ENG – Translations of the IFU can be found using this QR code.
FRE – Les traductions de cette notice d’utilisation peuvent être retrouvées à l’aide de ce code QR.
GER – Übersetzungen dieses Handbuchs können über diesen QR-Code abgerufen werden.
ITL – Utilizzando questo codice QR, è possibile trovare le traduzioni delle Istruzioni per l’uso.
SPA – Las traducciones de este manual se pueden encontrar utilizando este código QR.
POR – Pode aceder às traduções das instruções de utilização através deste código QR.
DUT – Vertalingen van de handleiding zijn te vinden met behulp van deze QR-code.
GRK – ΜετηχρήσηαυτούτουκωδικούQRμπορείτεναβρείτεμεταφράσεις
τωνοδηγιώνχρήσης(IFU).
DAN – ScandenneQR-kodeforatndeoversættelserafdennebrugsvejledning.
SWE – Översättningar av den här guiden kan hittas med denna QR-kod.
FIN – Käyttöohjeen käännökset löytyvät tällä QR-koodilla.
POL – TłumaczeniategoprzewodnikamożnaznaleźćzapomocątegokoduQR.
NOR – OversettelseravdennebruksanvisningenkannnesvedåbrukedenneQR-koden.
Instructions for Use / Operator’s Manual
https://www.nonin.com/support/7500fo
P/N 115157-000-01 05/2023 13700 1st Avenue North, Plymouth, MN 55441-5443 USA nonin.com
Instructions for Use
Model 7500FO
REPEC
Warranty
The device warranty
is 3 years.
nonin.com/warranty
Symbol
Glossary
nonin.com/symbols
Compliance
This product complies
with ISO 10993.
Not made from
natural rubber latex.
MPS, Medical Product Service GmbH
Borngasse 20
D-35619 Braunfels, Germany
MedEnvoy Switzerland
Gotthardstrasse 28, 6302 Zug
Switzerland
REP
CH
Warnings (continued)
• Use this device only with power adapters supplied by Nonin Medical.
• This device turns off after approximately 30 minutes when in low battery mode.
• This device should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the device should be
observed carefully to verify normal operation.
• The battery pack must be installed at all times while the device is operating—even when operating on AC power. Do NOT use the device without
batteries.
• The use of accessories, sensors, and cables other than those listed in this manual may result in increased electromagnetic emission and/or
decreased immunity of this device.
• To comply with relevant product safety standards, ensure that all alarm volumes are set appropriately and are audible in all situations. Do not
cover or otherwise obstruct any speaker openings.
• Thebercableforthisdeviceisextremelysensitiveandmustbehandledwithcautionatalltimes.Donotuseadamagedsensor.
• Ensure that the routing of the sensor cable from the 7500FO device in the control/observation room to the MR room does not compromise the
RF shielding of the MR room. A proper wave guide for the sensor cable passage through the RF cage must be taken into account by the RF cage
builder during site planning, or created afterwards.
• PortableRFcommunicationsequipmentsuchascellphonesorradios(includingperipheralssuchasantennacablesandexternalantennas)
shouldbeusednocloserthan30cm(12inches)toanypartofthemedicalelectricalsystem,includingcablesspeciedbythemanufacturer.
Otherwise, degradation of the performance of this equipment could result.
Cautions
• This equipment complies with IEC 60601-1-2 for electromagnetic compatibility for medical electrical equipment and/or systems. This standard
is designed to provide reasonable protection against harmful interference in a typical medical installation. However, because of the proliferation
of radio-frequency transmitting equipment and other sources of electrical noise in healthcare and other environments, it is possible that high
levels of such interference due to close proximity or strength of a source might disrupt the performance of this device. Medical electrical
equipment needs special precautions regarding EMC, and all equipment must be installed and put into service according to the EMC information
speciedinthismanual.
• Whenmountingthemonitortoamobilepole,mountingthemonitorhigherthan1.5meters(5feet)ormountingmorethan2kilograms(4.5
pounds)ofequipmentontothepolemayresultintipping,damagetotheequipment,orinjury.
• If the device does not beep during the initialization sequence, the speaker may not be functioning properly. Discontinue use until the situation is
corrected by Nonin Technical Service.
• Review all limits to ensure they are appropriate for the patient.
• Setting alarm limits to extremes can render the alarm system useless.
• Do not simultaneously touch the accessible connector pins and the patient.
• This device is a precision electronic instrument and must be repaired by Nonin Technical Service. Field repair of the
• device is not possible. Do not attempt to open the case or repair the electronics. Opening the case may damage the device and void the
warranty.
