Physio-Control LIFEPAK 15 Monitor / Defibrillator in the USA & India

Description

The Physio-Control LIFEPAK 15 Monitor / Defibrillator is an advanced, reliable defibrillator with a clear display and many capabilities to tak advantage of. This defibrillator is available in several configurations to suit many emergency needs. Please see the "Configurations" tab for more details to make the best selection for you.

Note: Carry case pictured above is NOT included with unit.

Warranty: 5 Years - Free from Defects in Material and Workmanship.

The LIFEPAK 15 Monitor / Defibrillator has six convenient operating modes for setting up the device for your needs:

AED Mode: Automated ECG analysis and prompted treatment protocol for patients in cardiac arrest.
Manual Mode: Manual defibrillation, noninvasive pacing, ECG and vital signs monitoring, and synchronized cardioversion.
Archive Mode: Access stored patient information.
Setup Mode: Change default settings to operation.
Service Mode: For performing diagnostic texts and calibrations before use.
Demo Mode: Simulated waveforms and trend graphs for demonstrations and training

The LIFEPAK 15 display is a dual-mode, 8.4-inch, LCD screen with SunVue, which displays clearly in full glare sunlight from any angle. In terms of power, this monitor / defibrillator runs off a two-battery system featuring long-lasting lithium-ion batteries. The LIFEPAK 15 charging system includes a base charger, adapter tray, and the batteries for a quick and easy recharge system when the device is not in use.

On the exterior of the device is a large carry handle for trade-offs, clearly labeled buttons, and room for accessories. These accessories can include the basic carry case, shoulder strap, attachable storage pouches, and more. Please note that accessories are NOT included with the device and must be purchased separately. For a full list of compatible products, see the "Accessories" tab for more details.

This device is incredibly durable. It can survive 30 inch drops (which is roughly the height of most stretchers), wind, rain, and other harsh weather conditions. The screen is double-layer to withstand knocks and scrapes and the handle is shock-absorbing.

Physio-Control LIFEPAK 15 Monitor / Defibrillator Features

Extremely durable, shock-absorbing, and double-layered screen.
Rechargeable battery packs.
LCD Display with SunVue for glare-free visuals.
Accessories for purchase include a carry case, shoulder strap, and attachable pouches,
Extremely customizable variations, see Configurations to determine which one is best for you.

Physio-Control LIFEPAK 15 Monitor / Defibrillator Specifications

Physical Characteristics

Weight:
- Basic monitor/defibrillator with new roll paper and two batteries installed: 17.5 lbs (7.9 kg).
- Fully featured monitor/defibrillator with new roll paper and two batteries installed: 18.5 lbs (8.4 kg).
Lithium-ion Battery: ≤ 1.3 lbs (0.6 kg).
Accessory Bags and Shoulder Strap: 3.9 lbs (1.77 kg).
Standard (hard) Paddles: 2.1 lbs (0.95 kg).
Height: 12.5 in (31.7 cm).
Width: 15.8 in (40.1 cm).
Depth: 9.1 in (23.1 cm).

Display Specifications

Size (active viewing area): 8.4 in (212 mm) diagonal; 6.7 in (171 mm) wide x 5 in (128 mm) high.
Resolution: display type 640 dot x 480 dot color backlit LCD
User Selectable Display Mode: full color or SunVue™ display high contrast.
Display: a minimum of 5 seconds of ECG and alphanumerics for values, device instructions, or prompts, up to three waveforms.
Waveform Display Sweep Speed: 25 mm/sec for ECG, Sp0₂, IP, and 12.5 mm/sec for CO₂.

Data Management

Report Types:
- Three format types of CODE SUMMARY™ critical event
  record: short, medium, and long.
- 12-lead ECG with STEMI statements.
- Continuous Waveform (transfer only).
- Trend Summary.
- Vital Sign Summary.
- Snapshot.
Memory Capacity: Total capacity is 360 minutes of continuous ECG, 90 minutes of continuous data from all channels, or 400 single waveform events.
Maximum memory capacity for a single patient includes up to 200 single waveform reports and 90 minutes of continuous ECG.

