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User’s
Manual for OMNI Express Patient Monitor
94
037.007.0001 Rev.2
SPECIFICATIONS
SAFETY
Meet the requirement of EN60601 series, CE marking according to MDD93/42/EEC
Equipment not suitable for use in the presence of a flammable anesthetic mixture with air
or with oxygen or nitrous oxide
Type of Protection:
Class I (on AC power)
Internally powered (on battery power)
Degree of Protection:
Type BF, defibrillation-proof CF - Applied part
Sterilization or Disinfection methods:
70% isopropyl alcohol solution or a nonstaining
disinfectant.
Operation Mode:
Continuous Operation
Protection Against Ingress of Liquid’s:
IPX0
APPLICATION
Neonatal, pediatric and adult patients
Physical Dimensions & Weight
Base Unit:
229×133×210 mm
Weight:
2.5 kgs
PEFORMANCE SPECIFICATIONS
Display:
7.0 Inch (Diagonal) Color TFT
Resolution:
800 × (RGB) × 480
Trace:
2 or 3 waveforms
Waveforms:
ECG(I, II, III, aVR, aVL, aVF, V), PLETH, RESP,
EtCO
2
Indicator:
Alarm indicator
Power indicator
QRS beep and alarm sound
Trend time:
60 hours
ECG
Input:
3 or 5 ECG cable and standard AAMI line for
connection
Standards:
ANSI/AAMI EC13
EN60601-2-27 / IEC60601-2-27
Lead Choice:
3-Lead: I, II, III
5-Lead: I, II, III, aVR, aVL, aVF, V
Gain Choice:
×0.25
,
×0.5
,
×1.0
,
×2.0
ECG Waveforms:
3 channels
CMRR (Common Mode Rejection
Ratio):
≥
89 dB at 50 Hz or 60 Hz
Frequency Characteristic:
0.67
~
40 Hz
(
+3dB attenuation
)
Differential Input Impedance:
>5 MΩ
Sweep Speed:
12.5, 25 and 50 mm/s
HR Display Range:
30
~
300 bpm
Accuracy:
±1bpm or ±1%, whichever is greater
Alarm Limit:
Upper Limit: 80
~
400 bpm
Lower Limit: 20
~
150 bpm
Electrode Offset Potential Tolerance:
± 300 mV
Input Signal Range:
±5 mV ( peak-to-peak value)
Base Line Recovery Time:
<5 s after defibrillation
Bandwidth(-3dB):
Diagnostic Mode: 0.05 Hz
~
130 Hz
Monitor Mode : 0.5 Hz
~
40 Hz
Surgical Mode : 1 Hz
~
20 Hz
Recovery:
<8 s
Pace Pulse Markers:
Pace pulses meeting the following conditions are