• If this device fails to respond as described, discontinue use until the situation is corrected; contact Nonin Technical Service.
• Thesensormightnotworkoncoldextremitiesduetoreducedcirculation.Warmorrubthengertoincreasecirculation,orrepositionthe
sensor.
• Do not gas sterilize or autoclave this device.
• Batteries might leak or explode if used or disposed of improperly.
• This device has motion tolerant software that minimizes the likelihood of motion artifact being misinterpreted as good pulse quality. In some
circumstances, however, the device may still interpret motion as good pulse quality.
• Do not place liquids on top of this device.
• Do not immerse this device or sensors in any liquids.
• Do not use caustic or abrasive cleaning agents on the unit or sensors.
• Follow local, state and national governing ordinances and recycling instructions regarding disposal or recycling of the device and device
components, including batteries. Use only Nonin-approved battery packs.
• IncompliancewiththeEuropeanDirectiveonWasteElectricalandElectronicEquipment(WEEE)2002/96/EC,donotdisposeofthisproductas
unsorted municipal waste. This device contains WEEE materials; please contact your distributor regarding take-back or recycling of the device. If
you are unsure how to reach your distributor, please call Nonin for your distributor’s contact information.
• Topreventpotentiallossofmonitoringorinaccuratedata,removeanyobjectsthatmighthinderpulsedetectionandmeasurement(e.g.,blood
pressurecuffs).
• Iftheentirememoryislled,portionsoftheoldestrecordwillbeoverwrittenwhenanewrecordbegins.
• This device is designed to determine the percentage of arterial oxygen saturation of functional hemoglobin. Factors that may degrade pulse
oximeter performance or affect the accuracy of the measurement include the following:
• A functional tester cannot be used to assess the accuracy of a pulse oximeter monitor or sensor.
• AllpartsandaccessoriesconnectedtotheserialportofthisdevicemustbecertiedaccordingtoatleastIECStandardEN60950,IEC62368-1,
or UL 1950 for data-processing equipment.
• Operation of this device below the minimum amplitude of 0.3% modulation may cause inaccurate results.
• The two-minute alarm silence is automatically engaged at startup.
• Do not use the power supply if the integrity of the AC cord conductors or the outlet is in doubt.
• Failureofanetworkdatacoupling(serialcable/connectors)willresultinlossofdatatransfer.
©2023 Nonin Medical, Inc. All trademarks are the property of Nonin Medical, Inc. unless otherwise noted.
• Excessive ambient light • Improperly applied sensor • Carboxyhemoglobin
• Excessive motion • Incorrect sensor type • Methemoglobin
• Electrosurgical interference • Poor pulse quality • Dysfunctional hemoglobin
• Bloodowrestrictors(arterialcatheters,
bloodpressurecuffs,infusionlines,etc.)
• Venous pulsations • Articialnailsorngernailpolish
• Anemia or low hemoglobin concentrations • A sensor not at heart level
• Moisture in the sensor • Cardiogreen and other intravascular dyes • Residue(e.g.,driedblood,dirt,grease,oil)
in the light path
P/N 115157-000-01 05/2023 13700 1st Avenue North, Plymouth, MN 55441-5443 USA nonin.com
Instructions for Use
Model 7500FO
Thank you for trusting Nonin with your patients’ healthcare needs. We sincerely appreciate your
business. Please read your Operator’s Manual carefully and direct any further questions to a Nonin
Technical Service representative. If you would like to order products or check the status of a current
order, please contact Customer Service.
Indications for Use/Intended Use/Intended Purpose
The Nonin Model 7500FO Pulse Oximeter is a portable tabletop device indicated for use in simultaneously measuring, displaying, and recording
functionaloxygensaturationofarterialhemoglobin(SpO2)andpulserateofadult,pediatric,andinfantpatientsinaMagneticResonance(MR)environ-
ment. Testing was performed in MR conditional environments at 1.5T and 3T. It is intended for spot checking and/or continuous monitoring of patients
who are well or poorly perfused.
Warnings
• Do not operate this device with the oximeter or sensor connectors within the MR room. The oximeter and sensor connector should be positioned in
thecontrol/observationroomwiththeberopticcableandsensorenteringtheMRroomthroughthewall.
• Donotuseinanexplosiveatmosphereorinthepresenceofammableanestheticsorgases.
• ThisdeviceisnotdebrillationproofperIEC60601-1.
• The battery charger cannot be used in the MR environment.
• This device is intended only as an adjunct device in patient assessment. It must be used in conjunction with other methods of assessing clinical
signs and symptoms.
