1 3 SpotOn Temperature Monitoring System Model 370 Installation and Service Manual Please forward to the Biomedical Engineering Department 3M SpotOn Temperature Monitoring System
2 Revision History Revision Reason for Change Pages Affected Date A New Revision - First Release All March 2013
3 Table of Contents A Section 1: Introduction... 3 About this manual... 3 Intended use... 3 Safety information and symbols... 3 Explanation of signal word consequences... 3 Proper use and maintenance... 6 Read before servicing equipment... 6 Description of the SpotOn temperature monitoring system... 7 How it works... 8 Section 2: Installation... 9 Mounting the SpotOn control unit... 9 Section 3: Display Panel Display screens Start-up Standby Ready...12 Equilibration...12 Running...12 Control unit error...12 Sensor error...12 Section 4: Troubleshooting On Mode...13 Displays...13 Errors...14 Section 5: Calibration Verification Stick Calibration verification frequency...15 Method...15 Section 6: General Maintenance...17 Cleaning and disinfecting procedure...17 Cleaning the control unit and sensor cable...17 Disinfecting the sensor cable...17 Storage...17 Service...17 Section 7: Specifications...19 Physical characteristics...19 Electrical characteristics...20 Temperature characteristics...20 Performance characteristics...20 Leakage current...20 Environmental conditions...20
5 Introduction 3 Section 1: Introduction About this manual Intended use Safety information and symbols Explanation of signal word consequences Proper use and maintenance Read before servicing equipment Description of the SpotOn temperature monitoring system How it works About this manual This Installation and Service Manual describes the setup and maintenance of the 3M SpotOn temperature monitoring system. The SpotOn temperature monitoring system is to be used by healthcare professionals in clinical environments only. Read and follow all instructions, labeling and accompanying documents supplied with the SpotOn system. Failure to follow instructions could lead to misuse of the device, device malfunction, or patient injury. Intended use Measure, monitor, and trend body temperature of adult and pediatric patients. Safety information and symbols Date of manufacture Manufacturer Single use only Container quantity 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 A Defibrillation-proof type CF applied part
6 4 Introduction Class II equipment Authorized Representative in the European Community CAUTION: Recycle to avoid environmental contamination This product contains recyclable parts. For information on recycling - please contact your nearest 3M Service Center for advice. Direct current See accompanying documents Consult operator s manual Keep dry Hardware temperature limits Sensor temperature limits Explanation of signal word consequences 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.
7 Introduction A WARNINGS 1. To reduce the risks associated with access to critical patient information or equipment: The SpotOn control unit is to be attached to other equipment by authorized service personnel only. Do not re-install or re-locate the SpotOn control unit. 2. To reduce the risks associated with hazardous voltage, fire, and thermal energy hazards: Use ONLY with 3M SpotOn system components (sensors, cables, and power supply). Do not substitute other devices for the SpotOn control unit, sensor, cables, or power supply. Do not use the SpotOn temperature monitoring system (sensor, control unit, cables, or cords) in an MRI environment. 3. To reduce the risks associated with hazardous voltage and fire: Keep power supply visible and accessible at all times. The plug on the power supply serves as the disconnect device. The power outlet shall be as close as practical and shall be easily accessible. Use only the power supply specified for this product and certified for the country of use. Use only a properly grounded power outlet; do not use extension cords or multiple portable socket outlets. Do not allow the power supply to get wet. Do not use the SpotOn control unit when it appears the unit or system components are damaged. Contact 3M Patient Warming technical support at or Do not service or modify the power supply, control unit, cables, sensor, or any part of the 3M SpotOn system. There are no user serviceable parts. 4. To reduce the risks associated with fire: This system is not suitable for use in the presence of a flammable anesthetic mixture with air nitrous oxide. 5. To reduce the risks associate with pressure, and crushed or entangled cords and connectors: Do not allow the patient to lie on any SpotOn sensor cable or connector. Always position cables and cords away from the patient s body. Do not use a headband or other device to secure the SpotOn sensor to the patient. 6. To reduce the risks associated with incorrect system or sensor use: Limit use of the SpotOn temperature sensor to 24 hours. Extended use may compromise skin, cause degradation of material or performance. Avoid exposing the SpotOn temperature sensor, sensor cable, power supply, and control unit to surgical skin surface preparation solutions or other fluids. Use an additional independent thermometer to measure body temperature during intentional hyperthermia or hypothermia therapy. Confirm unanticipated temperature reading with an independent thermometer, if needed. Do not reposition the SpotOn temperature sensor; repositioning may weaken the sensor adhesive, damage the sensor, or compromise the device performance. Avoid placing the sensor in the center of the forehead as this may affect sensor accuracy. 7. To reduce the risks associated with exposure to biohazards: Follow facilities policies and procedures for disposal of contaminated materials. Always perform the decontamination procedure prior to returning the SpotOn temperature monitoring system for service and prior to disposal. 8. To reduce the risks associated with entanglement: Do not leave pediatric patients unattended while using the SpotOn temperature monitoring system.
