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SOMA Technology
Physio Control Lifepak 12

Physio Control Lifepak 12

Brand:   Physio Control
Condition:   SellerRefubrished
The Physio-Control LIFEPAK 12 defibrillator/monitor, when in AED mode, is a semiautomatic defibrillator that uses a patented Shock Advisory System.
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Physio Control Lifepak 12 Features The Physio-Control LIFEPAK 12 defibrillator/monitor, when in AED mode, is a semiautomatic defibrillator that uses a patented Shock Advisory System. This software algorithm analyzes the patient’s electrocardiographic (ECG) rhythm and indicates whether or not it detects a shockable rhythm. The LIFEPAK 12 defibrillator / monitor in AED mode requires operator interaction in order to defibrillate the patient. The LIFEPAK 12 defibrillator/monitor offers the following optional features: Biphasic defibrillation waveform Semi-automatic defibrillation Noninvasive pacemaker Pulse oximeter Interpretive 12-lead ECG Noninvasive blood pressure (NIBP) monitor End-tidal CO2 (EtCO2) monitor Invasive pressure (IP) monitor Vital sign (VS) and ST monitoring Fax transmission Paddle accessories Electroluminescent (EL) display (The optimal viewability of an EL display is compromised in direct sunlight.) Physio Control Lifepak 12 Specifications Physical Weight Basic defibrillator/monitor with QUIK-COMBO cable: 6.6 kg (14.5 lbs) (unit and QUIK-COMBO cable only – no batteries) Fully featured defibrillator/monitor with QUIK-COMBO cable: 8.0 kg (17.6 lbs) (unit and QUIK-COMBO cable only – no batteries) FASTPAK battery: 0.64 kg (1.4 lbs) FASTPAK 2 battery: 0.64 kg (1.4 lbs) LIFEPAK NiCd battery: 0.8 kg (1.7 lbs) LIFEPAK SLA battery: 1.27 kg (2.8 lbs) Height: 31.7 cm (12.5 in) Width: 38.9 cm (15.3 in) Depth: 21.7 cm (8.5 in) Display Size 140.8 mm (5.5 in) wide x 105.6 mm (4.2 in) high for LCD, or 165.1 mm (6.5 in) wide x 123.8 mm (4.9 in) high for EL display Display Type 640 dot x 480 dot black and white LCD or amber and black EL display User selectable display contrast Displays a minimum of 4 seconds of ECG and alphanumerics for values, device instructions, or prompts. Option to display one or two additional waveforms Waveform display sweep speed: 25 mm/sec for ECG, SpO2, IP, and 12.5 mm/sec for CO2 Communications The device is capable of transferring data records by PC Card internal modem, external EIA/TIA modem, cellular modem, or serial connection. Supports EIA/TIA-602 compatible modems using Xon/Xoff or RTS/ CTS flow control at 9600-38400 bps. EIA/TIA-232E compatible at 9600, 19200, 38400, 57600 bps. Group III, Class 2 or 2.0 facsimile, (wired only). Operating Modes Advisory Mode (SAS:) Provides all features available except manual defibrillation, synchronous cardioversion, pacing, and access to previous patient records. Manual Mode: Provides normal operating capability for ALS users. Archive Mode: Allows operator to transmit, print, edit, or delete previous patient records. Setup Mode: Allows operator to configure the instrument. Service Mode: Allows operator to execute device diagnostic tests and calibrations. Inservice Mode: Provides simulated waveforms and trend graphs for demonstration purposes. Power Battery Only Configuration Choice of NiCd (FASTPAK or FASTPAK 2 battery, LIFEPAK NiCd battery 1.7 Ah or 2.4 Ah3) or SLA (LIFEPAK SLA battery) Dual battery capability Optional external AC Power Adapter Batteries charge while device operates from Power Adapter Data Management The device captures and stores patient data, events (including waveforms and annotations), and continuous ECG waveform records in internal memory. The user can select and print reports and transfer the stored information via an internal modem and various serial transfer protocols. Report Types Three format types of CODE SUMMARY critical event record (short, medium, and long) •Initial ECG (except short format) •Auto vital sign measurements every 5 minutes 