Nonin Onyx Vantage 9590 User manual

8339-001-07
© 2019 Nonin Medical, Inc.
MPS, Medical Product Service GmbH
Borngasse 20
D-35619 Braunfels, Germany
Nonin and Onyx are registered trademarks of Nonin Medical, Inc.
U.S. Patents 5,490,523; 5,792,052
EC
REP
Nonin Medical, Inc.
13700 1st Avenue North
Plymouth, Minnesota 55441 USA
[phone] (outside US and Canada)
+ 31 (0)13 - 79 99 040 (Europe)
[phone] (US and Canada)
Fax: [phone]
+31 (0)13 - 79 99 042 (Europe)
E-mail: [email protected]
[email protected] (Europe)
nonin.com
Instructions for Use—English
Onyx®Vantage 9590 Finger Pulse Oximeter
Indications for Use
The Nonin®Onyx Vantage 9590 Finger Pulse Oximeter is a small, lightweight, portable device indicated for use in measuring
and displaying functional oxygen saturation of arterial hemoglobin (%SpO2) and pulse rate of patients who are well or poorly
perfused. It is intended for spot-checking of adult and pediatric patients on digits (fingers, thumb, toes) that are between 0.3–
1.0 inch (0.8 – 2.5 cm) thick. The device’s intended use environments include hospitals, clinics, long-term care facilities,
skilled nursing facilities, emergency medical services, and home healthcare services.
CAUTION: Regulatory authorities outside the U.S. recognize the use of this device in motion conditions.
Warnings
• Do not use the device in an MR environment, in an explosive atmosphere, or on neonatal patients.
• This device is not defibrillation proof per IEC 60601-1.
• Inspect the sensor application site at least every 4 hours to ensure correct sensor alignment and skin integrity. Patient sensitivity to
the sensor 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.
• This device is intended only as an adjunct in patient assessment. It must be used in conjunction with other methods of assessing
clinical signs and symptoms.
• The device must be able to measure the pulse properly to obtain an accurate SpO2measurement. Verify that nothing is hindering the
pulse measurement before relying on the SpO2measurement.
• Operation of this device below the minimum amplitude of 0.3% modulation may cause inaccurate results.
• General operation of the device may be affected by the use of an electrosurgical unit (ESU).
• 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.
• Keep the oximeter away from young children. Small items such as the battery door, battery, and lanyard are choking hazards.
• Certain activities may pose a risk of injury, including strangulation, if lanyard should become wrapped around your neck.
• Before changing batteries, make sure the device is off and is not applied to a digit.
• Portable RF communications equipment such as cell phones or radios (including peripherals such as antenna cables and external
antennas) should be used no closer than 30 cm (12 inches) to any part of the ME system, including cables specified by the
manufacturer. Otherwise, degradation of the performance of this equipment could result.
Cautions
• This device has no audible alarms and is intended only for spot-checking.
• 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:
• The device may not work when circulation is reduced. Warm or rub the finger, or re-position the device.
• This device’s display will go blank after 30 seconds of no readings or poor readings.
• In some circumstances, the device may interpret motion as good pulse quality. Minimize patient motion as much as possible.
• Clean the device before applying it to a patient.
• Do not sterilize, autoclave, or immerse this device in liquid. Do not pour or spray any liquids onto the device.
• Do not use caustic or abrasive cleaning agents, or any cleaning agent containing ammonium chloride.
• 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.
• A flexible circuit connects the two halves. Do not twist or pull the flexible circuit or overextend the device’s spring. Do not hang the
lanyard from the device’s flexible circuit.
• A functional tester cannot be used to assess the accuracy of a pulse oximeter monitor.
• 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 specified in this manual.
• Batteries may leak or explode if used or disposed of improperly. Remove batteries if the device will be stored for more than 30 days.
Do not use different types of batteries at the same time. Do not mix fully charged and partially charged batteries at the same time.
These actions may cause the batteries to leak.
• Follow local, state, and national governing ordinances and recycling instructions regarding disposal or recycling of the device and
device components, including batteries.
• In compliance with the European Directive on Waste Electrical and Electronic Equipment (WEEE) 2002/96/EC, do not dispose of this
product as 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.