• Inspectthesensorapplicationsiteatleastevery4hourstoensurecorrectsensoralignmentandskinintegrity.Patientsensitivitytosensorsand/or
double-backed adhesive strips may vary due to medical status or skin condition.
• Avoid excessive pressure to the sensor application site as this may cause damage to the skin beneath the sensor.
• Oximeterreadingsofthisdevicemaybeaffectedbytheuseofanelectrosurgicalunit(ESU).
• To avoid patient injury, use only Nonin-branded PureLight® pulse oximeter sensors. These sensors are manufactured to meet the accuracy
specicationsforNoninpulseoximeters.Usingothermanufacturers’sensorscanresultinimproperpulseoximeterperformance.
• Topreventimproperperformanceand/orpatientinjury,verifycompatibilityofthemonitor,sensor(s),andaccessoriesbeforeuse.
• Nomodicationstothisdeviceareallowedasitmayaffectdeviceperformance.
• Do not use a damaged sensor. If the sensor is damaged in any way, discontinue use immediately and replace the sensor.
• Verify all alarm settings and limits during system startup to ensure that they are set as intended.
• Do not use this device in or around water or any other liquid, with or without AC power.
• As with all medical equipment, carefully route patient cables and connections to reduce the possibility of entanglement, strangulation, or injury to
the patient.
Contact Customer Service or Technical Service
TollFree:800.356.8874(U.S.andCanadaonly)
Phone: +1 763.553.9968
Email: [email protected]
Nonin Medical Inc.
13700 1st Avenue North
Plymouth,MN55441-5443,USA
Nonin B.V.
Doctor Paul Janssenweg 150
5026 RH Tilburg, Netherlands
Have other questions or want to learn more?
Visit nonin.com to read more about our history, product offerings, and more.
Nonin is committed to sustainable practices. This paper is made with
FSC-certiedmaterials,printedwithsoyink,andis100%recyclable.
For summary of safety and clinical data see above QR code.
7500FO Specications
*AdditionalspecicationsareavailableintheIFU/Operator’sManualthatcanbelocatedusingtheQRCode.
• Oxygen saturation measured from 0%-100% SpO2. With an accuracy typically ± 2 with a maximum of ± 3.
• Pulse rate measured from 18bpm-321bpm. With an accuracy data is typically ± 3 with a maximum of ± 5.
Measurement Wavelengths and Output Power:
• Red: 660 nanometers @ 0.8 mW maximum average
• Infrared: 910 nanometers @ 1.2 mW maximum average
To set up and use the Nonin Model 7500FO pulse oximeter, please
follow the simple instructions below.
Instructions for Use
Model 7500FO
P/N 115157-000-01 05/2023 13700 1st Avenue North, Plymouth, MN 55441-5443 USA nonin.com
Operating the Model 7500FO
1. Fully charge the battery pack, which takes approximately four hours.
2. PresstheON/STANDBYbutton.MakesureallLEDs(excepttheACPowerSupplyLED)light
up and the unit beeps three times during the startup sequence. If any LED is not lit, do not use
the device and contact Nonin Technical Service for assistance.
3. Insert the sensor into the Model 7500FO, then apply it to the patient and take the measure-
ment.Formoreinformationonhowtouseaspecicsensor,pleaserefertothatsensor’s
Operator’s Manual.
4. WhendoneusingtheModel7500FO,pressandholdtheON/STANDBYbuttonforonetothree
seconds to turn the device off.
Displays, Indicators, and Controls
P/N 115157-000-01 05/2023 13700 1st Avenue North, Plymouth, MN 55441-5443 USA nonin.com
Instructions for Use
Model 7500FO
Operator Functions
Please refer to the Operator’s Manual on nonin.com/support/7500fo
for troubleshooting guidance and more detailed operating instructions.
P/N 115157-000-01 05/2023 13700 1st Avenue North, Plymouth, MN 55441-5443 USA nonin.com
Instructions for Use
Model 7500FO
Operating Modes and Defaults
The Model 7500FO is shipped with factory defaults active. Refer to the Operator’s Manual for
moreinformationaboutitsothermodes,includingSetupmode,User-DenedDefaults,and
Patient Security mode.
Memory Features
The Model 7500FO can collect and store 70 hours of continuous SpO2 and pulse rate
information. Patient data is retained even when both external and battery power are lost.
For information on clearing patient memory or playing back memory data, please refer to
the Operator’s Manual.
Care and Maintenance
Clean the Model 7500FO separately from the sensors. Please refer to the sensor’s Operator’s
Manual for information on how to clean the sensors.
