INSIGNIA NS-PSOXMW1 Quick Setup Guide

QUICK SETUP GUIDE

FEATURES

• Attaches painlessly to your nger and measures your oxygen levels and heart rate without the use of needles

• Digital display shows your results in a clear and easy-to-read format

• Compact size for easy storage and transportation

• 10 brightness levels let you read the display in dark environments

PRODUCT OVERVIEW

Top Vi ew

Low battery indicator

Oxygen saturation

Pulse rate

Power Button

Pulse Oximeter with Digital Display

NS-PSOXMW1

Before using your new product, please read these instructions to prevent any damage.

PACKAGE CONTENTS

• Pulse Oximeter

• Lanyard

• AAA batteries (2)

• Quick Setup Guide

Pulse bar

Bottom View

Battery cover

Hanging hole

INSTALLING THE BATTERIES

When the battery indicator is blinking, replace the batteries.

1 Slide the battery cover o.

2 Insert two AAA batteries into the

compartment. Make sure that the + and – signs in the compartment match the batteries.

3 Replace the battery cover.

Note: Remove the batteries if your pulse oximeter will

not be used for long periods of time.

TAKING A READING

Note: This device is not intended to diagnose or treat any

medical condition or disease. It is intended for non-medical use by healthy people to monitor their pulse rates and blood oxygen levels. It is for sports and aviation use only. People who need SpO2 and pulse rate measurements because of a medical condition should not use this pulse oximeter and should consult with their physician.

1 Clean the nger being tested with alcohol before

and after each test.

2 Squeeze the end of your pulse oximeter and

insert a nger into the opening.

3 Press the power button to turn on your pulse

oximeter.

4 Keep your nger, hand, and body still while your

pulse oximeter takes a reading. The display shows your oxygen saturation and pulse rate.

5 When you're nished, remove your nger. Your

pulse oximeter turns o automatically when there is no signal for eight seconds.

USING YOUR PULSE OXIMETER

Changing the brightness

Turn on the pulse oximeter, then press and hold the power button to adjust the display's brightness. There are 10 brightness levels. The default is level four.

Changing the display mode

Turn on the pulse oximeter, then press the power button to change how the readings are displayed. There are four display modes:

Attaching the lanyard 1 Thread the lanyard through the hanging hole,

then pull the lanyard through the smaller loop. 2 Thread the thick end of the lanyard through the threaded end before pulling it tight.

WARNINGS:

• Keep your oximeter away from young children. Small items such as

the battery cover, batteries, and lanyard are choking hazards.

• The lanyard that is tied to the oximeter may cause strangulation

due to excessive length.

SAFETY INFORMATION

• Carefully read all the provided information before use.

• Operation of the ngertip pulse oximeter may be aected by the use of an electrosurgical unit (ESU).

• The ngertip pulse oximeter must be able to measure the pulse properly to obtain an accurate SpO2 measurement. Make sure that nothing is hindering the pulse measurement before relying on the SpO

measurement.

• Do not use the ngertip pulse oximeter in an MRI or CT environment.

• Do not use the ngertip pulse oximeter in situations where alarms are required. The device has no alarms. It is not for continuous monitoring.

• Do not use the ngertip pulse oximeter in an explosive atmosphere.

• The ngertip pulse oximeter is intended only as an adjunct in patient assessment. It must be used in conjunction with other methods of assessing clinical signs and symptoms.

• In order to ensure correct sensor alignment and skin integrity, the maximum application time at a single site for our device should be less than half an hour.

• Do not sterilize the device using autoclaving, ethylene oxide sterilizing, or immersing the device in liquid. The device is not intended for sterilization.

• Follow local ordinances and recycling instructions regarding disposal or recycling of the device and device components, including batteries.

• This equipment complies with IEC 60601 1 2:2014 for electromagnetic compatibility for medical electrical equipment and/or systems. 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.

• Portable and mobile RF communications equipment can aect medical electrical equipment.

• This equipment is not intended for use during patient transport outside the healthcare facility.

• This equipment should not be used adjacent to or stacked with other equipment.

• It may be unsafe to:

• Use accessories, detachable parts, and materials not described in the instructions for use.

• Interconnect this equipment with other equipment not described in the instructions for use.

• Disassemble, repair, or modify the equipment.

• These materials that contact with the patient’s skin contain medical silicone and ABS plastic enclosure and all pass the ISO10993 5 Tests for invitro cytotoxicity and ISO10993 10 Tests for irritation and delayed type hypersensitivity.

• When the signal is not stable, the reading may inaccurate. Please do not reference.

MAINTENANCE & STORAGE

• Replace the batteries in a timely manner when the battery

indicator is blinking.

• Clean the surface of the ngertip oximeter before it is used in

diagnosis for patients.

• Remove the batteries if the oximeter is not used for a long time.

• It is best to store the product in -13°~158°F (-25°~70°C) and ≤

93% humidity.

• Keep in a dry place. Extreme moisture may aect oximeter

lifetime and may cause damage.

• Dispose of the batteries properly. Follow any applicable local

battery disposal laws.

Cleaning the ngertip pulse oximeter

• Disinfection may cause damage to the equipment and is therefore not recommended for this pulse oximeter. If you do need to disinfect the oximeter, clean it before disinfection.

CAUTION: Never use EtO or Formaldehyde for disinfection.

• Use medical alcohol to clean the silicone touching the nger inside the oximeter with a soft cloth dampened with 70% isopropyl alcohol.

Note: Do not immerse the oximeter in disinfectant or sterilizer.