• When using the device in the home, avoid exposing the device to lint and dust.
%SpO
2
!
• do not apply the pulse oximeter on the
same arm as a blood pressure cuff,
arterial catheter or infusion line(s) (IVs)
• excessive light, such as sunlight or direct
home lighting
• excessive motion
• moisture in the device
• improperly applied device
• finger is outside recommended size
range
• poor pulse quality
• venous pulsations
•
anemia or low hemoglobin concentrations
• cardiogreen and other intravascular dyes
• carboxyhemoglobin
• methemoglobin
• dysfunctional hemoglobin
• artificial nails or fingernail polish
• residue (e.g., dried blood, dirt, grease, oil)
in the light path

2
Symbols
Installing Batteries
Two 1.5 volt AAA-size batteries power the 9590 for about 6,000 spot checks or 36 hours of operation. Nonin recommends
using alkaline batteries (included with each new device). When batteries are low, the numeric displays flash once per second.
Remove batteries if the device will be stored for more than 30 days. Replace low batteries as soon as possible, using the
instructions below.
WARNING: Before changing batteries, make sure the device is off and is not applied to a digit.
NOTE: Rechargeable batteries may be used; however, they require more frequent replacement.
1. Hold the 9590 as shown in figure A. To release the device’s battery tray, press upward and then pull outward slightly with
the thumb.
2. Remove the old batteries from the battery tray. Dispose of the batteries properly.
3. Insert two new 1.5 volt AAA-size batteries. Follow the polarity markings (+ and -) as illustrated in figure B. Proper
positioning of the batteries is essential for operation.
4. Carefully guide the battery tray back onto the device. Press downward and then push inward slightly to re-secure the
battery tray (figure C). Do not force it into place; it fits only when properly positioned.
5. Insert your finger into the device to verify operation. See the Activating the Onyx Vantage 9590 and Verifying Operation
section for more information.
Symbol Description Symbol Description
!
Caution! SN Serial number
Follow Instructions for Use
REF
REF
Catalogue number
EC
REP
Authorized Representative in the European
Community
QTY
QTY
Quantity
CE Marking indicating conformance to
EC Directive No. 93/42/EEC concerning
medical devices.
Manufacturer
US
Country of manufacture
Type BF Applied Part (patient isolation from
electrical shock) Date of manufacture
Not for continuous monitoring
(no alarm for SpO2)IP33
Protected against spraying water and against
access to hazardous parts with a tool, per IEC
60529.
Battery orientation
Indicates separate collection for electrical
and electronic equipment (WEEE). Storage/shipping temperature range
UL Mark for Canada and the United States
with respect to electric shock, fire, and
mechanical hazards only in accordance
with:
• ANSI/AAMI ES60601-1:2005/(R)2012
and CAN/CSA-C22.2 No. 60601-1:14
• ISO 80601-2-61:2011
Non-ionizing electromagnetic radiation.
Equipment includes RF transmitters; interference
may occur in the vicinity of equipment marked
with this symbol.
RoHS compliant (China)
Federal law (USA) restricts this device to sale by
or on the order of a licensed practitioner.
A
BC

3
Activating the Onyx Vantage 9590 and Verifying Operation
The device contains numeric Light-Emitting Diodes (LEDs) that display oxygen saturation and pulse rate. A tricolor LED
display (pulse quality indicator, shown at left) provides a visual indication of the pulse signal quality, while blinking at the
corresponding pulse rate. This display changes colors to alert you to changes in pulse quality that may affect the readings:
• Green indicates a good pulse signal.
• Yellow indicates a marginal pulse signal.
• Red indicates an inadequate pulse signal.
Activate the 9590 by inserting the patient’s finger into the device. The device detects the inserted finger and automatically
illuminates the displays. Correct positioning of the device on the finger is critical for accurate measurements.
NOTE: While on the finger, do not press the device against any surface and do not squeeze or hold it together. The internal
spring provides the correct pressure; additional pressure may cause inaccurate readings.
1. Insert the patient’s finger, nail side up, into the 9590 until the fingertip touches the built-in stop guide.
2. Make sure the finger is lying flat (not on its side) and is centered within the device. For best results, keep the device at
the patient’s heart or chest level.
