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GE MAC 600


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GE Healthcare
MAC® 600
Resting ECG
Technical Specifications
Instrument Type
Microprocessor augmented automatic electrocardiograph; 10-leadwire, 12-lead simultaneous acquisition with programmable
lead configuration.
Processing
ECG interpretation: Marquette® 12SL™ ECG Analysis Program for Adults and Pediatrics
Computerized measurements: 12-lead analysis
ECG analysis frequency: 500 samples/second (sps)
Digital sampling rate: 2,000 samples/second/channel
ECG on-screen preview: On-screen preview of acquired 10-second ECG waveform and optional 12SL measurement and
interpretation
Acquisition mode: Pre-acquisition or post-acquisition, provide 10 seconds of instantaneous ECG acquisition
Dynamic range: AC Differential ± 5mV, DC offset ±300 mV
Resolution: 4.88 μV/LSB @ 500 sps
Frequency response: –3 dB @ 0.01 to 150 Hz
Low cut-off frequency: 0.01 Hz, 0.02 Hz, 0.16 Hz or 0.32 Hz (-3 dB limits)
High cut-off frequency: Configurable at 20 Hz, 40 Hz, 100 Hz or 150 Hz
High cut-off frequency: Configurable at 20 Hz, 40 Hz, 100 Hz or 150 Hz
Adaptive AC filter: 47 Hz to 53 Hz when set to 50Hz, 57 Hz to 63 Hz when set to 60 Hz
Common mode rejection: >100 dB (with AC filter switched on)
Input impedance: >10MΩ @ 10 Hz, defibrillator protected
Patient leakage: <10 μA
Special acquisition functions: Disconnected lead detection except RL, excessive AC noise, baseline wander
and muscle tremor messages
Heart rate meter: 30 to 300 BPM ±10% or ±5 BPM, whichever is greater. Heart rates outside this range will not be
displayed
Start-up time: Less than 7 seconds
Patient Information
Supported patient information: Patient ID, secondary ID, age, date of birth, gender.
Alphanumeric entry in T9 type for patient ID and secondary ID.
Display
Display type: 4.3 inch (110 mm) diagonal, TFT LCD with LED graphics backlit (color optional)
Display resolution: 480 X 272 pixels with scrolling waveform
Display data: Heart rate, patient ID, clock, battery power indicator, waveforms, lead labels, speed, gain and
filter settings, warning messages, information messages, prompts. 12-leads standard display.
Writer
Writer technology: Thermal dot array
Writer speed: 5, 12.5, 25, & 50 mm/s
Number of traces: 3 leads + 1 rhythm or 3 leads; user selectable
Writer sensitivity/gain: 2.5, 5, 10, 20, 10/5 (split calibration) mm/mV
Writer speed accuracy: ±5%
Writer amplitude accuracy: ±5%
Writer resolution: Horizontal 40 dots/mm @ 25 mm/s, 8 dots/mm vertical
Paper type: Thermal. Z-fold perforated, 80 mm width, 280 sheets/pack. Roll paper 15.7 m.
Keyboard
Type: Type Membrane keyboard with tactile feedback
Software Standard
Resting ECG mode: Records and prints 12-lead resting ECGs with 10-second duration as a standard feature
Hookup Advisor™: Provides visual indication of signal quality
Multi-language support: Supports 16 languages
Software Options
Measurement: Supports measurement with Marquette 12SL ECG Analysis Program
Measurement and
interpretation: Supports measurement and interpretation with Marquette 12SL ECG Analysis Program
Color: Color display
External storage: 200 ECGs in external memory (SD card)
Transmission: ECG data transmission via serial cable
XML format: ECG storage in XML format
PDF format:1 ECG storage in PDF format
Communication (optional)
MUSE® Cardiology Information System Compatible
Serial cable: ECG transmission to MUSE Cardiology Information System
Serial cable: ECG transmission in XML format
SD card interface: Compatible with MUSE v7
CardioSoft™ Interface
SD card interface: Compatible with Cardiosoft V6.51
Storage (optional)
ECG storage format:
GE storage format for MUSE and CardioSoft.
