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Section 9- Technical Specifications
CLASSIFICATION
Protection against electroshock
Class I, Type CF , defibrillation-proof applied part
Mode of operation
Continues operation equipment
Harmful Liquid Proof Degree
Ordinary equipment, (without Liquid Proof)
Method of sterilization and disinfection
Refer to chapter 10 for detail.
Safety of anesthetic mixture
Not suitable for use in the presence of a flammable anaesthetic
mixture with air or with oxygen or nitrous oxide.
DISPLAY
Display
TFT COLOR, 4.3’’
Resolution
480
272
Waveforms
12 Lead ECG/Rhythm Lead
Numeric Parameters
HR
Operation Method
Membrane Keys and Touch
Displayed data
Waveforms, Patient Information (Name and ID), Data &
Time, Recording Speed, Sensitivity, Operation Mode, Filter,
HR Value, Message
ECG
Input Channel
Simultaneous acquisition of all 12 leads/ Rhythm Lead
Standard leads acquired
I, II, III, aVR, aVF, aVL, V1, V2, V3, V4, V5, V6
Sensitivity Selection
2.5, 5, 10, 20 mm/mV
Filters
Drift: on or off
HUM: 50 or 60 HZ, off
Low pass: 25, 35, 75, 150 HZ
EMG: On or Off
Calibration
1 mV
Dynamic Range
±5 mV
Leakage Current
< 10 μA
CMRR
> 98 dB
Time Constant
3.2 sec.
Frequency Response
0.05~150 Hz
Pace
Detection & Rejection: 0.1~2 ms, ±2~±250 mV
Protection
Defibrillator
Standards
IEC 60601-2-25