3. If the device does not turn on, remove the finger and wait a few seconds before reinserting it.
When a finger is inserted, the device performs a brief startup sequence. Verify that all LEDs illuminate during the startup
sequence. If any LED is not lit, do not use the 9590; contact Nonin Technical Service for repair or replacement.
After the startup sequence, the device begins sensing the pulse (indicated by the blinking pulse quality indicator). Allow the
device to stabilize and observe about 4 seconds of continuous green-colored pulse quality before relying on the displayed
values. Continually verify operation. It is common for the displayed values to fluctuate slightly over a period of several
seconds. If the pulse quality indicator blinks yellow or red, try another finger.
A minus sign (-) appears in the left-most digit of the %SpO2display when the device senses the finger has been removed.
The last measured SpO2and pulse rate values display for 10 seconds while the device automatically turns off. The device
will automatically shut off (to conserve battery life) approximately 10 seconds after the finger is removed, or after a 2-minute
period of inadequate pulse signals.
If the 9590 does not turn on or if it shuts off unexpectedly:
• Verify batteries are correctly inserted. Note: If batteries are installed backwards, the unit will not function.
• The batteries are depleted. Replace batteries.
Continually verify operation. If the problem persists, remove the batteries and contact Nonin Technical Service.
The OxitestPlus7 by Datrend Systems, Inc. can be used to verify operation of the pulse oximeter.
Using the Lanyard
WARNING: Certain activities may pose a risk of injury, including strangulation, if lanyard should become
wrapped around your neck.
!
CAUTION: A flexible circuit connects the two halves. Do not twist or pull the flexible circuit or overextend the
device’s spring. Do not hang the lanyard from the device’s flexible circuit.
A lanyard is provided for convenience. The device will function with or without the lanyard.
If lanyard use is desired, thread the lanyard as shown below.
Pulse Quality
Indicator
%SpO
2

4
Onyx Vantage 9590 Care, Maintenance, and Cleaning
The advanced digital circuitry within the device requires no calibration or periodic maintenance other than battery
replacement. The device’s expected service life is 5 years. Field repair of the 9590 circuitry is not possible. Do not attempt
to open the case or repair the electronics. Opening the case will damage the device and void the warranty. Do not open the
9590 more than 90°, and do not twist or pull on the device when cleaning.
Cleaning the Onyx Vantage 9590
CAUTIONS:
!
• Clean the device before applying it to a patient.
• Do not sterilize, autoclave, or immerse this device in liquid. Do not pour or spray any liquids onto the device.
• Do not use caustic or abrasive cleaning agents, or any cleaning agent containing ammonium chloride or isopropyl alcohol.
1. To clean, wipe the surfaces with a soft cloth dampened with mild detergent or a 10% bleach solution or equivalent.
(household bleach [5.25% sodium hypochlorite]). Do not use undiluted bleach or any cleaning solution other than those
recommended here, as permanent damage could result.
2. Dry with a soft cloth, or allow to air dry. Ensure that all surfaces are completely dry.
Equipment Response Time
If the signal from the sensor is inadequate, the last measured SpO2and pulse rate values
freeze for 10 seconds and are then replaced with dashes.
Example: SpO2Exponential Averaging
SpO2decreases 0.75% per second; pulse rate = 75 BPM
The response of the 4-beat average is 1.5 seconds.
Testing Summary
SpO2accuracy and low perfusion testing was conducted by Nonin Medical, Inc. as described below.
SpO2Accuracy Testing
At an independent research laboratory, SpO2accuracy testing is conducted during induced hypoxia studies on healthy, male
and female, non-smoking, light-to-dark-skinned subjects that are aged 18 years and older. The measured arterial hemoglobin
saturation value (SpO2) of the device is compared to arterial hemoglobin oxygen (SaO2) value, determined from blood
samples with a laboratory co-oximeter. The accuracy of the device is in comparison to the co-oximeter samples measured
over the SpO2range of 70–100%. Accuracy data is calculated using the root-mean-squared (Arms value) for all subjects, per
ISO 80601-2-61 and ISO 9919, Standard Specification for Pulse Oximeters for Accuracy.
