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Philips FM20/30 Instructions For Use Manual Page 274

Release j.3 with software revision j.3x.xx patient monitoring.
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28 Specifications and Standards Compliance
Performance Specifications
Auto Mode Repetition Times
Venipuncture Mode Inflation
Inflation Pressure
Automatic deflation after
*1: Clinical investigation with the auscultatory reference method
The 5th Korotkoff sound (K5) was used to determine the diastolic reference pressures.
The approximation MAP = (2*DIA + SYS) / 3 was used to calculate reference MAP (mean
arterial pressure) values from the systolic and diastolic reference pressures.
The NBP measurement is suitable for use with pregnant (including pre-eclamptic) patients.
Alarm Specifications
Overpressure Settings
> 300 mmHg (40 kPa) > 2 sec
Complies with ISO 80601-2-61:2011 / EN 80601-2-61:2011.
Measurement Validation: The SpO
blood sample reference measured with a CO-oximeter. Pulse oximeter measurements are statistically
distributed, only about two-thirds of the measurements can be expected to fall within the specified
accuracy compared to CO-oximeter measurements.
Display Update Period: Typical: 2 seconds, maximum: 30 seconds. Maximum with noninvasive blood
pressure INOP suppression on: 60 seconds.
1, 2, 2.5, 3, 5, 10, 15, 20, 30, 45, 60, or 120 minutes
20—120 mmHg (3—16 kPa)
170 seconds
Adult: 30—
10—30 mmHg: 2 mmHg (0.5 kPa)
270 mmHg (4—
>30 mmHg: 5 mmHg (1 kPa)
36 kPa)
Adult: 10—
245 mmHg (1.5—
32 kPa)
Adult: 20—
255 mmHg (2.5—
34 kPa)
accuracy has been validated in human studies against arterial
not user adjustable
Alarm Delay
System alarm delay
(see "Fetal Monitors" on
page 267).


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