8 6 Introduction CAUTIONS 1. To reduce the risks associated with skin maceration: Do not use the sensor on damaged or compromised skin. 2. To reduce the risks associated with cross-contamination: Clean the sensor cable before connecting to a new sensor. 3. To reduce the risks associated with impact and facility medical device damage: Do not use the SpotOn control unit as a handle to transport or to move the device to which it is attached. Do not initiate temperature monitoring unless the SpotOn control unit is safely placed on a hard, flat surface or is securely mounted. 4. To reduce the risks associated with environmental contamination: Follow applicable regulations when disposing of this device or any of its electronic components. NOTICES 1. The SpotOn temperature monitoring system meets medical electronic interference requirements. If radio frequency interference with other equipment should occur, connect the unit to a different power source. 2. Federal law (USA) restricts this device to sale by or on the order of a licensed healthcare professional. 3. To avoid SpotOn temperature monitoring system damage that may impact performance: Do not store the SpotOn control unit and system components in a wet or damp place. Do not spray cleaning solutions onto the control unit or into the sensor cable connector. Do not immerse the SpotOn temperature monitoring control unit or system components in any liquid or subject them to any sterilization process. Do not use solvents such as acetone or thinner to clean the control unit; avoid abrasive cleaners. Clean control unit exterior with a damp soft cloth and 70% mixture of isopropyl alcohol and water. For full cleaning procedures see Section 5: General Maintenance on page 21. Do not immerse any of the devices or use a dripping wet cloth for cleaning. 4. The SpotOn temperature monitoring sensor is not made with natural latex material. 5. To the full extent permitted by law, the manufacturer and/or importer declines all responsibility for injury resulting from the unit being used in conjunction with unapproved system components. Proper use and maintenance Arizant Healthcare Inc., a 3M company assumes no responsibility for the reliability, performance, or safety of the temperature monitoring system if the following events occur: Modifications or repairs are performed by unqualified personnel. The unit is used in a manner other than that described in the Operator s Manual. The unit is installed in an environment that does not meet the appropriate electrical requirements. Read before servicing equipment All repair, calibration, and servicing of this equipment must be performed by 3M Patient Warming. There are no user serviceable parts inside the equipment or power supply.
9 Introduction 7 Description of the SpotOn temperature monitoring system The SpotOn temperature monitoring system measures the core temperature of the patient. The system is comprised of the SpotOn temperature sensor, which connects to the SpotOn control unit through the sensor cable, a power supply, and an optional monitor cable. For additional sensors, sensor cable, power supply, control unit stand, monitor cable, hook-and-loop, or foam adhesive, contact 3M Patient Warming. Monitor Cable Power Supply 3M SpotOn Control Unit Sensor Cable PATIENT SENSOR Temperature Sensor Sensor Connector Figure 1-1: SpotOn Temperature Monitoring System A
10 8 Introduction How it works The SpotOn temperature monitoring system uses zero-heat-flux thermometry to accurately measure a person s core temperature as characterized in Figure 1-2 below. 1) The SpotOn temperature monitoring system gently warms the sensor creating an isothermal pathway under the sensor. 2) Once equilibrated to the core temperature, skin-surface heat loss to the environment is prevented and a zero-heat-flux condition is established. 3) When the temperature sensor reaches equilibrium with the patient s core temperature, the SpotOn control unit displays an accurate, noninvasive measurement of the patient s core temperature. Skin Surface Temperature Sensor Deep Tissue 1) Placement and connection 2) Equilibration - isothermal pathway development 3) Equilibrated - isothermal pathway established Figure 1-2: Isothermal pathway formation with zero-heat-flux technology SpotOn control unit The SpotOn control unit displays non-invasive core temperature measurements obtained from the SpotOn temperature sensor. The current temperature is displayed numerically, and previous temperature data is displayed graphically as a temperature trend graph. When the sensor is plugged into the sensor cable and equilibration is complete, the control unit reads up to the last two hours of stored temperature data and displays the temperature trend graph. Disconnections of the sensor from the sensor cable are indicated by gaps in the temperature trend graph. The current temperature measurement can be continuously transmitted to a patient vital signs monitor through the optional SpotOn monitor cable using a standard YSI-400 type input. SpotOn temperature sensor The SpotOn sensor is constructed of two layers of medical grade foam and a flexible circuit which contains a resistive warming circuit, two calibrated thermistors, and nonvolatile memory. The information that generates the temperature trend graph is stored on the SpotOn sensor. When the patient is transferred from one location to another, the SpotOn sensor is disconnected from the SpotOn sensor cable so the sensor is left in place on the patient. The SpotOn sensor may be reconnected to a different SpotOn sensor cable and control unit when the patient arrives at the next point of care. Once the SpotOn sensor is reconnected to the SpotOn sensor cable, the system will begin to reequilibrate and will regenerate the stored temperature trend graph and display the patient s current temperature. The act of disconnecting and reconnecting the SpotOn sensor from the sensor cable is indicated by a gap in the temperature trend graph.