Low Perfusion Testing
This test uses an SpO2Simulator to provide a simulated pulse rate, with adjustable amplitude settings of various SpO2levels.
The device must maintain accuracy in accordance with ISO 80601-2-61 and ISO 9919 for pulse rate and SpO2at the lowest
obtainable pulse amplitude (0.3% modulation).
Performance in Motion
Motion artifact simulation introduced by a pulse oximeter tester determines whether the oximeter meets the criteria of
ISO 80601-2-61 and ISO 9919 for pulse rate during simulated movement, tremor, and spike motions.
Contact [email protected] for more information regarding motion testing.
Principles of Operation
Pulse oximetry is a non-invasive method that passes red and infrared light through perfused tissue and detects the fluctuating
signals caused by arterial pulses. Well-oxygenated blood is bright red, while poorly oxygenated blood is dark red. The pulse
oximeter determines functional oxygen saturation of arterial hemoglobin (SpO2) from this color difference by measuring the
ratio of absorbed red and infrared light as volume fluctuates with each pulse.
SpO2Values Average Latency
Standard/Fast Averages SpO24 beat exponential 2 beats
Pulse Rate Values Response Latency
Standard/Fast Averages Pulse Rate 4 beat exponential 2 beats
Equipment Delays Delay
Display Update Delay 1.5 seconds

5
Specifications
Oxygen Saturation Display Range: 0% to 100% SpO2
Pulse Rate Display Range: 18 to 321 beats per minute (BPM)
Declared Accuracy:
The tables below show Arms values measured using the Onyx Vantage 9590 in a clinical study in non-motion conditions.
NOTE: If your national regulatory authority recognizes accuracy in motion, please contact [e-mail] for accuracy data.
SpO2Low Perfusion Accuracy (Arms*) 70 to 100% ±2 digits
Pulse Rate Declared Accuracy Range (Arms*): 20 to 250 BPM ±3 digits
Low Perfusion Pulse Rate Declared Accuracy Range (Arms*): 40 to 240 BPM ±3 digits
Measurement Wavelengths and Output Power**:
Red: 660 nanometers @ 0.8 mW maximum average
Infrared: 910 nanometers @ 1.2 mW maximum average
Temperature:
Operating: 23 °F to 104 °F / -5 °C to 40 °C
Storage/Transportation: -40 °F to 158 °F / -40 °C to 70 °C
Time (from storage) for monitor to be ready for its intended use: 3 minutes to warm from -40 °C to -5 °C
5 minutes to cool from 70 °C to 40 °C
Humidity:
Operating: 10% to 90% non-condensing
Storage/Transportation: 10% to 95% non-condensing
*± 1 Arms represents approximately 68% of measurements at zero bias.
**This information is especially useful for clinicians performing photodynamic therapy.
Accuracy Summary by Decade – Finger and Thumb Accuracy Summary by Decade – Toe
Decade Oxygen Saturation (Arms) Decade Oxygen Saturation (Arms)
70 – 80% ±2 70 – 80% ±2
80 – 90% ±2 80 – 90% ±3
90 – 100% ±2 90 – 100% ±3
70 – 100% ±2 70 – 100% ±3
This graph shows plots of the error (SpO2– SaO2)
by SaO2using the 9590 with a linear regression fit
and upper 95% and lower 95% limits of agreement.
Each sample data point is identified by subject
from a clinical study in non-motion conditions.
This graph shows plots of the error (SpO2– SaO2)
by SaO2using the 9590 with a linear regression fit
and upper 95% and lower 95% limits of agreement.
Each sample data point is identified by subject from
a clinical study using toes in non-motion conditions.

6
Altitude:
Operating: Up to 13,123 feet / 4,000 meters
Hyperbaric Pressure: Up to 4 atmospheres
Battery Life:
Operating: Approximately 6,000 spot checks or 36 hours of continuous operation
using new alkaline batteries.
