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3
SpotOn™ Temperature Monitoring System
Model 370
Operator’s Manual
1 3M™ SpotOn™ Temperature Monitoring System
•Model370•Operator’sManual
2 Système de surveillance de la température 3M™ SpotOn
•Modèle370•Manueld’utilisation
3 3M™ SpotOn™ Temperaturüberwachungssystem
•Modell370•Bedienerhandbuch
4 3M™ SpotOn™ Sistema di monitoraggio della temperatura
•Modello370•Manualedell’operatore
5 3M™ SpotOn™ Sistema de control de temperatura
•Modelo370•Manualdeloperador
6 3M™ SpotOn™-temperatuurcontrolesysteem
•Model370•Gebruikershandleiding
7 3M™ SpotOn™Temperaturövervakningssystem
•Modell370•Bruksanvisning
8 3M™ SpotOn™ temperaturovervågningssystem
•Model370•Brugervejledning
9 3M™ SpotOn™temperaturovervåkingssystem
•modell370•Brukerhåndbok
0 3M™ SpotOn™-lämpötilanseurantajärjestelmä
•Malli370•Käyttöopas
- Sistema de Monitorização da Temperatura 3M™ SpotOn™
•Modelo370•Manualdoutilizador
™
™
3M™ SpotOn
Temperature Monitoring System
TM
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Revision History
Revision Reason for Change Pages Affected Date
370096
A
370096
B
370096
C
202052
A
New Revision - First Release All May 2012
Languages Added 25-155 May 2012
Added specifications and added
languages
Update company address All
All
February
2013
May
2013
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Operator’s Manual
Model 370
™
3M™ SpotOn
Temperature Monitoring System
English 5
Français 23
Deutsch 47
Italiano 71
Español 95
Nederland 119
Svenska 143
English 202052A
Dansk 167
Norsk 191
Suomenkielinen 215
Português 239
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English
1 3M™ SpotOn™ Temperature Monitoring System
•Model370•Operator’sManual
™
3M™ SpotOn
Temperature Monitoring System
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1
Table of Contents
Section 1: Introduction �������������������������������� 3
About this manual ��������������������������������� 3
Intended use ������������������������������������ 3
Safety information and symbols ������������������������� 3
Proper use and maintenance ��������������������������� 6
Read before servicing equipment ������������������������� 6
Section 2: Overview and Operation ������������������������ 7
Description of the SpotOn temperature
monitoring system ��������������������������������� 7
How does it work? ������������������������������� 8
SpotOn control unit ���������������������������� 8
SpotOn temperature sensor ������������������������ 8
Back of Control Unit �������������������������������� 9
Front of Control Unit �������������������������������� 9
Setting up the SpotOn control unit ������������������������ 9
Instructions for use �������������������������������� 10
Transferring the patient and sensor �������������������� 11
Removing the sensor ����������������������������� 11
To change temperature unit display
(Celsius or Fahrenheit) ������������������������������ 12
Shutting down the control unit ������������������������� 12
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Section 3: Display Panel ������������������������������ 13
Display screens ���������������������������������� 13
Start-up ������������������������������������ 13
Standby ������������������������������������ 13
Ready ������������������������������������� 14
Equilibration ��������������������������������� 14
Running ������������������������������������ 14
Control unit error ������������������������������� 14
Sensor error ���������������������������������� 14
Section 4: Troubleshooting ���������������������������� 15
On Mode �������������������������������������� 15
Displays �������������������������������������� 15
Errors ��������������������������������������� 16
Section 5: General Maintenance, Storage and Service ������������ 17
Cleaning and Disinfecting Procedure ���������������������� 17
Cleaning the control unit and cable ��������������������� 17
Disinfecting the sensor cable ������������������������ 17
Storage �������������������������������������� 17
Service ��������������������������������������� 17
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2 Introduction
Section 6: Technical Service and Order Placement ��������������������� 19
When you call for technical support ����������������������������� 19
Technical service and order placement ��������������������������� 19
USA ��������������������������������������������� 19
Outside of the USA ������������������������������������� 19
Section 7: Specifications ������������������������������������ 21
Physical characteristics ������������������������������������ 21
Electrical characteristics ������������������������������������ 22
Temperature characteristics ���������������������������������� 22
Performance characteristics ��������������������������������� 22
Leakage current �������������������������������������� 22
Environmental conditions ����������������������������������� 22
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Introduction 3
Section 1: Introduction
About this manual ............................................................................... 3
Intended use .................................................................................... 3
Safety information and symbols ................................................................... 3
Explanation of signal word consequences .......................................................... 4
Proper use and maintenance ...................................................................... 6
Read before servicing equipment .................................................................. 6
About this manual
is Operator’s Manual describes the setup, use, and maintenance of the 3M™ SpotOn™ temperature
monitoring system. e SpotOn temperature monitoring system and the manual are to be used by
healthcare professionals in clinical environments only. Read and follow all instructions, labeling and
accompanying documents supplied with this SpotOn temperature monitoring 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
CAU TION
is system is subject to the European WEEE Directive 2002/96/EC.
