Product Specification Εκτύπωση E-mail
Physical
Size 2.75 in high X 8.66 in wide X 10.23 in deep
(70mm high X 220 mm wide X 260 mm deep)
Weight Approximately 4.84 lbs (2.2 kg)
with battery pack installed
Environmental
Operating Conditions Temperature 32ΛXF to 110ΛX;F (0ΛXC to 43 ΛXC)
Humidity 5 % to 95 % (non-condensing)
Storage Conditions Temperature 32ΛXF to 110 ˚F (0 ΛXC to 43 ΛXC)
Humidity 5 % to 95 % (non-condensing)
Shock/Drop/Abuse Tolerance Meets IEC 60601-1 clause 21 (Mechanical Strength)
Vibration Meets EN1789 random and swept sine, road ambulance specification in operating and standby states.
Sealing IEC 60529: IP54
ESD Meets IEC 61000-4-2:2001
EMI (Radiated) Meets IEC 60601-1-2 limits, method EN 55011:1998+ A1:1999 +A2:2002, Group 1, Class B
EMI (Immunity) Meets IEC 60601-1-2 limits, method EN 61000-4-3:
2001 Level 3 (10V/m 80MHz to 2500MHz)
Defibrillator
Operating Mode Semi-automated
Waveform e-cube biphasic (Truncated exponential type); impedance compensated
Energy 200 Joules nominal into a 50Ω load
Shock Energy Accuracy Within ±3% (150J into 50Ω)
Charge Control Automatic by Software (Arrhythmia Detection System and Charging Control)
Charge time from “Shock Advised” < 14 seconds, typical
Shock to Shock cycle time < 15 seconds, typical, including analysis
Charge complete indicator * Text prompt (PRESS THE FLASHING ORANGE BUTTON, NOW)
* flashing backlight of SHOCK button
* beep from the beeper
Disarm Once charged, the NF1200 disarms if:
* Patient’s heart rhythm changes to non-shockable rhythm, or
* The SHOCK button is not pressed within 15 seconds after the NF1200 is armed, or
* The ON/OFF button is pressed to turn OFF the NF1200, or
* The defibrillator pads are removed from the patient or the pads connector is disconnected from the NF1200
Defibrillator, continued
Shock Delivery Shock is delivered if the SHOCK button is pressed while the NF1200 is armed.
Shock Delivery Vector Via adult defibrillator pads in the anterior-anterior (Lead II) position or via Reduced-energy pediatric pads in the anterior-posterior position.
Patient Isolation Type BF
ECG Acquisition
Acquired ECG Lead Lead II
Frequency Response 1 Hz to 30 Hz EMS Mode
0.3 Hz to 40 Hz Monitoring Mode
ECG Analysis System
Function Determines the impedance of the patient and evaluates the ECG of the patient to determine whether it is shockable or non shockable
Impedance Range 25Ω to 175Ω
Shockable Rhythms Ventricular Fibrillation or Fast Ventricular Tachycardia
Non Shockable Rhythms ECG rhythms other than Ventricular Fibrillation or Fast Ventricular Tachycardia
Sensitivity & Specificity: Meets AAMI DF39 guidelines
Controls, Indicators, and Prompts
Controls Power On/Off Button,
i-Button,
Shock Button
Indicators State LED, Graphical Rescue Guide LED
Audio Speaker Provides voice prompts
Beeper Provides various audible indications
Low Battery Detection Automatic during daily testing and Power ON and runtime testing
Low Battery Indicator State LED and Voice Prompt
Prompts Voice prompts guide the user throughout a rescue operation
Self-Tests
Automatic * Power On Self-Test / Run Time Self-Test
* daily / weekly/ monthly
User Initiated Battery Insertion Test
Battery Pack
Battery Type 12 Volt DC, 4.2 Ah, lithium manganese dioxide, disposable long-life primary cell.
Capacity Minimum 200 shocks or 4 hours of operating time.
Temperature Range -40 Β°F to 140 Β°F (-40 Β°C to 60 Β°C)
Defibrillator Pads (CUA0512F)
Type self-adhesive, disposable, non-polarized defibrillation pads
Adult Pads Defibrillation pads for patients 8 years of age and older or 55 lbs. (25 kg) and over.
Surface Area Adult : 110cm2 each
Cable Length 1.5m
Data Recording and Transmission
Infrared Wireless transmission of event data to PC through IrDA port.
Data Stored First 40 minutes of ECG and the entire incident’s events and analysis decisions.
 
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