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severely degraded (this will happen over time and use), but DO NOT use the AC/DC adapter if batteries
other than rechargeable NiMH batteries are installed in the unit.
Do not mix rechargeable and non-rechargeable batteries. When replacing batteries, replace all
batteries with the same type. Do not mix old and new batteries.
When connecting this monitor to any equipment or accessories, verify proper operation before
clinical use. Accessory equipment connected to the petMAP's USB port should be certified according to
the respective IEC standards, i.e. IEC 60950 for data processing equipment or IEC 60601-1 for electro
medical equipment. All combinations of equipment should be in compliance with IEC 60601-1-1 systems
requirements. Anyone connecting additional equipment to the USB signal input port /signal output port
configures a medical system, and therefore, is responsible that the system complies with the
requirements of the system standard IEC 60601-1-1
.
The petMAP+II is intended for VETERINARY USE ONLY. Do not use on a human patient.
Do not apply the blood pressure cuff on an extremity being used for an IV solution.
Do not place the SpO2 sensor distal to the blood pressure cuff.
Using a damaged SpO2 sensor may cause inaccurate readings. If a sensor appears damaged, do
not use it. Contact CardioCommand, Inc. to purchase a replacement sensor.
Use only SpO2 sensors supplied with, or specifically intended for use with, this device.
Under certain clinical conditions the pulse oximeter may display “?” if unable to display SpO2
and/or pulse rate values. Under these conditions, pulse oximeters may also display erroneous values.
These conditions include, but are not limited to: patient motion, low perfusion, cardiac arrhythmias,
high or low pulse rates, electrical interference from electro cautery or other ESU devices, or a
combination of the above conditions. It is the responsibility of the clinician to recognize the effects of
these conditions on pulse oximeter readings and proceed accordingly.
Do not immerse the device or AC/DC adapter in water or any liquid. If the unit is accidentally
wetted, it should be thoroughly dried before use.
To ensure that the unit remains in calibration, verify calibration on a yearly basis or at any time
there is user suspicion that proper calibration may have been lost.
If the petMAP+II has been dropped or damaged in any way, it should be checked by qualified
service personnel to ensure proper operation prior to use.
Use of accessories other than those specified by Ramsey Medical may result in increased
electro-magnetic (EM) emissions or decreased EM immunity of the device.
Follow local governing ordinances and recycling instructions regarding disposal and recycling of
device components and packaging.
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