Patient Safety; Warnings - Novametrix Medical Systems MARS PO2 TECH 2001 Service Manual

Section 1
The SpO
current flowing from the instrument to ground is limited to less than 25 mA at 120 VAC, 60 Hz.
Patient isolation is greater than 10 MΩ, 4000 VAC rms at 60 Hz. The Model 2001 is Year 2000
compliant.
For maximum patient and operator safety, the following are recommended:
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Warnings

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Rev. 01
input for the Model 2001 Pulse Oximeter is electrically isolated. Patient leakage
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Failure of Operation: If the monitor fails to respond as described, do not use it until the
situation has been corrected by qualified personnel.
Keep Model 2001 and its accessories clean.
Do not operate Model 2001 when it is wet due to spills or condensation.
Do not operate Model 2001 if it appears to have been dropped or damaged.
Connect the line cord only to a grounded hospital-grade outlet. Model 2001 should be
connected to the same electrical circuit as other equipment in use on the patient. Outlets
on the same circuit can be identified by the hospital's engineering department.
Care should be exercised to assure continued peripheral perfusion distal to the SpO
sensor site after application.
Components of this product and its associated accessories which may have patient
contact are free of latex.
The Model 2001 contains no user serviceable parts. Refer servicing to qualified service
personnel.
Indicates a potentially harmful condition that can lead to personal injury
Explosion Hazard: Do NOT use Model 2001 in the presence of flammable anesthetics.
Use of this instrument in such an environment may present an explosion hazard.
Electrical Shock Hazard: Always turn Model 2001 off and remove line cord before
cleaning it. Do NOT use a damaged sensor or one with exposed electrical contacts. Refer
servicing to qualified service personnel.
Do not operate Model 2001 when it is wet due to spills or condensation.
Do not operate Model 2001 if it appears to have been dropped or damaged.
Patient Safety: Extreme care should be exercised with neonates to assure continued
circulation distal to the sensor site after application.
Failure of Operation: If the monitor fails to respond as described, do not use it until the
situation has been corrected by qualified personnel.
Patient Safety: Care should be exercised to assure continued peripheral perfusion distal
to the SpO sensor site after application.
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WARNING
Model 2001 Service Manual

Patient Safety

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