11 Installation 9 Section 2: Installation WARNING: 1. To reduce the risks associated with access to critical patient information or equipment do not mount the control unit: To a surface that is not flat or clean. Over air vents of other equipment. Over controls, displays, or buttons of other equipment. Over speakers or alarms of other equipment. Mounting the SpotOn control unit CAUTION: To prevent injury, mount the SpotOn temperature monitoring system at a height no higher than 84 (213 cm). 1. Use the provided hook-and-loop or foam adhesive to secure the control unit stand to any hard, flat surface (use only the 3M provided/specified control unit mounting materials). Note: Confirm the hook-and-loop is securely fastened together before mounting the control unit to a surface. Recommend: Clean surface with a 70% mixture of isopropyl alcohol and water prior to applying the provided hook-and-loop or foam adhesive. 2. The SpotOn control unit s height and orientation can be adjusted by loosening/tightening the control unit stand knob on the back of the unit. Figure 2-1: Control Unit Mounting Configuration A
13 Display Panel 11 Section 3: Display Panel Display screens Start-up The start-up screen displays for approximately five seconds when the control unit is initially powered ON. The revision number of the control unit software is also displayed. FW-x.x.xxx Standby The SpotOn system graphic is displayed when the unit is not in use. 3M SpotOn Temperature Monitoring System A
14 12 Display Panel Ready The ready screen displays the serial number of the SpotOn sensor and indicates the SpotOn sensor cable and sensor are properly attached to the SpotOn control unit. The SpotOn sensor is now ready to be attached to the patient. SN Equilibration A flashing yellow temperature display indicates the sensor has been connected to the patient and to the control unit and is in the process of equilibration. The graph below the temperature output indicates the progress of equilibration. This process will take approximately three minutes. If you see a temperature in the upper left hand corner of the screen, that is the last recorded temperature that has been captured by the sensor. The sensor captures and records a temperature every five minutes. After the equilibration is complete, the core temperature of the patient is displayed on the SpotOn control unit in bold white numbers and can be automatically transmitted to the patient monitor via the monitor cable C C Running The running screen displays the core temperature of the patient in white. The trend graph at the bottom of the screen displays up to the last two hours of the patient s temperature in five minute increments. The bars on the graph will begin filling from the right with the 36 C always visible. The blue bars indicate that the temperature dropped below 36 C (white indicates the temperature is above 36 C). Control unit error The SpotOn control unit error screen displays when there is a system error. Discontinue use of unit. Contact a biomedical technician. Sensor error The sensor error screen displays when there is a temperature sensor or cable error. See Section 4: Troubleshooting on page 13 for details. E-xx E-xx
15 Troubleshooting 13 Section 4: Troubleshooting The following conditions are listed in the order of which troubleshooting actions should be performed. On Mode Condition Cause Action Unit does not power up. Displays Unit is not plugged in, or power supply is not plugged into an appropriate outlet. Unit failure. Condition Cause Action Ready screen continues to display while sensor is adhered to the patient. SN Running screen does not appear on the control unit. Sensor not properly adhered to the patient. Low patient temperature (below 29 C). Control unit failure. Control unit may still be equilibrating. Control unit failure. Make sure the power supply is plugged into the control unit. Make sure the control unit is plugged into an appropriate power outlet. Contact 3M Patient Warming technical service. Make sure the sensor is connected to the patient. Press and hold the C/ F button on the back of the control unit for five seconds to force the control unit into equilibration mode. The patient s temperature will then display. Discontinue use of unit. Contact 3M Patient Warming technical service. Wait until the SpotOn control unit has finished equilibration. Continue use. Contact 3M Patient Warming technical service. Patient temperature does not appear on the patient monitor C The patient s temperature output on the control unit and patient monitor does not read the same value. C Control unit may still be equilibrating. Monitor cable is not plugged in. Cable failure. Control unit failure. Cable failure. Wait until the SpotOn control unit has finished equilibration. Continue use. Make sure the monitor cable is plugged into the control unit and patient monitor. Replace monitor cable. Contact 3M Patient Warming technical service. Contact 3M Patient Warming technical service after use. Confirm SpotOn monitor cable is being used. Replace monitor cable. Check resistance of cable. Contact 3M Patient Warming technical service A
16 14 Troubleshooting Errors Error Screen Condition Cause Action E-xx E-xx E-1 through E-99 Sensor not properly connected to the sensor cable. Sensor failure. Cable failure. Make sure the sensor is connected to the sensor cable, by disconnecting and reconnecting the sensor. Replace sensor. Replace sensor cable. Contact 3M Patient Warming technical service. E-100 and up Control unit failure. Disconnect the unit from power source. Allow seconds for the unit to reset. Reconnect the unit to the power source to determine if the unit reset or if it is a permanent error. Discontinue use of the unit. Contact a biomedical technician.
