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
Operator s Guide Autoclavable Internal Handles with Integrated Paddles 9650-0550 Rev. M The issue date for the Autoclavable Internal Handles with Integrated Paddles Operator s Guide (REF 9650-0550 Rev.
Digital Heat Block User Manual Quidel Digital Heat Block Page 1 of 10 General Information Quidel Contact Information Contact Quidel Technical Support from 8:00 a.m. to 5:00 p.m. EST Tel: 800.874.1517 (in
OM-E0799E 000 English Thank you for purchasing VIVA ace Motor Kit. Please read this Operation Manual and the VIVA ace Basic Set Operation Manual carefully before use for operating instructions and care
Cascade Comfort Bathing Systems with Aqua-Aire Safe Operation & Daily Maintenance Instructions PENNER PATIENT CARE, INC Box 523 / 101 Grant St. Aurora, NE 68818 560750 Revision A 12/11/15 1-866-PENNERS
Non-Touch Thermometer User Manual ARC Devices Ltd. Copyright ARC Devices Ltd. 2016 Welcome to your new state of the art ARC InstaTemp digital infrared non-touch thermometer! The ARC InstaTemp is a digital
User Manual Non-contact Infrared Thermometer www.paryvara.com firstname.lastname@example.org Introduction Thank you for purchasing this Non-contact Infrared Thermometer. Please read the User Manual carefully to ensure
Bair Paws Model 850 Warming Unit Service Manual Warning: Electrical Shock Hazard. There are electrically live parts within the warming unit when it is connected to a power source, even when the hand-held
Rad-5 & Rad-5v Signal Extraction Pulse Oximeter Service Manual (Place Logo from Lab- 1874 here) Rad-5 & Rad-5v Signal Extraction Pulse Oximeter Service Manual The Rad-5/5v Service Manual is intended to
PAGE OF NON-TOUCH THERMOMETER User Manual ARC Devices USA Inc. Copyright 201 4-2017 ARC Devices USA Inc. For use in Canada PAGE 2 OF 24 INTRODUCTION Welcome to your new state of the art ARC InstaTemp digital
User's Guide CO 2 Monitor Model CO200 Introduction Congratulations on your purchase of this Model CO200 Carbon Dioxide Meter. This meter measures CO2 level, air temp., humidity, date and time. With visible
INSTRUCTIONS Reacti-Therm I and III Heating Modules TS-18822 TS-18824 Number TS-18822 TS-18824 Description Reacti-Therm I Heating Module (single block) Reacti-Therm III Heating Module (triple block) 2101.1
Safe Operation Manual Honeywell IQ Force Gas Detector Honeywell Analytics 800-663-4164 403-248-9226 Fax 403-575-3708 03JUN2012 P/N 50105843-047 Version 01 http://www.honeywell.com HONEYWELL IQ Force PERSONAL
U S E R M A N U A L Models: PM15F (shown) PM15P SAVE THESE INSTRUCTIONS CAUTION Federal (USA) law restricts this device to sale by or on the order of a physician. 300 Held Drive Tel: 610-262-6090 Northampton,
Your healthy living center www.obbomed.com User s Manual Version 1.0, 2014.12 Alternating Air Mattress CONTENTS Important Safeguards Statements &Symbols Introduction Product Functions Installation Operation
Torrent irrigation pump Reorder No. 00711569 Operating and Maintenance Manual 00732292 Rev. D Issued Date: August 2018 Warning: An issued or revision date for these instructions is included for the user
GigaCore 12 Gigabit Ethernet Switch for the entertainment industry Quick Start Guide V2.1.0 Rev5 English Table of Content Safety Instructions 3 Compliance information 4 Warranty information 5 Registration
AIR EXPRESS LAL P1500 LOW AIR LOSS THERAPY SYSTEM REF C1500 Control Unit REF M1500 Mattress Operator s Manual P/N 11882-000 6/03 Air Express LAL Before you begin Table Of Contents Section Description Page