Monitor

ECG
- Frequency Response:
  - Monitor: 0.5 to 40 Hz or 1 to 30 Hz
  - Paddles: 2.5 to 30 Hz
  - 12-lead ECG diagnostic: 0.05 to 150 Hz
- 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)
- ECG 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
  - QRS Detection Range Duration: 40 to 120 msec
  - Amplitude: 0.5 to 5.0 m
- Common Mode Rejection (CMRR): ECG Leads: 90 dB at 50/60 Hz
Sp0₂/SpC0/SpMet
- Sensors:
  - MASIMO® sensors including RAINBOW® sensors
  - NELLCOR® sensors when used with the MASIMO RED™ MNC adapter
Sp0₂
- Displayed Saturation Range: “<50” for levels below 50%; 50 to 100%
- Saturation Accuracy: 70–100% (0–69% unspecified)
- Adults/Pediatrics:
  - ±2 digits (during no motion conditions)
  - ±3 digits (during motion conditions)
  - Dynamic signal strength bar graph
  - Pulse tone as Sp02 pulsations are detected
- Sp02 Update Averaging Rate User selectable: 4, 8, 12 or 16 seconds
- Sp02 Sensitivity User selectable: Normal, High
- Sp02 Measurement: Functional Sp02 values are displayed and stored
- Pulse Rate Range: 25 to 240 bpm
- Pulse Rate Accuracy (Adults/Pediatrics):
  - ±3 digits (during no motion conditions)
  - ±5 digits (during motion conditions)
  - Optional Sp02 waveform display with autogain control
SpCO
- SpC0 Concentration Display Range: 0 to 40%
- SpC0 Accuracy: ±3 digits
SpMET
- SpMet Saturation Range: 0 to 15.0%
- SpMet Display Resolution: 0.1% up to 10%
- SpMet Accuracy: ±1 digit
NIBP
- Blood Pressure Systolic Pressure Range: 30 to 255 mmHg
- Diastolic Pressure Range: 15 to 220 mmHg
- Mean Arterial Pressure Range: 20 to 235 mmHg
- Units: mmHg
- Blood Pressure Accuracy: ±5 mmHg
- Blood Pressure Measurement Time: 20 seconds, typical (excluding cuff inflation time)
- Pulse Rate Range: 30 to 240 pulses per minute
- Pulse Rate Accuracy: ±2 pulses per minute or ±2%, whichever is greater
- Operation Features Initial Cuff Pressure: User selectable, 80 to 180 mmHg
- Automatic Measurement Time Interval: User selectable, from 2 min to 60 min
- Automatic Cuff Deflation Excessive Pressure: If cuff pressure exceeds 290 mmHg
- Excessive Time: If measurement time exceeds 120 seconds
CO₂
- CO₂ Range: 0 to 99 mmHg (0 to 13.2 kPa)
- Units: mmHg, %, or kPa
- Respiration Rate Accuracy:
  - 0 to 70 bpm: ±1 bpm
  - 71 to 99 bpm: ±2 bpm
- Respiration Rate Range: 0 to 99 breaths/minute
- Rise Time: 190 msec
- Response Time: 3.3 seconds (includes delay time and rise time)
- Initialization Time: 30 seconds (typical), 10-180 seconds
- Ambient Pressure: automatically compensated internally
- Optional Display: CO2 pressure waveform
  - Scale factors: Autoscale, 0–20 mmHg (0–4 Vol%), 0–50 mmHg (0–7 Vol%), 0–100 mmHg (0–14 Vol%)
Invasive Pressure
- Transducer Type: Strain-gauge resistive bridge
- Transducer Sensitivity: 5μV/V/mmHg
- Excitation Voltage: 5 Vdc
- 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 ranges
Invasive Pressure Display
- Display: IP waveform and numerics
- Units: mmHg
- Labels: P1 or P2, ART, PA, CVP, ICP, LAP (user selectable)
Temperature
- Range: 24.8° to 45.2°C (76.6° to 113.4°F)
- Resolution: 0.1°C
- Accuracy: ±0.2°C including sensor
- Reusable Temperature Cable: 5 foot or 10 foot
- Disposable Sensor Types: Surface–Skin; Esophageal/Rectal
Trend
- Time Scale: Auto, 30 minutes, 1, 2, 4, or 8 hours
- Duration: Up to 8 hours
- ST Segment: After initial 12-lead ECG analysis, automatically selects and trends ECG lead with the greatest ST displacement
- Display Choice of: HR, PR (SpO2), PR (NIBP), SpO2 (%), SpCO (%), SpMet (%), CO2 (EtCO2/FiCO2), RR (CO2), NIBP, IP1, IP2, ST

Alarms

Quick Set: Activates alarms for all active vital signs
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 Algorithm

12-Lead Interpretive Algorithm: University of Glasgow 12-Lead ECG Analysis Program, includes AMI and STEMI statements

Printer

Prints continuous strip of the displayed patient information and reports
Paper Size: 100 mm (3.9 in)
Print Speed: 25 mm/sec or 12.5 mm/sec
- Optional: 50 mm/sec time base for 12-lead ECG reports
Delay: 8 seconds
Autoprint: Waveform events print automatically
Frequency Response:
- Diagnostic: 0.05 to 150 Hz or 0.05 to 40 Hz
- Monitor: 0.67 to 40 Hz or 1 to 30 Hz