• Clean the nger being tested with alcohol before and after each test. The recommended disinfectants include: ethanol 70%, isopropanol 70%, and glutaraldehyde type 2% liquid disinfectants.

• Do not pour or spray liquids onto the oximeter, and do not allow any liquid to enter any openings in the device. Allow the oximeter to dry thoroughly before reuse.

• The pulse oximeter requires no routine calibration or maintenance other than replacement of batteries.

The use life of the device is ve years when it is used for 15 measurements every day and 10 minutes per one measurement. Stop using and contact customer service if any of the following occurs:

• "Err7" (indicating the emission LED or reception diode is damaged) is displayed on screen.

• The oximeter won't turn on after replacing the batteries.

• There is a crack on the oximeter or damage on the display resulting in reading that cannot be identied, the spring is invalid, or the key is unresponsive or unavailable.

SPECIFICATIONS

Dimensions (H × W × D): 1.3 × 1.5 × 2.3 in. (33 × 37 × 58 mm) Weight (with batteries): 0.1 lbs. (50 g) Display Type: OLED display SpO2:

• Display range: 0%~100%

• Measurement range: 70%~100%

• Accuracy: 70%~100% ±2 %; 0%~69% no denition

• Resolution: 1%

Note:

A functional tester can't be used to assess the accuracy of a pulse oximeter monitor or sensor. Clinical testing is used to establish the

accuracy. The measured arterial hemoglobin saturation value

SpO

(SpO2) of the sensors is compared to arterial hemoglobin oxygen (SaO2) value, determined from blood samples with a laboratory CO-oximeter. The accuracy of the sensors in comparison to the CO-oximeter samples measured over the SpO2 range of 70~100%. Accuracy data is calculated using the root-mean-squared (Arms value) for all subjects, per ISO 9919:2005, Medical Electrical Equipment - Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use. A functional tester is used to measure how accurately Fingertip Pulse Oximeter is reproducing the specied calibration curve and the PR accuracy. The model of functional tester is Index2 FLUKE simulator and the version is 2.1.3.

Pulse Rate

• Display range: 0 bpm~250 bpm

• Measure range: 30 bpm~250 bpm

• Accuracy: 30 bpm~99bpm, ±2 bpm;

100 bpm ~250 bpm, ±2%

• Resolution: 1bpm

Probe LED

• RED: Wavelength - 660±3nm

Radiant power - 3.2mw

• IR: Wavelength - 905±10nm

Radiant power - 2.4mw Note: The information about wavelength range can be especially

useful to clinicians.

Power Requirements

• Two AAA alkaline batteries

• Power consumption: Less than 40 mA

Environment Requirements

• Operation Temperature: 41˚F~104˚F (5˚C~40˚C)

• Storage Temperature: -13˚F~+158˚F (-25˚C~+70˚C)

• Ambient Humidity: 15%~93% no condensation in operation; ≤93% no condensation in

storage/transport

• Atmosphere pressure: 70 kPa~106 kPa

Inaccurate measurements may be caused by:

• Signicant levels of dysfunctional hemoglobin (such as carbonyl hemoglobin or methemoglobin).

• Intravascular dyes such as indocyanine green or methylene blue.

• High ambient light. Shield the sensor area if necessary.

• Excessive patient movement.

• High frequency electrosurgical interference and debrillators.

• Venous pulsations.

• Placement of a sensor on an extremity with a blood pressure cu, arterial catheter, or intravascular line.

• The patient has hypotension, severe vasoconstriction, severe anemia, or hypothermia.

• The patient is in cardiac arrest or is in shock.

• Fingernail polish or false ngernails.

• Weak pulse quality (low perfusion).

• Low hemoglobin.

TROUBLESHOOTING

PROBLEM

Oxygen saturation (SpO2) or pulse rate (PR) is not normal.

Oxygen saturation (SpO2) or pulse rate (PR) is not stable.

The oximeter cannot be turned on.

The screen suddenly turned o.

“Err7” is displayed on screen.

POSSIBLE REASONS SOLUTION

• Finger is not inserted correctly.

• Patient’s SpO2 value is too low to be measured.

• Finger might not be inserted deep enough.

• Excessive patient movement.

• The battery power is low.

• Batteries are installed incorrectly.

• The oximeter is damaged.

• The oximeter automatically turns o when no signal is detected for longer than eight seconds.

• The battery power is low.

The emission LED or reception diode is damaged.

• Remove your finger and reinsert it. Try a few times to make sure your finger is correctly positioned.

• Exposed to direct sunlight

• Insert a different finger into the oximeter.

• If your numbers are not normal, see your doctor for an exact diagnosis.

• Remove your finger and reinsert it. Try a few times to make sure your finger is correctly positioned.

• Make sure that your nger, hand, and body are still while taking a reading.

• Replace batteries

• Make sure that the batteries are positioned correctly.

• Contact Customer Service.

• This is normal behavior.

• Replace the batteries.

Contact Customer Service.

SYMBOL DEFINITIONS

SYMBOL

DEFINITION

Type BF applied part.

Protected against dripping water

Pulse rate (BPM)

No SpO2 Alarm

Storage temperature and relative humidity

Date of Manufacture

Conformity to WEEE Directive

SYMBOL

DEFINITION

Attention

Oxygen saturation

Low power indication

Serial No

Follow instruction for use

Manufacturer’s information

ONEYEAR LIMITED WARRANTY

Visit www.insigniaproducts.com for details.

CONTACT INSIGNIA:

1-877-467-4289 (U.S. and Canada) 1-800-926-3000 (Mexico) www.insigniaproducts.com

V3 English 21-0155