LIFEGARD II with ICG & EtCO2 Data Sheet - ANALOGIC - #2

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CO2
Complies with EN 864/1SO 9918
Range: 0to99mmHg(0to13kPa), or 13%CO2
whichever is lower. Flow Rate: 50 ±7.5 ml/min
Warm-up Time: 180 seconds max.; typically 30 seconds Gas Sampling Delay Time: 2.7 seconds Resolution
Numeric: 1.0 mmHg (0.1 kPa)
Wave: 0.1 mmHg (0.01 kPa)
Rise Time: 190 ms for adult mode (measured with sample line for humidified ventilation and airway adapter for adult)
Calibration Interval: 4,000 operating hours
Auto Zero Intervals: < 2% duty cycle. Increases if the temperature changes by 8°C from the previous Auto­Zero interval, or the pressure changes by 45 mmHg.
Leak Tightness: < 40 mbar/min with 30% vacuum
Accuracy
0 - 20 minutes: 0 to 38 mmHg ±4 mmHg; 38 to 99
mmHg ±12% of indicated value
Waveforms
Up to 4 traces (selectable in any combination of 2
ECG, 1CG, etCO2,SpO2 plethysmograph,
or respiration) 1ndicators
Categorized alarms (3 priority levels with different tone pitch)
Visual alarm notification
Heart rate tone
Battery status
External power LED Battery (standard)
1nternal battery: sealed lead-acid
Battery status indicator
Operating Time: 3 hours typ. (fully charged battery) Thermal Printer:
Speeds: 12.5, 25, and 50 mm/sec
Weight: 0.4 kg (0.9 lb.)
PaperWidth:50mm Compliance and Approvals
CE marking: Medical Device Directive, 93/42/EEC Safety Standards: 1EC 60601-1,1EC 60601-1-1,
UL 60601-1, CAN/CSA C22.2 No 601.1 (M90),
EN 60601-1
Water Resistance: 1EC 60529 Classification 1PX1 Mechanical Shock: 1EC 60068-2-27
Environmental Humidity: 1EC 60068-2-78
Environmental Temperature: 1EC 60068-2-1,
1EC 60068-2-2
Electromagnetic Compatibility: 1EC 60601-1-2
UL60601-1, CAN/CSA-22.2 No. 601.1 (M90)
1EC/EN 60601-14
1EC/EN 60601-1-8
1EC/EN 60601-2-27
1EC/EN 60601-2-30
1EC/EN 60601-249
EN 864
EN 865
EN1060-1 EN1060-3
ANS1/AAM1SP10
1SO 9918
Graphical and Tabular Trends
Memory Storage: 72 hours Data Interval: 20 seconds DisplayRange:2hours,72hoursscrollable Tabular Format: One table for all variables;
six fields per row (time and 5 vital signs) Display Interval: Per N1BP measurement or
15 minutes if no N1BP, or during an alarm
condition
A
\ujusiaui trends
e vertical scaling when using graphical
Stored Data: Trend data for HR, SpO2,NlBP, awRR, etCO2 Temp; plus 17 Hemodynamic Values: SV/S1. CO/C1, SVR/SVR1, TFC/TF1,AC1,V1, EV1, PEP,
LVET,ETR,STR,LCW1,H1. Any2parametersmay
be graphically trended
Interfaces
E1A-232 digital output from the serial port for one of the following: nurse call
transferring data to an external computer transferring patient data and waveforms to
L1FEGARD Vue Central System
Physical
Weight: 5.7 kg (125 lb.) excluding
accessories, options, cables Size: 34.3 cm x 25.4 cm x 17.8 cm
(135" x 10.0" x 7.0")
Monitor Environmental
Operating Temperature: 5°C to 45°C (41°F to 113°F) Storage Temperature: - 20°C to 60°C (- 4°F to 140°F) Operating/Storage Humidity: 20% to 90% relative humidity, non-condensing Operatng Altitude: 0to3,048m (0to10,000ft.) Mechanical Shock: 50G
Power
AC 100 to 240 VAC, 50/60 Hz, 1A Monitor Performance
Display TFT color-active matrix
Screen Size: 210.8 mm x 157.5 mm (8.3" x 6.2")
264.2 mm (10.4") diagonally Resolution: 640 x 480 pixel View Angles: 70° left / right, 40° up, 70° down Backlight Life: 25,000 hours
> 20 minutes: 0 to 38 mm
ing ±L I]
mHg 38 to 99
mmHg
±5% of
indicated value +
0.08% for every 1.0 mmHg above 40 mmHg.
Airway Respiration
I (awRR)
Range: 0 to 150 breaths/min
Accuracy: 0 to 41 breaths/min ±1 breaths/min; 41 to 70 breaths/min ±2 breaths/min; 71 to 100 breaths/min ± 3 breaths/min; > 100 breaths/min ±5% of reading
ICG Performance
Measurement principle: TEB
(thoracic electrical bioimpedance) Number of Electrode Pairs: 4
Excitation Current: 1 mARMS ±10%
Excitation Frequency: 76.8 kHz
Basic Thoracic Impedance Range: 0-60Q
Basic Impedance Measurement Bandwidth: 0-10 Hz
Impedance Variation Range: ±1Q
Impedance Noise: < 1 mQ at 50Q basic impedance
Patient Criteria
Adult
Height 4 ft -7 ft 5 in(122 cm -229 cm) Weight: 67 lbs - 360 lbs (30 kg -159 kg) Reduced accuracy of ICG monitoring may result in patients: with minute-ventiliation-rate pacemakers, with chest tubes, with severe arrhythmias, on mechan­ical ventilators, during cardiac surgery, or on intra-aor-tic balloon pump.
Specifications subject to change without notice.
(1) Systolic and Diastolic blood pressure measurements determined with this device are equivalent to those obtained by a trained observer using the cuff/stetho­scope auscultation method, and mean pressure meas­urements determined with this device are equivalent to those obtained by an intra-arterial blood pressure measurement device, within the limits prescribed by the American National Standards Institute and Association for the Advancement of Medical Instrumentation (Electronic or Automated Sphygmomanometers).
LIFEGARD is a registered trademark of Analogic Corporation. Printed in U.S.A.©2005,2007
16-00208-23 Rev 02
Refer to the LIFEGARD II Ordering Guide for additional information.
Analogic Corporation
Life Care Systems Division 8 Centennial Drive Peabody, MA 01960, USA Tel: (978) 326-4000 (800) 599-7769 Fax: (978) 977-6854 www.analogic.com/lifegard

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