3-channel or 4-channel 12-lead ECG report Continuous ECG waveform records (transfer only) Trend Summary Vital Signs Summary Snapshot ECG Monitor ECG is monitored via several cable arrangements. A 3-wire cable is used for 3-lead ECG monitoring. A 5-wire cable is used for 7-lead ECG monitoring. A 10-wire cable is used for 12-lead acquisition. When the chest electrodes are removed, the 10-wire cable functions as a 4-wire cable. Standard paddles or QUIK-COMBO pacing / defibrillation/ECG electrodes or FAST-PATCH disposable defibrillation / ECG electrodes are used for paddles lead monitoring. Lead Selection Leads I, II, III, (3-wire ECG cable) Leads I, II, III, AVR, AVL, and AVF acquired simultaneously, (4-wire ECG cable) Leads I, II, III, AVR, AVL, AVF, and C-lead acquired simultaneously, (5-wire ECG cable) Leads I, II, III, AVR, AVL, AVF, V1, V2, V3, V4, V5, and V6 acquired simultaneously, (10-wire ECG cable) EGG Size: 4, 3, 2.5, 2, 1.5, 1, 0.5, 0.25 cm/mV (fixed at 1 cm/mV for 12-lead) Heart Rate Display 20–300 bpm digital display Accuracy: ±4% or ±3 bpm, whichever is greater Out of range indication: Display symbol “---” Heart symbol flashes for each QRS detection QRS Detection Range Duration: 40 to 120 ms Amplitude: 0.5 to 5.0 mV Continuous Patient Surveillance System (CPSS) In advisory mode, while Shock Advisory System is not active, CPSS monitors the patient, via QUIK-COMBO paddles or Lead II ECG, for potentially shockable rhythms. Voice Prompts: Used for selected warnings and alarms (configurable on/off). Analog ECG Output: 1V/mV x 1.0 gain Common Mode Rejection: 90 dB at 50/60 Hz SpO2 (Masimo Sensors) Saturation Range: 1 to 100% Saturation Accuracy Adults/Pediatrics: ±2 digits (during no motion conditions); ±3 digits (during motion conditions) Neonates ±3 digits (during no motion conditions); ±3 digits (during motion conditions) Dynamic signal strength bar graph Pulse tone at the onset of the pleth waveform SpO2 Update Averaging Rate: User selectable 4, 8, 12 or 16 seconds SpO2 measurement: Functional SpO2 values are displayed and stored Pulse rate range: 25 to 240 pulses per minute Pulse Rate Accuracy Adults / Pediatrics / Neonates: ±3 digits (during no motion conditions); ±5 digits (during motion conditions) SpO2 waveform with autogain control Nellcor sensors when used with MNC-1 adapter NIBP Blood Pressure Systolic Pressure range: 30 to 245 mmHg (4 to 32.7 kPa) Diastolic Pressure range: 12 to 210 mmHg (1.6 to 28 kPa) Mean Arterial Pressure range: 20 to 225 mmHg (2.7 to 30 kPa) Units: mmHg, kPa, (user configurable) Blood Pressure Accuracy: maximum mean error of ±5 mmHg (±0.7 kPa) with a standard deviation no greater than ±8 mmHg (±1.1 kPa) Blood pressure measurement: 40 seconds, typical Pulse Rate Pulse Rate range: 30 to 200 pulses per minute Pulse Rate accuracy: ±2 pulses per minute or ±2%, whichever is greater Operation Features Initial Cuff Pressure: User selectable, 100 to 180 mmHg Automatic Measurement Time Interval: User selectable Automatic Cuff Deflation Excessive Pressure: If cuff pressure exceeds 300 mmHg Excessive Time: If measurement time exceeds 120 seconds CO2 CO2 Range: 0 to 99 mmHg (0 to 13.2 kPa); Units: mmHg, kPa, % (user configurable) CO2 Accuracy (0 to 20 minutes): 0 to 38 mmHg (0 to 5.1 kPa): ±4 mmHg; 39 to 99 mmHg (5.2 to 13.2 kPa): ±12% of reading CO2 Accuracy (>20 minutes): 0 to 38 mmHg (0 to 5.1 kPa): ±2 mmHg; 39 to 99 mmHg (5.2 to 13.2 kPa): ±5% of reading; +0.08% for every 1 mmHg (0.13 kPa) above 38 mmHg Respiration Rate Range: 0 to 60 breaths/minute Respiration Rate Accuracy: 0 to 40 bpm: ±1 bpm; 41 to 60 bpm: ±2 bpm Warm up time: 30 seconds (typical), 180 seconds maximum Rise Time: 190 ms Response Time: 2.9 seconds (includes delay time and rise time) Ambient Pressure: Automatically compensated internally Optional Display Waveform: CO2 Pressure IP Transducer Type: Strain-gauge resistive bridge Transducer Sensitivity: 5μV/V/mmHg Excitation Voltage: 5Vdc Connector: Electro Shield