WARM LINE IV Fluid Warmer Product Code: J1448 JORGENSEN LABORATORIES PHONE 800-525-5614 FAX 970-663-5042 email@example.com Warm Line IV Fluid Warmer Portable and light weight Only warms IV fluids not transfusion
Network Camera Quick Guide DC-T1233WHX Powered by Safety Precautions WARNING RISK OF ELECTRIC SHOCK DO NOT OPEN WARNING: TO REDUCE THE RISK OF ELECTRIC SHOCK, DO NOT REMOVE COVER (OR BACK). NO USER-SERVICEABLE
Installation Instructions 3M Light Mat Series 3635-1000 Installation Bulletin 3635-1000 Release D, Effective July 2010 (Replaces C, Apr 2010) See Bulletin Change Summary at end of Bulletin Product Description
User Manual for Breas HA 01 Humidifier 1 Intended Use of the Breas HA 01 Humidifier Read this manual thoroughly so that you completely understand how the humidifier is operated and maintained before taking
Instruction Manual Model AccuPlate Hotplate AccuPlate Stirrers AccuPlate Hotplate Stirrer 12/10 CLS-EQ-LHP01REV2 9296050000 About This Manual This manual is designed to assist you in optimal usage of your
User s Manual Warm N Cozy Point A Technologies, Inc. 20957 Currier Road, Unit C, Walnut, CA 91789 U.S.A. TABLE OF CONTENTS Page 1. Safety Procedures and Precautions...3 2. Electrical Information......4
Operator s Manual The Quietek Congratulations! Congratulations on your purchase of the Quietek euthanization system. Please read this operator s manual which explains proper operation of the instrument.
ANGELUS (Ver 2.03) Patient Monitoring System CONTENT Contents of Manual 1 Meaning of Symbols used in this manual 2 Section 1. GENERAL 3 1.1 Introduction 4 1.2 Composition of unit 8 1.3 Panel Description
Veterinary Patient Warming System Service Manual For information on operating the Hot Dog Patient Warming System, refer to the Instructions for Use Hot Dog TM Patient Warming System Service Manual Page
Health Check Ear and Forehead Thermometer Model No.: 70125 Instruction Manual Thank you for choosing our Health Check Thermometer. This high-tech instrument measures body temperature via reflected infrared
ENGLISH Kinsa Smart Ear ThermometerTM Instructions For Use Thank you for purchasing the Kinsa Smart Ear Thermometer, a professionally accurate instrument for fast and easy temperature taking in the ear.
Adtemp TM 427 TempleTouch TM Thermometer USE, CARE & MAINTENANCE Intended Use: A Temple Touch thermometer is a device which enables accurate body temperature measurements obtained by using a unique probe,
HIn3550 Magnetic Field Monitor User's Manual Copyright 1993 by Holaday Industries, Inc. Manual #600053 10/97 $12.50 Revision Record Manual #600053 HIn3550 Magnetic Field Monitor Revision Description Date
Limited Warranty Global Medical Holdings (GMH) warrants the MaxiCompressor for 1 year from the date of purchase due to faulty parts or workmanship. This warranty is limited to the original purchaser of
ATOMLAB XENON TRAP MONITOR OPERATION AND INSTALLATION MANUAL 136-755 FN: 12-148 5/12 This manual contains installation and operation procedures for the following product: 136-755 Atomlab Xenon Trap Monitor
RADS-51J RADS-61J Owner s Manual Room Air Conditioner with R-410A Heat Controller, Inc. 15 16 Contact an authorized service technician for repair or maintenance of this unit. Contact an authorized installer
TIH 300 S / TIH 400 S / TIH 500 S / TIH 700 S / TIH 900 S / TIH 1100 S EN OPERATING MANUAL INFRARED HEATING PANEL TRT-BA-TIH300S-TIH400S-TIH500S-TIH700S-TIH900S-TIH1100S-TC-002-EN Table of contents Notes