Debrillation-proof type CF applied part
English 202052A
is 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.
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4 Introduction
Class II equipment
Authorized Representative in the European Community
CAUTION: Recycle to avoid environmental contamination
Direct current
See accompanying documents
is product contains recyclable parts. For information on recycling - please
contact your nearest 3M Service Center for advice.
Follow instructions for use
Keep dry
Hardware temperature limits
Sensor temperature limits
Explanation of signal word consequences
damage only.
English 202052A
WARNING:
in death or serious injury.
CAUTION:
in minor or moderate injury.
NOTICE:
Indicates a hazardous situation which, if not avoided, could result
Indicates a hazardous situation which, if not avoided, could result
Indicates a situation which, if not avoided, could result in property
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Introduction 5
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 ser vice
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 specied for this product and certied 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.
• Conrm 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 aect 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.
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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, 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.
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Overview and Operation 7
Section 2: Overview and Operation
Description of the SpotOn temperature monitoring system .............................................. 7
How does it work? ................................................................................... 8
Setting up the SpotOn control unit .................................................................... 9
Instructions for use ................................................................................. 10
Transferring the patient and sensor ................................................................... 11
Removing the sensor ................................................................................ 11
To change temperature unit display (Celsius to Fahrenheit) .............................................12
Description of the SpotOn temperature monitoring system
e SpotOn temperature monitoring system measures the core temperature of the patient. e 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.
Power Supply
Sensor Cable
English 202052A
Monitor Cable
3M™ SpotOn
Control Unit
P
A
T
Sensor Connector
Figure 2: SpotOn Temperature Monitoring System
S
N
E
S
I
E
T
N
™
R
O
Temperature Sensor
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8 Overview and Operation
How does it work?
e SpotOn temperature monitoring system uses zero-heat-ux thermometry to accurately measure a person’s core
temperature as characterized in Figure 3 below. 1) e SpotOn temperature monitoring system gently warms the
sensor creating an isothermal zone under the sensor. 2) Once equilibrated to the core temperature, skin-surface
heat loss to the environment is prevented and a zero-heat-ux 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 zone development
3) Equilibrated - isothermal zone established
Figure 3: Isothermal tunnel formation with zero-heat-flux technology
SpotOn control unit
e SpotOn control unit displays noninvasive core temperature measurements obtained from the SpotOn
temperature sensor. e 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, 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. e 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
e SpotOn sensor is constructed of two layers of medical grade foam and a exible circuit which contains a
resistive warming circuit, two calibrated thermistors, and nonvolatile memory. e information that generates the
temperature trend graph is stored on the SpotOn sensor. If the patient is transferred from one location to another,
the SpotOn sensor is disconnected from the SpotOn sensor cable so the sensor is le in place on the patient. e
SpotOn sensor may be reconnected to a dierent 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.
e act of disconnecting and reconnecting the SpotOn sensor from the sensor cable is indicated by a gap in the
temperature trend graph.
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Overview and Operation 9
Back of Control Unit
To view information and connections on the back of the control unit, assure that controller is viewed
from a distance no further than 15” (38 cm) from the operator.
Digital Port
(used by 3M personnel only)
Stand Knob
°C/°F Temperature
Display Button
Monitor Cable Port
Figure 5: Back of Control Unit
e digital port is used only by 3M Patient Warming personnel for testing purposes and to access
variables within the control unit.
e 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.