CXS 3102A 14S-6S Bandwidth: Digital filtered, dc to 30 Hz (< -3db) Zero Drift: 1 mmHg/hr without transducer drift Zero Adjustment: ±150 mmHg including transducer offset Numeric Accuracy: ±1 mmHg or 2% of reading, whichever is greater, plus transducer error Pressure Range: -30 to 300 mmHg in six user selectable settings Pulse Range: Pulse rate not derived from IP, IP monitor functions over the full ECG/SpO2/NIBP HR/PR range of 20–300 bpm Leakage Current: Meets ANSI/AAMI/IEC leakage requirements IP Connector Pinout: Counterclockwise from 12 o’clock, viewed from the front of LIFEPAK 12: A pin = -signal; B pin = +excitation; C pin = +signal; D pin = -excitation; E pin = shield; F pin = unlabeled. Invasive Pressure Display Display: IP waveform and numerics Units: mmHg, kPa (user configurable) Labels: P1 or P2, ART, PA, CVP, ICP, LAP (user selectable) Trend Display: Choice of HR, SpO2 (%), EtC02, FiCO2, RR, NIBP, P1, P2, STM shown in Channels 2 or 3 Time Scale: Auto, 30 minutes, 1, 2, 4, or 8 hours Duration: Up to 8 hours with -06 or later Memory PCB. Reduced storage capacity with earlier versions. ST After initial 12-lead ECG analysis, automatically selects and trends ECG lead with the greatest ST displacement Alarms Quick Set: Activates alarms for all parameters VF/VT Alarm: Activates continuous CPSS monitoring in Manual Mode Apnea Alarm: Occurs when 30 seconds has elapsed since last detected respiration Heart Rate Alarm Limit Range: Upper, 100–250 bpm; lower, 30–150 bpm Interpretive Algorithms 12-Lead Interpretive Algorithm: GE Medical 12SL, includes AMI statements Printer Prints continuous strip of the displayed patient information Paper Size: 50 mm (2.0 in) or optional 100 mm (3.9 in) Print Speed: 25 mm/Sec ±5% (measured in accordance with AAMI EC-11, 4.2.5.2) Optional 50 mm/sec time base for 12-Lead ECG reports Delay: 8 seconds Autoprint: Waveform events print automatically (user-configurable) Frequency Response Diagnostic Frequency Response: 0.05 to 150 Hz or 0.05 to 40 Hz (user-configurable) Monitor Frequency Response: 0.67 to 40 Hz or 1 to 30 Hz (user-configurable) Paddles Frequency Response: 2.5 to 30 Hz Analog ECG Output Frequency Response: 0.67 to 32 Hz (except 2.5 to 25 Hz for Paddles ECG and 1.3 to 23 Hz for 1 to 30 Hz Monitor Frequency Response)

Additional Information

General Information About Defibrillators Why Defibrillation? Sudden Cardiac Arrest (SCR)-Rapid irregular rhythm causing heart to quiver Cause: Ventricular Fibrillation (VF) Can lead to death if emergency shock not delivered Defibrillation – to counteract fibrillation Defibrillator Device used to administer an electric current (shock) to the heart Types of Defibrillators Manual external Manual Internal Automated External (AED) Semi-Automated External Implantable Cardioverter-Defibrillator (ICD) Manual External Defibrillator Widely used in Hospitals and clinics Inbuilt EKG reader Clinician Diagnoses the condition and accordingly administers the shock through paddles or pads Manual Internal Defibrillator Exclusively used in Operation Theatres Charge delivered through internal paddles in direct contact with the heart Automated External Defibrillator (AED) Used by lay persons requiring little training Built in heart rhythm analyzer Advices whether shock is required Semi-Automated External Defibrillators Used by paramedics and emergency medical technicians Automated capabilities of AED With ECG display and manual over ride option Implantable Cardioverter Defibrillator Implants similar to pacemakers Constantly monitor heart rhythm Automatically administers shock for arrhythmias Types of waveform - Shape of defibrillation current Monophasic damped sine waveform – delivers energy in one direction Relies on adjustment of joule settings Biphasic damped sine waveform – bi-directional current flow Measures impedance of patient and delivers precise dose of electricity Uses significantly low energy levels Decreases risk of burn in Myocardial damage