Product Manual

2
Indications for Use
This equipment complies with International IEC 60601-1-2:2007 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.
Only use Nonin-branded sensors with a length of 1 meter or less. Accuracy may degrade if sensor cable is over
1 meter in length. Using the sensor cable adapter does not affect accuracy.
Cautions
If this device fails to respond as described, refer to “Troubleshooting” or discontinue use until the situation has
been corrected. Contact Nonin Technical Service.
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.
When setting the clock in Programmed Mode using nVISION software, verify all set times and dates are valid.
Do not place the WristOx
2
, Model 3150, in liquid or clean it with agents containing ammonium chloride or
isopropyl alcohol. Refer to the “Care and Maintenance” section of this operator’s manual.
Use a detergent that is safe for skin and washable surfaces. Most detergents can be high sudsing, so use
sparingly. Wipe with a damp, detergent free cloth to remove residue.
After cleaning the single-patient use wristband, it should only be applied to the same patient; do not apply it to a
different patient.
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.
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:
Do not perform any testing or maintenance on this device while it is being used to monitor a patient.
This device is a precision electronic instrument and must be repaired by qualified technical professionals. Field
repair of this device is not possible. Except to replace batteries, do not attempt to open the case or repair the
electronics. Opening the case may damage the device and void the warranty.
Warnings (Continued)
- excessive ambient light
- excessive motion
- electrosurgical interference
- blood flow restrictors (arterial
catheters, blood pressure cuffs,
infusion lines, etc.)
- moisture in the sensor
- improperly applied sensor
- incorrect sensor type
- poor pulse quality
- venous pulsations
- anemia or low hemoglobin
concentrations
- cardiogreen and other
intravascular dyes
- carboxyhemoglobin
- methemoglobin
- dysfunctional hemoglobin
- artificial nails or fingernail
polish