1500W CERAMIC HEATER GVACH110 Instruction Manual Contents Guide to the Appliance 2 Caring for the Environment 3 Safety Information and Warnings 4 Operation Instructions 5 Care and Maintenance 6 Technical
Product Manual Manuel D utilisation Bedienungshandbuch Manual Del Producto Manuale Prodotto Producthandleiding *smith&nephew VERSAJET HYDROSURGERY SYSTEM VERSAJET Hydrosurgery System Product Manual Contents
Alice In Wall Recessed Electric Fireplace Model Number: (EF172B, EF173B, EF174B, EF175B, EF176B) OWNER S MANUAL WARNING Read and understand this entire owner s manual, including all safety information,
APC BC300 Series 40kW 208/450/480V User Guide Copyright 2002 APC Denmark ApS This manual is subject to change without notice and does not represent a commitment on the part of the vendor Thank You Thank
System One Heated Humidifier USER MANUAL 2016 Koninklijke Philips N.V. All rights reserved. Table of Contents Intended Use... 2 Warnings... 2 Cautions... 2 Contraindications... 3 Symbol Key... 3 System
10,000 BTU Portable Air Conditioner User Guide IVAPAC10KBTU Thank you for purchasing the Ivation 10,000 BTU Portable Air Conditioner. This User Guide is intended to provide you with guidelines to ensure
Quick Touch Pendant User Guide 2018 RF Technologies, Inc. All specifications subject to change without notice. All Rights Reserved. No Part of this work may be reproduced or copied in any form or by any
CLETEF-786 0482 Infrared Thermometer Instruction Manual Introduction Thank you for choosing the Clever Choice Duo TM Ear & Forehead Thermometer, by Simple Diagnostics. The infrared thermometer CLETEF-786
AS 500 Instructions for Use 1 Contents General Notes... 3 Safety standard... 3 Safety Precautions... 4 Device out of use:... 4 Description of the Device / Proper Usage... 5 Technical data...5 Laser probe...
Forehead Infrared Thermometer Model 09-347 3-YEAR INSTRUCTION MANUAL ENGLISH & ESPAÑOL Please read this instruction manual completely before operating this unit. STOP! PLEASE ENSURE YOU HAVE ALL OF THE
Moduflex Dry Air System Desiccant Air P3TJA13A1AN - P3TJA13A7AN EN USER GUIDE (Original Language) NL DE FR FI SV NO DA EL ES PT IT PL SK CS ET HU LV LT RU SL TR MT CONTENTS 1 Safety Information...2 1.1
Classic Twelve O clock Cabinet Installation Instructions CF36 CF42 THIS MANUAL IS FOR AUTHORIZED AND QUALIFIED INSTALLATION PERSONEL ONLY! Table of Contents General Information... 3 CF36 Cabinet Overview...
12L DEHUMIDIFIER OPERATING INSTRUCTIONS Attention: This Dehumidifier is rated to extract 12L per day in an environment of 80% humidity and temperature of 30 C. This is the world-wide standard for rating
OPERATING INSTRUCTIONS AND MAINTENANCE MANUAL S-SCORT II Model 15006 SSCOR, INC. 11064 Randall Street Sun Valley, CA 91352 USA Telephone +1-818-504-4054 800-434-5211 Fax +1-818-504-6032 www.sscor.com Email:
CareTemp Touch Free Thermometer Directions for use 2017 Welch Allyn. All rights are reserved. To support the intended use of the product described in this publication, the purchaser of the product is permitted
Instruction Manual for Soldering / SMD Rework Station LF-16 1680 For Lead-free soldering application and rework on professional SMD electronics. INTRODUCTION Thank you for purchasing Xytronic s soldering
Installation, Operation & Maintenance Manual Portable Room Air Conditioner and Heat Pump PS-121B PSH-141A Thank you for purchasing our Portable Air Conditioner. French version of this manual is available
