Masimo Radical Signal Extraction Betreibershandbuch PDF herunterladen (Seite 6)

Radical-7 Signal Extraction Pulse CO-Oximeter Operator’s Manual

SAFETY INFORMATION, WARNINGS, CAUTIONS AND NOTES (CONTINUED)

■ Severe anemia

■ Low arterial perfusion

■ Motion artifact

■ Inaccurate SpHb and SpOC readings can be caused by:

■ Intravascular dyes such as indocyanine green or methylene blue

■ Externally applied coloring (such as nail polish)

■ Elevated levels of Bilirubin

■ Low arterial perfusion

■ Motion artifact

■ Low arterial oxygen saturation levels

■ Hemoglobin synthesis disorders

■ Hemoglobinopathy

■ Peripheral vascular disease

■ EMI radiation interference

■ Inaccurate SpCO and SpMet readings can be caused by:

■ Elevated levels of Bilirubin

■ Motion artifact

■ Low arterial oxygen saturation levels

■ Do not place the Radical-7 against a surface. This can cause a system or battery (non-

clinical) alarm to be muffled.

■ For home use, ensure that the Radical-7's alarm can be heard from other rooms in the

house, especially when noisy appliances such as vacuum cleaners, dishwashers, clothes

dryers, televisions, or radios are operating.

■ Additional information speciﬁ c to Masimo sensors, including information about parameter/

measurement performance during motion and low perfusion, may be found in the sensor's

Directions for Use (DFU).

■

If the

Radical-7

fails any part of the setup procedures or leakage tests, remove the

Radical-7

from operation until qualiﬁ ed service personnel have corrected the situation.

■

Do not incinerate battery.

■

Disposal of product - Comply with local laws in the disposal of the instrument and/or its accessories.

■ To protect against injury from electric shock, follow the directions below:

■ Do not place the instrument near water.

■ Avoid placing the instrument on surfaces with visible liquid spills.

■ Do not soak or immerse the instrument in liquids.

■ Always turn off and disconnect the power cord from the AC power supply before cleaning

the instrument.

■ Use cleaning solutions sparingly.

■ This equipment has been tested and found to comply with the limits for medical instruments

to the EN 60601-1-2: 2002, Medical Instrument Directive 93/42/EEC. These limits are

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