XML storage format.
PDF storage format.
PDF file name format: User-configurable file name, which includes patient ID, secondary ID, date of birth,
ECG recording date and time
Report Formats
Thermal printer report formats
4 by 2.5s
4 by 2.5s + 1 rhythm lead
4 by 3s
4 by 10s
Autorhythm (10-second ECG data for 3 leads)
Printing of 4 by 10s or Autorhythm for abnormal ECG
Continuous 3-channel rhythm
PDF report format
(A4 format):
4 by 2.5s
4 by 2.5s + 1 rhythm lead
2 by 5s
2 by 5s + 1 rhythm lead
2 by 5s @ 50mm/s
4 by 10s
Autorhythm (12-lead)
Accessories
IEC/AHA leadwire and electrode adaptor sets (user-selectable)
10-lead patient cable (user-selectable replaceable leads or fixed leads cables)
Electrodes (disposable or reusable, user-selectable)
Country-specific power cords
Z-fold and Roll paper
Electrode cream 250 ml/tube
Electrical
Power supply: External AC/DC adaptor or battery operation
External Adaptor Specifications
Input voltage: 100 to 240 VAC ±10%
Input current: Maximum 0.6A @ 90 VAC, 0.3A @ 240 VAC
Input frequency: 50 to 60 Hz ± 3Hz
Output voltage: 12V ± 5%
Battery Specifications
Battery type: Replaceable and rechargeable, Lithium Ion
Battery capacity:
7.2V typical, 2.25 AH ±10%
360 minutes of continuous operation without recording or
250 ECGs in 2.5 X 4 format at 25 mm/S and 10 mm/mV or
100 minutes continuous rhythm print at 25 mm/S and 10 mm/mV.
Battery charge time: Approximately 3 hours from total discharge (with display off)
Physical Specification
Height: 81 mm
Width: 263 mm
Depth: 208 mm
Weight: 1.2 Kg including battery, without paper
1ECG storage in PDF format is not supported in Russian language.
Environmental Specification
Temperature
Operating 5°C to 40°C
Transport/storage: -15°C to 50°C
Humidity
Operating: 25% to 95% RH non-condensing
Transport/storage: 25% to 95% RH non-condensing
Pressure
Operating: 700 to 1060 hPA
Transport/storage: 500 to 1060 hPA
Certification
Class II, type CF defibrillator proof
UL 60601-1 Medical Electrical Equipment, part 1: General Requirements for Safety
CAN/CSA C22.2 No. 601.1 General Requirements for Safety
CE marking for Council Directive 93/42/EEC concerning medical devices
IEC 60601-1 General Requirements for Safety
IEC 60601-1-1 General Requirements for Safety Medical Electrical systems
IEC 60601-2-25 Particular Requirements for the Safety of Electrocardiographs
IEC 60601-2-51 Particular Requirements for Safety, including essential performance, of recording and analyzing single channel
and multi channel electrocardiographs
IEC 60601-1-2 General Requirements for Safety Electromagnetic Compatibility
IEC 60601-1-4 General Requirements for Safety – Programmable electrical medical systems
IEC 60601-1-6 General Requirements for basic safety and essential performance – Collateral Standard: Usability-Edition 2.0
Meets applicable AAMI EC-11 requirements and AAMI EC 13 (Clause 4.2.7 only)
GE imagination at work
GE Healthcare
Munzinger Straße 5
79111 Freiburg, Germany
Tel. +49 761 4543 0 • Fax +49 761 4543 233
www.gehealthcare.com
EMEA 2050698-002/0210
©2010 General Electric Company – All rights reserved.
General Electric Company reserves the right to make changes
in specifications and features shown herein, or discontinue the
product described at any time without notice or obligation.
Contact your GE Representative for the most current information.
GE and GE Monogram are trademarks of General Electric
Company.
MAC and Marquette and MUSE are registered trademarks of
General Electric Company.
12SL, CardioSoft and HookUp Advisor are trademarks of
General Electric Company.
GE Healthcare, a division of General Electric Company

  
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