Power Input Port
Front of Control Unit
Figure 6: Front of Control Unit
Setting up the SpotOn control unit
1. e SpotOn control unit must be properly installed and mounted by qualied personnel.
NOTE: e SpotOn sensor and control unit are suitable for use in the patient environment.
2. Connect the power supply to the back of the SpotOn control unit (see Figure 5: Back of Control
Unit).
Plug the power supply into an appropriate outlet. e standby screen will illuminate.
3. Connect the SpotOn sensor cable to the front of the control unit. See Figure 6: Front of Control
Unit for proper orientation and connection.
4. If desired, use the provided monitor cable to connect the SpotOn control unit to the patient
monitor
(see Figure 5: Back of Control Unit).
NOTE: Temperature input on patient monitor typically labelled T1 or T2.
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10 Overview and Operation
Instructions for use
1. Ensure the SpotOn system power supply is
connected to the back of the control unit and
the power supply is plugged into an appropriate
outlet. If desired, ensure the provided monitor
cable is connected to the back of the SpotOn
control unit and to the YSI-400 type input on the
patient monitor.
2. Use an alcohol wipe to clean and disinfect the
patient’s forehead above the orbita l ridge. Allow
the patient’s forehead to completely dry.
3. Connect the SpotOn temperature sensor to the
sensor cable connector. Ensure the sensor tab
is properly connected and is fully inserted into
the sensor cable (Figure 7). e display on the
control unit will change to the ready screen (See
“Ready” on page 14) once it conrms the sensor
connection.
Figure 7: Connect the sensor to the
sensor cable
Sensor Tab
4. Remove backing liners on the SpotOn temperature
sensor to expose adhesive (Figure 8).
5. Position the sensor cable away from the patient’s
face and apply the SpotOn temperature sensor
to the patient’s forehead above the orbital ridge
(Figure 9).
English 202052A
Figure 8: Remove the backing liners
Figure 9: Apply the SpotOn sensor to the
patient’s forehead
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Overview and Operation 11
6. Gently press the edge of the sensor to ensure good adhesion with the skin.
OPTIONAL: Support the SpotOn temperature sensor cable with the provided sensor cable clip.
7. e control unit will sense patient attachment aer several seconds and the control unit display will
change to the equilibration screen (see “Equilibration” on page 14).
8. e patient’s temperature will display on the patient monitor once equilibrium is reached
(approximately three minutes).
Transferring the patient and sensor
1. Prior to moving the patient, disconnect the sensor cable from the SpotOn sensor. e sensor may be
le on the patient and reconnected to another SpotOn system once patient transfer is complete.
NOTE: e SpotOn temperature sensor contains integrated memory that captures up to two hours
of temperature data in ve minute intervals. e SpotOn sensor will retain these temperatures and
hi st or y.
2. Carefully reconnect a SpotOn sensor cable and control unit to the temperature sensor once transfer is
complete.
3. e control unit will sense patient attachment aer several seconds and the control unit display will
change to the equilibration screen (see “Equilibration” on page 14).
4. e patient’s temperature will display on the patient monitor once equilibrium is reached
(approximately three minutes).
Removing the sensor
1. Disconnect the sensor cable from the SpotOn temperature sensor.
Disconnect the sensor cable clip from the bed or sheet,
if used.
2. Starting at the edge of the
SpotOn sensor, gently remove
the SpotOn temperature sensor
from the patient (Figure 10).
NOTE: Do not use the sensor
tab to remove the SpotOn
temperature sensor from the
patient.
NOTE: If needed, use an alcohol
swab along the sensor edge to
help remove the sensor from the
patient.
3. Discard the SpotOn sensor
and clean the sensor cable. (See
Section 5: General Maintenance
for details).
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Figure 10: Remove the sensor
Sensor
Tab
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12 Overview and Operation
To change temperature unit display (Celsius or Fahrenheit)
e SpotOn control unit can display temperature measurements in either Celsius or Fahrenheit. e unit
will be factor y preset to Celsius.
1. Plug the SpotOn control unit into an appropriate outlet.
2. Push the temperature display button on the back of the control unit to change to the desired
measurement scale.
NOTE:
e trend display is always shown in Celsius.