Superior Spa with Aqua-Aire Safe Operation & Daily Maintenance Instructions PENNER PATIENT CARE, INC Box 523 / 102 Grant St. Aurora, NE 68818 350750 Rev H 08/28/2014 1-866-PENNERS 1-866-736-6377 1-800-732-0717
Instructions For Use Hybernite ROC 2300 Rainout Control System The Hybernite Rainout Control System helps to prevent moisture condensation in the breathing tube of adult patients requiring continuous positive
TEMPERATURE MANAGEMENT SYSTEM SERVICE MANUAL Simply Advanced TM TEMPERATURE MANAGEMENT SYSTEM AS5000 SERVICE MANUAL TABLE OF CONTENTS Chapter 1 Getting Started...1 Introduction...1 Indications for Use...1
HOBO U14 Data Logger User Manual The U family of data loggers offers reliability and convenient monitoring for applications that require higher accuracy, better resolution, more memory, or USB connectivity
5580 S. Nogales Highway Tucson, AZ 85706 Phone: (800) 975-7987 Fax: (520) 294-6061 www.westmedinc.com TM ANAPOD Instructions For Use PN 75054, Rev 02 ii TABLE OF CONTENTS Servicing: Beyond the replacement
2200W RADIANT HEATER GVARH350 Instruction Manual Contents Guide to the Appliance 2 Caring for the Environment 3 Safety Information and Warnings 4 Operation Instructions 5 Care and Maintenance 6 Technical
Utopian Split A/C Thank you for purchasing this quality Split A/C system! Please read through this manual completely, and keep it in case you need to reference the information in the future. Any operation
INSTALLATION MANUAL GUTHD2 Universal Two Way Digital Thermostatic Valve for Shower Systems IMPORTANT: To ensure this product is installed properly, you must read and follow these guidelines. The owner/
MODEL 7000 SUCTION UNIT OPERATOR S MANUAL Caution Federal law restricts this device to sale by or on order of a physician, or any other practitioner licensed by the law of the State in which he practices
Instructions ON/OFF Consumer Info-Line 1-800-363-2381 Model / Modèle : 016-670 Made and printed in Taiwan for: A.M.G. Medical Inc. 8505 Dalton, Montréal, QC H4T 1V5 Canada 1-800-363-2381 AMG Medical, Inc.
Model G32-S Model G32-E Disinfection Soak Stations Operator s Manual CIVCO Medical Solutions 102 First Street South Kalona, IA 52247 USA Tel: 1-800-445-6741 Fax: 1-877-329-2482 Website: WWW.CIVCO.COM Copyright
REFRIGERATOR USE DF1-15 Fridge BEFORE USING THE APPLIANCE. Your new appliance is designed exclusively for domestic use. To ensure best use of your appliance, carefully read the operating instructions which
OMNI Express VS VERSATILITY IN VITAL SIGNS OMNI Express VS TOUCHSCREEN easy and intuitive to use PORTABLE weighs less than 6lbs MOBILE backup battery powered The Omni Express VS is a new intuitive approach
U S E R M A N U A L Model: PM5900 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 Northampton, PA 18067
Instruction Manual For All Corning Hot Plates, Stirrers, Stirrer/Hot Plates with Digital Displays, and External Temperature Controller (6795PR) Corning Cat. No. 230V 230V Model No. Product Top Plate Size
The Impact the Reference Standards in the 2012 Edition of NFPA 101 have on the Operation of Health Care Facilities: NFPA 80 and 99 Sharon S. Gilyeat, P.E. Lauren Schrumpf August 8, 2018 Expertly Engineering
Tissue Flotation Bath Flotation Work Station Catalog # TFB-S-120, TFB-L-120 TFB-S-220, TFB-L-220 FWS-S-120, FWS-L-120 FWS-S-220, FWS-L-220 Operator s Manual Version 1.3, Jan 2012 Be certain to read this
CLASSIC SIDE CABINET Installation Instructions THIS MANUAL IS FOR AUTHORIZED AND QUALIFIED INSTALLATION PERSONAL ONLY! Table of Contents General Information...3 CCS Overview...4 CCS Cabinet Dimensions...5