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SpotOn
TM
Temperature Monitoring System website to ensure you have the most recent version of this document. www.spotontemperature.com reorder #202052A
6 Introduction
English 202052A
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, at 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. e SpotOn temperature monitoring system meets medical electronic interference
requirements. If radio frequency interference with other equipment should occur, connect the
unit to a dierent 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 so cloth and 70% mixture of isopropyl alcohol
and water. For full cleaning procedures see “Section 5: General Maintenance, Storage and
Service” on page 17.
• Do not immerse any of the devices or use a dripping wet cloth for cleaning.
4. e 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:
• Modications or repairs are performed by unqualied personnel.
• e unit is used in a manner other than that described in the Operator’s Manual.
• e 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.
• ere are no user serviceable parts inside the equipment or power supply.