Storage: 12 months
Classifications per ANSI/AAMI ES60601-1 / CAN/CSA-C22.2 No. 60601-1:
Degree of Protection: Type BF-Applied Part
Enclosure Degree of Ingress Protection: IP33
Mode of Operation: Continuous
This product complies with ISO 10993-1, Biological evaluation of medical devices – Part 1: Evaluation and testing.
This device is not made with natural rubber latex.
Warranty
NONIN MEDICAL, INCORPORATED, (Nonin) warrants to the purchaser, for a period of 4 years from the date of purchase,
each Onyx Vantage 9590 exclusive of the batteries, spring, lanyard, and lanyard lock.
Nonin shall repair or replace any Onyx Vantage 9590 found to be defective in accordance with this warranty, free of charge,
for which Nonin has been notified by the purchaser by serial number that there is a defect, provided notification occurs within
the applicable warranty period. This warranty shall be the sole and exclusive remedy by the purchaser hereunder for any
Onyx Vantage 9590 delivered to the purchaser which is found to be defective in any manner whether such remedies be in
contract, tort or by law.
This warranty excludes cost of delivery to and from Nonin. All repaired units shall be received by the purchaser at Nonin’s
place of business. Nonin reserves the right to charge a fee for a warranty repair request on any Onyx Vantage 9590 found
to be within specifications.
Onyx Vantage 9590 is a precision electronic instrument and must be repaired by trained Nonin personnel only. Any sign or
evidence of opening the Onyx Vantage 9590, field service by non-Nonin personnel, tampering, or any kind of misuse of the
Onyx Vantage 9590, shall void the warranty. All non-warranty work shall be done at Nonin’s standard rates and charges in
effect at the time of delivery to Nonin.
nonin.com
Nonin Medical, Inc.
13700 1st Avenue North
Plymouth, Minnesota 55441 USA
[phone] (USA and Canada)
[phone] (outside USA and Canada)
Fax [phone]
E-mail: [email protected]
Nonin Medical B.V.
Prins Hendriklaan 26
1075 BD Amsterdam, Netherlands
+31 (0)13 - 79 99 040 (Europe)
Fax: +31 (0)13 - 79 99 042
E-mail: [email protected]

7
WARNING: Portable RF communications equipment such as cell phones or radios (including peripherals such as antenna cables
and external antennas) should be used no closer than 30 cm (12 inches) to any part of the ME system, including cables specified by
the manufacturer. Otherwise, degradation of the performance of this equipment could result.
Manufacturer’s Declaration
Refer to the following tables for specific information regarding this device’s compliance to IEC 60601-1-2.
Essential Performance
Essential performance of the 9590 is defined as SpO2accuracy and pulse rate accuracy or an indication of abnormal
operation. Accuracies may be affected as a result of exposure to electromagnetic disturbances that are outside of the
environments listed in the Indications For Use. If issues are experienced, move the Nonin system away from the source of
electromagnetic disturbances.
Table 1: Electromagnetic Emissions
Emissions Test Compliance
This device is intended for use in the electromagnetic environment specified below.
The customer and/or user of this device should ensure that it is used in such an environment.
RF Emissions
CISPR 11 Group 1
RF Emissions
CISPR 11 Class B
Table 2: Electromagnetic Immunity
Immunity Test Compliance
Electrostatic Discharge (ESD)
IEC 61000-4-2
±8 kV contact
±15 kV air
Power Frequency (50/60 Hz) Magnetic Field
IEC 61000-4-8 30 A/m
Radiated RF
IEC 61000-4-3
80 MHz – 2.7 GHz 10 V/m
380 – 390 MHz 27 V/m
430 – 470 MHz 28 V/m
704 – 787 MHz 9 V/m
800 – 960 MHz 28 V/m
1.7 – 1.99 GHz 28 V/m
2.4 – 2.57 GHz 28 V/m
5.1 – 5.8 GHz 9 V/m
Table 3: Not Applicable
Harmonic Emissions (IEC 61000-3-2), Voltage Flicker Emissions (IEC 61000-3-3), Electrical Fast Transients (IEC 61000-4-
4), Surge (IEC 61000-4-5), Voltage dips (IEC 61000-4-11), Conducted Immunity (IEC 61000-4-6)
NOTE: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects, and people.