17 Calibration Verification Stick 15 Section 5: Calibration Verification Stick Calibration verification frequency Every 12 months or according to institutional protocol. Tools and equipment Calibrated digital multi-meter Model Calibration verification stick Method 1. Connect the power supply to the back of the SpotOn control unit (see Figure 5-1: Back of Control Unit). Plug the power supply into an appropriate outlet. The standby screen will illuminate. 2. Connect the SpotOn sensor cable to the front of the control unit (see Figure 5-2: Front of Control Unit). Stand Knob Digital Port (used by 3M personnel only) C/ F Temperature Display Button Monitor Cable Port Power Input Port Figure 5-1: Back of Control Unit Figure 5-2: Front of Control Unit A
18 16 Calibration Verification Stick 3. Connect the SpotOn calibration verification stick to the sensor cable. Ensure the verification stick is fully inserted into the sensor cable. 4. The screen shows the actual calibrated thermistor readings for the skin and heater thermistors. The calibration verification stick contains a precision resistor for each calibrated thermistor with a known reference value corresponding to a reference temperature. Verify that the reference temperature for each calibrated thermistor matches the displayed value (36.0 ± 0.1 C, 96.8± 0.2 F) 5. If the reference temperatures are within acceptable limits, continue with steps below. If the reference temperatures are outside of the acceptable limits, discontinue use of the SpotOn temperature monitoring system. Contact 3M patient warming technical service at Figure 5-3: Calibration screens (Celsius and Fahrenheit) 6. Plug the monitor cable to the monitor port on the back of the control unit. 7. Wait for the control unit to calibrate and start emulating data. The internal relay will click and the display will refresh when the emulation is active. 8. Set the multi-meter to the 2000 ohm range. Note: Zero the multi-meter as necessary for all resistance measurements. 9. Hold the digital multi-meter leads to the tip and the ring on the end of the monitor cable. 10. Confirm the reading on the multi-meter is 1412 ohms + / 15 ohms. 11. If the reading on the multi-meter is within acceptable limits, return the SpotOn temperature monitoring system to use. If the reference reading on the multi-meter is outside of the acceptable limits, discontinue use of the SpotOn temperature monitoring system. Contact 3M patient warming technical service at
19 General Maintenance 17 Section 6: General Maintenance Cleaning and disinfecting procedure CAUTION: Do not immerse any of the devices or use a dripping wet cloth for cleaning. Moisture may seep inside the device and damage the electrical components and lead to incorrect temperature reporting. Do not spray cleaning solutions onto the control unit or into the sensor cable connector. Damage to the control unit or sensor cable connector may occur. Cleaning the control unit and sensor cable Clean the SpotOn control unit on an as-needed basis or per facility policies and procedures for cleaning electronic equipment. Clean the sensor cable between each use. 1. Disconnect power supply from power outlet. 2. Use a slightly damp soft cloth moistened with a mild, nonabrasive cleaning solution to clean the device surfaces, cords, and cables. Avoid getting liquid into electronic ports. 3. Dry with a separate soft cloth. Disinfecting the sensor cable 1. Clean the devices as described above. 2. Wipe down the control unit and cable using a damp soft cloth and 70% isopropyl alcohol solution. Avoid getting liquid into electronic ports. 3. Dry with a separate soft cloth. Storage Notice: Do not store the SpotOn control unit and system components in a wet or damp place. Damage to the electrical components may occur. Store all SpotOn components at room temperature and in a dry place when not in use. Service All service must be performed by 3M Patient Warming or an authorized service technician. Call 3M Patient Warming Customer Service at for service information A