°C/°F Temperature
Display Button
Figure 11: Temperature Display Button
Shutting down the control unit
e plug on the power supply serves as the disconnect device. Turn the control unit on and o by
plugging or unplugging the power supply from the wall outlet. e power outlet shall be as close as
practical and shall be easily accessible.
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Display Panel 13
Section 3: Display Panel
Display screens ..................................................................................... 13
Sta rt-up ............................................................................................ 13
Standby ............................................................................................ 13
Ready .............................................................................................. 14
Equilibration ...................................................................................... 14
Running ........................................................................................... 14
Control unit error ................................................................................... 14
Sensor error ........................................................................................ 14
Display screens
Start-up
e start-up screen displays for approximately ve seconds
when the control unit is initially powered ON. e revision
number of the control unit soware is also displayed.
Standby
e SpotOn system graphic is displayed when the unit is not
in use.
English 202052A
FW-x.x.xxx
™
3M™ SpotOn
Temperature Monitoring System
TM
36 9
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14 Display Panel
Ready
e 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. e SpotOn sensor is now ready to be
attached to the patient.
SN - 000000000
Equilibration
A ashing yellow temperature display indicates the
sensor has been connected to the patient and to the
control unit and is in the process of equilibration.
e graph below the temperature output indicates
the progress of equilibration. is process will take
approximately three minutes.
If you see a temperature in the upper le hand corner
of the screen, that is the last recorded temperature that
has been captured by the sensor on the patient’s head.
e sensor captures and records a temperature every
ve minutes.
Aer the equilibration is complete, the patient’s body
temperature 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
36 0
39
37
35
C
Running
e running screen displays the deep tissue
temperature of the patient in white. e trend graph
at the bottom of the screen displays the last two hours
of the patient’s temperature in ve minute increments.
e bars on the graph will begin lling from the right
with the 36°C always visible. e blue bars indicate
that the temperature dropped below 36°C (white
indicates the temperature is above 36°C).
Control unit error
e SpotOn control unit error screen displays when
there is a system error. Discontinue use of unit.
Contact a biomedical technician.
Sensor error
e sensor error screen displays when there is a
temperature sensor or cable error. See “Section 4:
Troubleshooting” on page 15 for details.
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E- xx
E- xx
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Troubleshooting 15
Section 4: Troubleshooting
On Mode .......................................................................................... 15
Displays ........................................................................................... 15
Errors ............................................................................................. 16
e following conditions are listed in the order of which troubleshooting actions should be performed.
On Mode
Condition Cause Action
Unit does not power up. Unit is not plugged in, or power supply
is not plugged into an appropriate
outlet.
Unit failure. Contact 3M Patient Warming technica l
Make su re the power supply is plugged into
the control unit. Make sure the control unit
is plugged into an appropriate power outlet.
service.
Displays
Condition Cause Action
“Ready” screen continues to d isplay
while sensor is ad hered to the patient.
SN - 000000000
“Running” screen does not appear on
the control unit.
Sensor not properly adhered to the
patient.
Low patient temperat ure
(below 29 °C).
Control u nit fai lure. Discontinue use of unit. Contact 3M Pat ient
Control u nit may still be equilibrating. Wait unti l the SpotOn control unit has
Control u nit fai lure. Contact 3M Patient Warming technica l
Make su re the sensor is connected to t he
patient.
Press and hold the °C/°F button on the back
of the control unit for ve seconds to force
the control unit into equilibration mode. e
patient’s temperature wil l then display.
Warming technical service.
nished equilibration. Continue use.
service.
Patient temperature does not appear
on the patient monitor.
C
36 9
36 0
39
37
35
e patient ’s temperature output on
the control unit and patient monitor
does not read the same value.
English 202052A
C
Control u nit may still be equilibrating. Wait unti l the SpotOn control unit has
nished equilibration. Continue use.
Monitor cable is not plugged in. Make sure the monitor cable is plugged into
the control unit and patient monitor.
Cable failure. • Replace monitor cable.
• Contact 3M Patient War ming technical
service.
Control u nit fai lure. Contact 3M Patient Warming technica l
service aer use.
Cable failure. • Replace monitor cable.
• Contact 3M Patient War ming technical
service.
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16 Troubleshooting
Errors
Error Screen Condition Cause Action
E-1 through E-16, E-18
through E-99
E-xx
E-17 Sensor failure. Replace sensor.
