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It's not applicable to overshoot pacemaker pulse.
6. Pacemaker pulse rejection for the ECG signal: the minimum input slew-rate is 2V/s RTI (it varies on different
filter modes, ).
7. This device (including the accessories, such as Cuff, SpO
have special protection against defibrillator.
8. When the device is used together with electro-surgical unit, the ECG signal display could return to its previous
normal state within 10s after exposure to the field produced by the electro-surgical unit without loss of any
stored data.
9. When the power line interference (50Hz/60Hz) is very high, the pacemaker pulse might be falsely detected.
10. Pacemaker pulse rejection warning label: see Section 3.4.3 & Section 8.1.
11. Auxiliary output: Not provided
12. Remote technology: Not provided
6.10.2 Additional description for SpO
1. The device is calibrated in the factory before sale, so there is no need to calibrate it during its life cycle. Any
SpO
simulators should not be used to validate the accuracy of the oximeter, they can only be used as functional
2
testers to verify its precision. The SpO
conducted by inducing hypoxia on healthy, non-smoking, light-to-dark skinned subjects in an independent
research laboratory.
2. If it is necessary to verify the precision of the oximeter routinely, the user can do the verification by means of
SpO
simulator, or it can be done by the local third party test house. Please note that the specific calibration curve
2
(so called R-curve) should be selected when use of SpO
Fluke Biomedical Corporation, please set "Make" to "DownLoadMake: KRK", then the user can use this
particular R-curve to test the oximeter. If the SpO
manufacturer for helping to download the given R-curve into the SpO
3. The average data update period: ≤10s
6.10.3 Additional description for NIBP measurement
The blood pressure measured by this device is essentially identical to that measured by auscultatory method.
6.10.4 Additional description for temperature measurement
This monitor adopts the thermistor-type probe to make temperature measurement. The constant micro direct current
of the temperature probe is 32µA, and the dissipation power (I2R) is related to the probe type. If you choose KRK
temperature probe, then the Static Power is less than 17 µW in the range from 15℃ to 55℃; if you choose YSI
temperature probe, then the Static Power is less than 3 µW in the range from 25℃ to 45℃. The produced
self-heating will not result in the measurement deviation exceeds the declared specification.
6.10.5 Additional description for alarm system
1. Alarm indication: audial and visual alarm signal
2. Audial alarm:
²
High priority alarm: one group pulse string including 10 pulse; x, x, 2x + td, x, 1s, x, x, 2x + td, x, and
x=100ms, the pulse duration is160ms, pulse frequency is 400Hz, the pulse string interval is 3s.
²
Medium priority alarm: one group pulse string including 3 pulse, the pulse string interval is y, y, and y=200ms,
the pulse duration is200ms, pulse frequency is 500Hz, the pulse string interval is 5s.
²
Low priority alarm: the unrepeatable single pulse, frequency is 500Hz, and pulse duration is 200mx.
3. Visual alarm: The visual alarm includes the LED indicator located on the upper front panel of the Monitor, the
numeric readings flashing, and the alarm message displayed on the bottom of the LCD screen. Alarm indicator
frequency and color see below:
Alarm LED indicator: High-priority: red light flashing with 2Hz frequency and 50% duty ratio
Low priority: Yellow light flashing with 2Hz frequency and 50% duty ratio
Medium priority: Yellow light on
No alarm: Green light on
probe and the internal ECG module) is designed to
2
monitoring
2
accuracy claimed in this manual is supported by the clinical study
2
simulator, e.g. for Index 2 series SpO2 simulator from
2
simulator does not contain "KRK" R-curve, please ask the
2
48
simulator.
2
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