3M 370 Marine Instruments User Manual


 
Introduction 5
English 202052A
Check the 3M
TM
SpotOn
TM
Temperature Monitoring System website to ensure you have the most recent version of this document. www.spotontemperature.com reorder #202052ACheck the 3M
TM
SpotOn
TM
Temperature Monitoring System website to ensure you have the most recent version of this document. www.spotontemperature.com reorder #202052A
WARNINGS
1. To reduce the risks associated with access to critical patient information or equipment:
• e 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, re, 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 re:
• Keep power supply visible and accessible at all times. e plug on the power supply serves
as the disconnect device. e power outlet shall be as close as practical and shall be easily
accessible.
• Use only the power supply specied for this product and certied 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 1-800-733-7775 or 952-947-
1200.
• Do not service or modify the power supply, control unit, cables, sensor, or any part of the
3M SpotOn system. ere are no user serviceable parts.
4. To reduce the risks associated with re:
• is system is not suitable for use in the presence of a ammable 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 uids.
• Use an additional independent thermometer to measure body temperature during
intentional hyperthermia or hypothermia therapy.
• Conrm 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 aect 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.