21 Specifications 19 Section 7: Specifications Physical characteristics Dimensions of Control Unit 9.3 cm (3.7 in) high, extendable to 11.4 cm (4.5 in) high 7.1 cm (2.8 in) wide, 4.3 cm (1.7 in) deep Weight of Control Unit 128 g (4.5 oz) Dimensions of Sensor 4.1 cm (1.6 in) diameter, 0.5 cm (0.2 in) thick Length of the Sensor Cable 400 cm (158 in) Classification MEDICAL - GENERAL MEDICAL EQUIPMENT AS TO ELECTRICAL SHOCK, FIRE AND MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH UL ; CAN/ CSA-C22.2, No ; ANSI/AAMI ES :2005 CSA-C22.2 No :08; Control No. 4HZ8. No.4HZ8 Classified under IEC Guidelines (and other national versions of the Guidelines) as Class II, Type CF, Defibrillation-Proof, Ordinary Equipment. Conforms to EN Not suitable for use in the presence of flammable anesthetic mixtures with air or nitrous oxide. Classified by Underwriters Laboratories Inc. with respect to electric shock, fire, and mechanical hazards only, in accordance with UL , IEC , and Canadian/CSA C22.2 No ANSI/AAMI ES ; 2005.Classified under the Medical Device Directive as a Class IIb device. Accuracy 25 C to 43 C ± 0.2 C Sensor Material Medical grade foam and adhesive PET flexible circuit Recommended Calibration Check Every 12 months or according to institutional protocol. Sensor Shelf Life 36 months Digital Port (used by 3M personnel only) Serial output 0 [-12 to + 12] Monitor Cable Port Provides a resistance that corresponds to a YSI-400 thermistor at the displayed temperature. It is electrically isolated from the SpotOn control unit A
22 20 Specifications Electrical characteristics External power supply VAC, Hz Output; 5 VDC Class II, double insulated medical grade Maximum heating power 2 W Temperature characteristics Over-temperature cutoff 43 C - Skin thermistor reading 44.5 C - Heater thermistor reading Performance characteristics Equilibration time Approximately three minutes Time response Approximately three minutes Measurement locations Patient s lateral forehead above the orbital ridge Measurement range 25 C - 43 C Measurement readout Celsius or Fahrenheit Leakage current CF classification. Meets leakage current requirements in accordance with UL and IEC Environmental conditions Ambient temperature range 10 C to 40 C (50 F to 104 F) Storage and transport temperature range -20 C to 60 C (-4 F to 140 F) Store all components at room temperature and in a dry place when not in use. Operating humidity 10 to 75% RH, noncondensing Atmospheric pressure range 80 kpa to 106 kpa (12 PSI to 15 PSI) Oxygen environment The sensor only is suitable for use in the presence of an oxygen enriched environment.
24 Made in the USA by 3M Health Care. 3M is a trademark of 3M Company, used under license in Canada. SPOTON is a trademark of Arizant Healthcare Inc., used under license in Canada Arizant Healthcare Inc. All rights reserved. 3M Deutschland GmbH, Health Care Business Carl-Schurz-Str. 1, Neuss, Germany 3M Health Care, 2510 Conway Ave., St. Paul, MN USA TEL A 05/13
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Flopurge TS Operation Manual Part Number 079-0204 Spectron Gas Control Systems United Kingdom Unit 4, Herald Court, University of Warwick Science Park, Coventry, CV4 7EZ +44 (0)24 7641 6234 firstname.lastname@example.org
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General Information Use The Air drill System is a pneumatic powered system used for many applications orthopedic and trauma surgery. To ensure proper operation of the air drill, use only original attachment
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Infrared Portable Space Heater 1500 Watts with Two Heat Settings Automatic Thermostat Tip-Over Switch Overheat Thermal Cut-Off Protection Room Temperature LED Display Precision Temperature Control Easy
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USER MANUAL PORTABLE OXYGEN CONCENTRATOR Model: PM4150 Series SAVE THESE INSTRUCTIONS Federal (USA) law restricts this device to sale by or on the order of a physician. 300 Held Drive Tel: (+001) 610-262-6090
DIGITAL INDICATOR JIR-301-M Instruction Manual Preface Thank you for purchasing our digital indicator JIR-301-M. This manual contains instructions for the mounting, functions, operations and notes when