To clean the Model 7500FO:
1. Dampen a soft cloth with isopropyl alcohol, mild detergent, or a 10% bleach
(5.25%sodiumhypochlorite)withwatersolution.Donotpourorsprayanyliquidsonto
the Model 7500FO, and do not allow any liquid to enter any openings in the device.
2. Allow the unit to dry thoroughly before reusing it.
Field repair of the Model 7500FO circuitry is not possible. If the Model 7500FO is not func-
tioning properly, please reference the “Troubleshooting” section of the Operator’s Manual.
Error Codes
This device includes error codes that indicate problems with the unit. Error codes are
indicated by “Err” in the %SpO2 display, and a capital “E” followed by a 2-digit code in the
pulse rate display. To correct error conditions, perform the following steps:
1. Turn the unit off and then back on again to remove the error code.
2. If the error persists, disconnect all power, and then reconnect the power and turn
the unit back on.
If the error still persists, note the error code and contact Nonin Technical Service.
Alarm Bar
LED This LED indicates all alarm conditions.
Pulse Quality
LED
This amber LED blinks to indicate a poor pulse signal. If there is a sustained
period of poor-quality signals, this LED will display a steady, constant light.
Sensor Alarm
LED
This amber LED indicates when a sensor has become disconnected, has
failed, or is not compatible with this monitor.
Pulse Strength
Bargraph LED
Indicates pulse strength. The height of the Pulse Strength Bargraph LED is
proportional to the pulse signal, and the color is determined by pulse strength.
Alarm Silence
LED
When blinking, this amber LED indicates that the audible alarm is silenced
for two minutes. When alarms are active, this LED blinks in time with the
alarmbar.Ifnoalarmsareactive,thisLEDashesatthemediumpriority
alarm rate. When lit solid, the Alarm Silence LED indicates that audible alarm
volumesaresettolessthan45dB.
AC Power
Supply LED Glows green when connected to external power.
Low Battery
LED
This amber LED indicates a low battery charge when blinking, and a critical
battery charge when lit solidly.
On/Standby
Pulse Rate
Display
Alarm
Silence % SpO2
Display Alarm
Bar Speaker
Sensor
Connector
Plus(+) Minus(-) Limits
For more information on the displays, indicators, and controls, please refer to the
Operator’s Manual.
Function Button Instruction
Turn the Model
7500FO on and off
To turn on, press the ON/STANDBY button. To turn off, press and
hold the button for at least one second. In Patient Security mode,
hold the ON/STANDBY button for three seconds to turn off.
Initiate an event
marker Quickly press the ON/STANDBY button while the unit is on.
Temporarily mute the
audible alarms Press the Alarm Silence button.
Change pulse tone
volume
QuicklypressthePlus(+)buttonwhiletheunitisinoperating
mode. Press again to sequence through volume options for
pulse tones.
Set alarm limits or
alarm volumes, clear
memory or set clock
Quickly press the Limits button to step through the Limits menu.
Use the Plus or Minus buttons to adjust alarm limits or selected
volumes as desired.
Then Or
Refer to the Operator’s Manual for more information about advanced options, which are only
recommended for trained operators.
Parameter Factory Default
SpO2 High Alarm Limit Off
SpO2 Low Alarm Limit 85%
Pulse Rate High Alarm Limit 200 BPM
Pulse Rate Low Alarm Limit 50 BPM
Alarm Volume High
Oximetry Averaging Standard/Fast Averaged SpO2(no)
Alarms and Limits
Audio and visual alarms alert you about product malfunctions or changing patient conditions.
Alarm Indicated By What It Means
High priority alarm
Rapidly-blinking red Alarm
Bar LED and a red Pulse
Strength Bargraph LED
Immediate patient attention is required.
Medium priority
alarm
Slowly-blinking amber
Alarm Bar LED
There may be problems with the equipment, or a
non-life-threatening change in patient condition.
Watchdog alarm Loud, two-tone,
steadily-beeping signals Hardware of software malfunction.
Informational tone Single beeps or series of
three beeps
Communicating important information, such as
startup/initialization.
To silence an alarm for two minutes, press the Alarm Silence button.
Clinical Benets
Nonin pulse oximeters allow for the management of patients’ medical conditions by providing fast, accurate, real-time,
noninvasive oxygen measurement in order to meet patients’ medical needs.
Adverse Event Statement
Users and/or patients should report adverse events involve their Nonin device to Nonin Medical, Inc. and the
competent authority of the EU Member State in which the user and/or patient is established, if applicable.
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