E-xx
E-100 and up Control unit failure. Discontinue u se of the unit. Cont act a
E-xx
Sensor not properly
connected to the sensor
Make su re the sensor is connected to t he
sensor cable.
cable.
Sensor failure. Replace sensor.
Cable failure. • Replace sensor cable.
• Contact 3M Patient War ming technical
service.
Cable failure. • Replace sensor cable.
• Contact 3M Patient War ming technical
service.
Control u nit fai lure. Discontinue use of the unit. Contac t a
biomedical technician.
biomedical technician.
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General Maintenance 17
Section 5: General Maintenance, Storage and Service
Cleaning and Disinfecting Procedure .................................................................17
Storage ............................................................................................. 17
Service ............................................................................................. 17
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 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 so 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 so cloth.
Disinfecting the sensor cable
1. Clean the devices as described above.
2. Wipe down the control unit and cable using a damp so cloth and 70% isopropyl alcohol
solution. Avoid getting liquid into electronic ports.
3. Dry with a separate so 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 1-800-733-7775 for service information. Testing of the SpotOn
system can be performed by 3M Patient Warming or call Customer Service for information about
specic test procedures.
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18 General Maintenance
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Technical Service and Order Placement 19
Section 6: Technical Service and Order Placement
When you call for technical support ................................................................. 19
Technical service and order placement ............................................................... 19
When you call for technical support
Remember, we will need to know the serial number, soware number and error code of your SpotOn control
unit when you call us. e serial number label is located on the back of the control unit. (e rmware
number displays on the control unit when the control unit is connected to a power outlet.)
Technical service and order placement
USA
TEL: +1-952-947-1200
+1-800 -733-7775
FAX: +1-952-947-1400
+1-800-775-0002
Outside of the USA
Contact your local 3M Patient Warming representative.
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20 Technical Service and Order Placement
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Specifications 21
Section 7: Specifications
Physical characteristics .............................................................................. 21
Electrical characteristics ............................................................................22
Temperature characteristics ......................................................................... 22
Performance characteristics ......................................................................... 22
Environmental conditions ........................................................................... 22
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, FIR E AND
MECHANICAL HAZARDS ONLY IN ACCORDANCE WITH UL 60601-1; CAN/CSA-C22.2,
No. 60601-1; ANSI/AAMI ES60601-1:2005 CSA-C22.2 No.601-1:08; EN60601-1; Control
No.4HZ8
Classied under IEC 60601-1 Guidelines (and other national versions of the Guidelines) as Class II, Type CF,
Debrillation-Proof, Ordinary Equipment. Conforms to EN12470. Not suitable for use in the presence of
ammable anesthetic mixtures with air or nitrous oxide.
Classied by Underwriters Laboratories Inc. with respect to electric shock, re, and mechanical hazards only,
in accordance with UL 60601-1, IEC 60601-1, and Canadian/CSA C22.2 No. 601.1. ANSI/AAMI ES 60601-1;
2005. EN60601-1. Classied 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 exible circuit
Recommended Calibration Check
Every 12 months
Sensor Shelf Life
36 months
Digital Port
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.
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22 Specifications
Electrical characteristics
External power supply
100-240 VAC, 50-60 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
3 minutes
Time response
Approximately three minutes
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 k Pa (12 PSI to 15 PSI)
Oxygen environment
e sensor only is suitable for use in the
presence of an oxygen enriched environment.
Measurement locations
Patient’s lateral forehead above the orbital
ridge
Measurement range
25°C - 43°C
Measurement readout
Celsius or Fahrenheit
Leakage current
CF classication. Meets leakage current
requirements in accordance with UL 60601-1
and EN60601-1.
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Made in the USA by 3M Health Care�
3M is a trad emark of 3M C ompany, used u nder licens e in Canada � SPOTO N is a tradem ark of Arizant Healthcare I nc�, used under
license in Canada� ©2013 Arizant Heal thcare Inc� All righ ts reser ved�
3M Deut schland GmbH, Health Care Business
Carl- Schurz-Str� 1, 41453 Neuss, Germany
3M Health Care, 2510 Conway Ave�, St� Paul, MN 55144 USA
TEL 800-228-3957 | www�spotontemperature�com
202052A 04/13
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