F&P Airvo 3 Bedienungsanleitung Seite 49

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Pulse oximetry
Specifications are tabulated for the Airvo 3 and all compatible sensors unless otherwise stated.
Nonin:
Data update period
Measurement wavelengths and Output Power* Red: 660 nanometers @ 0.8 mW max. avg.
SpO Accuracy (A )
**
2 rms
No Motion
Reusable
8000AX Series:
800XJ Series:
8000SX Series:
8000R:
8000Q2:
Disposable
6000CX Series:
7000X Series:
Motion
Reusable
8000AX Series:
800XJ Series:
8000SX Series:
Low Perfusion****
Pulse Rate Accuracy
No Motion (18–300 BPM)
Reusable
8000AX Series:
800XJ Series:
8000SX Series:
8000R:
8000Q2:
Disposable
6000CX Series:
7000X Series:
Motion (40–240 BPM)
Reusable
8000AX Series:
800XJ Series:
8000SX Series:
Low Perfusion (40–240 BPM)****
* This information is especially useful for clinicians performing photodynamic therapy.
± 1 A
** represents approximately 68% of measurements.
rms
*** Includes Infant patients
**** Does not apply to those sensors listed as N/A under the neonate column, 8000R and 8000Q2
Notes:
• SpO accuracy testing is conducted during induced hypoxia studies on healthy, non-smoking, light-to-dark-skinned subjects during motion and
2
no-motion conditions in an independent research laboratory. The measured arterial hemoglobin saturation value (SpO
compared to arterial hemoglobin oxygen (SaO
sensors in comparison to the co-oximeter samples measured over the SpO
squared (Arms value) for all subjects, per ISO 80601-2-61 formerly ISO 9919, Standard Specification for Pulse Oximeters for Accuracy.
• Pulse rate motion testing measures pulse rate accuracy with motion artifact simulation introduced by a pulse oximeter tester. This test
determines whether the oximeter meets the criteria of ISO 80601-2-61, formerly ISO 9919, for pulse rate during simulated movement, tremor, and
spike motions.
• Low perfusion testing uses an SpO
module must maintain accuracy in accordance with ISO 80601-2-61, formerly ISO 9919, pulse rate and SpO
amplitude (0.3% modulation).
<30 sec
Infrared: 910 nanometers @ 1.2 mW max avg. (using Nonin Purelight® sensor)
70 to 100%
Adults/Pediatrics***
± 2 digits
± 3 digits
± 2 digits
± 3 digits
± 3 digits
± 2 digits
± 2 digits
± 2 digits
± 3 digits
± 3 digits
± 2 digits
Adults/Pediatrics***
± 3 digits
± 3 digits
± 3 digits
± 3 digits
± 3 digits
± 3 digits
± 3 digits
± 5 digits
± 5 digits
± 5 digits
± 3 digits
) value, determined from blood samples with a laboratory co-oximeter. The accuracy of the
2
Simulator to provide a simulated pulse rate, with adjustable amplitude settings at various SpO
2
Neonates
N/A
N/A
N/A
N/A
N/A
± 3 digits
± 3 digits
N/A
N/A
N/A
± 3 digits
Neonates
N/A
N/A
N/A
N/A
N/A
± 3 digits
± 3 digits
N/A
N/A
N/A
± 3 digits
range of 70–100%. Accuracy data is calculated using the root-mean-
2
2
) of the sensors is
2
levels. The
2
at the lowest obtainable pulse