The Indications for Use for the Accutorr V include the monitoring of the following human physiological parameters: • Noninvasive blood pressure (NIBP) • Pulse oximetry (SpO2) • Heart Rate • Temperature

Product Limitations Non-invasive blood pressure (NIBP) accuracy depends on the application of the proper cuff size. See Chapter 3.0 for detailed information. The Accutorr V will not operate effectively on patients who are experiencing convulsions or tremors. The Accutorr V 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 V is computed from the measurement of peripheral pulses (peripheral pulses taken only during a measurement cycle). The rate measured by the Accutorr V 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 vasoconstrictor drugs (for example, norepinephrine), may reduce peripheral perfusion to a level that prevents the Accutorr V from taking pulse rate measurements. Arterial compression, tricuspid regurgitation, or other conditions may reduce perfusion to a level that prevents the Accutorr V from taking pulse rate measurements. The presence of arrhythmias may increase the time required to complete a measurement and may extend this time so that a measurement cannot complete.

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Accutorr V Operating Instructions

Unpacking

Introduction

The Accutorr V is not intended for use during CPR. The monitor uses an oscillometric technique based on normal peripheral circulation to compute blood pressure.

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 or (201) 265-8800 for prompt assistance in resolving shipping problems. NOTE:

The Accutorr V should only be shipped in its original packing materials to avoid shipping damage.

Symbols and Descriptions SYMBOL

DESCRIPTION

SYMBOL

DESCRIPTION

Attention, Consult Accompanying Documents /

Type BF Equipment

Refer to Manual

T1 SpO2

Equipotentiality

Defibrillator-proof Type BF

Equipotential grounding

Equipment

Alternating Current (AC)

Adult

Predictive Thermometer Connector

Pediatric/Child

SpO2 Connector

Neonate

Operating on battery power

Manufacturer

Connected to AC mains NIBP Connector

Accutorr V Operating Instructions

Power On/Off – Standby

Recycle

Serial number

Up key

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Introduction

Symbols and Descriptions

SYMBOL

REF

DESCRIPTION

SYMBOL

DESCRIPTION

Part Number

Confirm key

Patient Information key

Down key

Main menu key

Deflate Cuff key

Set alarms key

Patient Size key

Start NIBP key

Alarm Silence key

Display Tabular Trends/Pleth Wave

NC1

NIBP interval key

SP1

Print key (front panel)

CS1

Nurse Call connector RS-232 connector (Serial Port 1) Network connector Alarm Disabled indicator on

Print key (recorder)

LCD display

Alarm Silenced indicator on

Audio Alarm Off indicator on

LCD display

LCD display

Classified by Underwriters Laboratories Inc. with respect to electric shock, fire and mechanical hazards, only in accordance with UL 60601-1, CAN/CSA C22.2 NO.601-1, IEC 60601-1-1, IEC 60601-2-30, IEC 60601-2-49.

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Accutorr V Operating Instructions

1.0

General Description

General Product Description ... 1-2 Product Features ... 1-4 Recommended Test and Calibration Frequency... 1-5

Accutorr V Operating Instructions

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General Product Description

1.1

General Description

General Product Description The Accutorr V monitors vital signs non-invasive blood pressure (NIBP), pulse oxygen saturation (SpO2), pulse rate (PR), and temperature (Temp) for a single adult, pediatric, or neonatal patient. Temperature is measured using the optional Temperature Module.

FIGURE 1-1

View of Accutorr V Front Panel

An Accutorr V contains an NIBP module, SpO2 module, a rechargable Lithium ion battery, and an internal printer.

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Accutorr V Operating Instructions

General Description

General Product Description

Product Configurations:

NIBP MODULE

SPO2 MODULE

PREDICTIVE TEMPERATURE MODULE

BATTERY

RECORDER

DPM NIBP

DPM SpO2

-

Lithium ion

Recorder

DPM NIBP

DPM SpO2

SmarTemp™

Lithium ion

Recorder

DPM NIBP

DPM NIBP

Masimo SET® SpO2 (MS-2013) Masimo SET® SpO2 (MS-2013) Nellcor Oximax® SpO2 (NELL-3) Nellcor Oximax® SpO2 (NELL-3)

DPM NIBP

-

SmarTemp™

Lithium ion

Recorder

DPM NIBP

-

-

Lithium ion

Recorder

NOTE:

For any of these configurations, the Barcode Scanner is optional.

DPM NIBP DPM NIBP

-

Lithium ion

Recorder

SmarTemp™

Lithium ion

Recorder

-

Lithium ion

Recorder

SmarTemp™

Lithium ion

Recorder

All configurations measure NIBP, pulse rate, and SpO2 (optional). The Accutorr V features front panel digital displays for Mean Arterial Pressures, Temperature, and Interval Mode Timer. It has extra large displays for the Systolic, Diastolic, Pulse Rate, optional Temperature, and SpO2 with a choice of Nellcor, Masimo, or DPM. The Accutorr V incorporates a Liquid Crystal Display (LCD) to view stored measurements and to access system setting menus. On all units, temperature can be measured with the optional Predictive Thermometer Module (SmarTemp). All units are equipped with a recorder module for documenting NIBP, pulse rate, SpO2, and temperature information. Each printout includes the time and date of each measurement. The Accutorr V stores a maximum of 1,200 groups of measurement data in memory. These 1,200 groups of measurement data are shared by the number of patients that are monitored (one patient at a time) by the Accutorr V. When only one patient is monitored, the Accutorr V can store up to 1,200 groups of measurement data for that one patient. When more than one patient is monitored, the Accutorr V can store any number of measurements for each patient provided the total number of stored groups of measurement data for all patients equals 1,200 or less. The Accutorr V has an Interval Mode that enables the unit to take automatic NIBP measurements at timed intervals. Alarm limits can be set for Accutorr V parameters. All alarm violations are indicated by an audible alarm tone, flashing front panel displays, parenthesis around the violated parameter on the recorder printouts, and reverse video on the Trend display. The Accutorr V can operate from a battery.

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Product Features

1.2

General Description

Product Features Some key features of the Accutorr V are: • Non-Invasive Blood Pressure (NIBP) • Pulse Rate • Nellcor, Masimo, or DPM SpO2 • Alarms • Interval Mode • Large Light Emitting Diode (LED) Displays • Trend Memory-Up to 1,200 Measurements • Communications-Improved ASCII Protocol (DIAP) using straight serial cable • Nurse Call function • Universal Power Supply • User Configured Settings • Optional Predictive Thermometer Module (SmarTemp) • Recorder • High Contrast LCD • Customer Replaceable Lithium ion Battery • Universal mounting adapter for rolling stands and wall mounts • Barcode ready

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Accutorr V Operating Instructions

General Description

1.3

Recommended Test and Calibration Frequency

Recommended Test and Calibration Frequency

CHECK/MAINTENANCE ITEM

FREQUENCY

Visual test

When first installing or after reinstalling.

Power on test

1. When first installing or after reinstalling. 2. Following any maintenance or replacement of any main unit part.

NIBP tests

Accuracy test Leakage test Calibration

1. If the user suspects that the measurement is incorrect. 2. Following any repairs or replacement of the NIBP module. 3. At least once per year.

SpO2 test Temperature test Analog output test

If the user suspects that analog output is abnormal.

Bar code scanner test

If the user suspects that bar code scan is incorrect.

Electrical safety tests

Enclosure leakage current test

1. Following any repair or replacement of the power module. 2. At least once every two years.

Earth leakage current test Patient leakage current test Patient auxiliary current test Recorder check

Accutorr V Operating Instructions

Following any repair or replacement of the recorder.

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