Defibrillator

Biphasic Waveform: Biphasic Truncated Exponential
The following specifications apply from 25 to 200 ohms, unless otherwise specified:
Energy Accuracy: ±1 joule or 10% of setting, whichever is greater, into 50 ohms, ±2 joules or 15% of setting, whichever is greater, into 25-175 ohms.
Voltage Compensation: Active when disposable therapy electrodes are attached. Energy output within ±5% or ±1 joule, whichever is greater, of 50 ohms value, limited to the available energy which results in the delivery of 360 joules into 50 ohms.
Paddle Options: QUIK-COMBO® pacing/defibrillation/ECG electrodes (standard). Cable Length 8 foot long (2.4 m)
QUIK-COMBO cable (not including electrode assembly).
Standard paddles (optional)
Manual Mode:
- Energy Select: 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 30, 50, 70, 100, 125, 150, 175, 200, 225, 250, 275, 300, 325, and 360 joules
- Charge Time: Charge time to 360 joules in less than 10 seconds, typical
- Synchronous Cardioversion: Energy transfer begins within 60 msec of the QRS peak
- Paddles Leads OFF Sensing: When using QUIK-COMBO electrodes, the device indicates Paddles Leads OFF if the resistive part of the patient impedance is greater than 300 ±15% ohms, or if the magnitude of the patient impedance is greater than 440 ±15% ohms.
AED Mode:
- Shock Advisory System™ (SAS): an ECG analysis system that advises the operator if the algorithm detects a shockable or non-shockable ECG rhythm. SAS acquires ECG via therapy electrodes only.
- Shock Ready Time: Using a fully charged battery at normal room temperature, the device is ready to shock within 20 seconds if the initial rhythm finding is “SHOCK ADVISED”
- Biphasic Output: Energy Shock levels ranging from 150–360 joules with same or greater energy level for each successive shock cprMAX™ Technology: In AED mode, cprMAX™ technology provides a method of maximizing the CPR time that a patient receives, with the overall goal of improving the rate of survival of patients treated with AEDs.
- Setup Options:
  - Auto Analyze: Allows for auto analysis. Options are OFF, AFTER 1ST SHOCK
  - Initial CPR: Allows the user to be prompted for CPR for a period of time prior to other activity. Options are OFF, ANALYZE FIRST, CPR FIRST
  - Initial CPR Time: Time interval for Initial CPR. Options are 15, 30, 45, 60, 90, 120, and 180 seconds.
  - Pre-Shock CPR: Allows the user to be prompted for CPR while the device is charging. Options are OFF, 15, 30 seconds.
  - Pulse Check: Allows the user to be prompted for a pulsecheck at various times. Options are ALWAYS, AFTER EVERY SECOND NSA, AFTER EVERY NSA, NEVER
  - Stacked Shocks: Allows for CPR after 3 consecutive shocks or after a single shock. Options are OFF, ON
  - CPR Time: 1 or 2 User selectable times for CPR. Options are 15, 30, 45, 60, 90, 120, 180 seconds and 30 minutes.

Pacer

Pacing Mode: Demand or non-demand rate and current defaults
Pacing Rate: 40 to 170 PPM
Rate Accuracy: ±1.5% over entire range
Output Waveform: Monophasic, truncated exponential current pulse (20 ± 1 ms)
Output Current: 0 to 200 mA
Pause: Pacing pulse frequency reduced by a factor of 4 when activated
Refractory Period: 180 to 280 msec (function of rate)

Environmental

Unit meets functional requirements during exposure to the following environments unless otherwise stated.
Operating Temperature: 0° to 45°C (32° to 113°F); -20°C (-4°F) for 1 hour after storage at room temperature; 60°C (140°F) for 1 hour after storage at room temperature
Storage Temperature: -20° to 65°C (-4° to 149°F) except therapy electrodes and batteries
Relative Humidity, Operating: 5 to 95%, non-condensing. NIBP: 15 to 95%, non-condensing
Relative Humidity, Storage: 10 to 95%, non-condensing
Atmospheric Pressure, Operating: -382 to 4,572 m (-1,253 to 15,000 ft). NIBP: -152 to 3,048 m (-500 to 10,000 ft)
Water Resistance, Operating: IP44 (dust and splash resistance) per IEC 529 and EN 1789 (without accessories except for 12-lead ECG cable, hard paddles, and battery pack)
Vibration: MIL-STD-810E Method 514.4, Propeller Aircraft - category 4 (figure 514.4-7 spectrum a), Helicopter - category 6 (3.75 Grms), Ground Mobile - category 8 (3.14 Grms), EN 1789: Sinusoidal Sweep, 1 octave/min, 10-150 Hz, ±0.15 mm/2 g
Shock (drop): 5 drops on each side from 18 inches onto a steel surface EN 1789: 30-inch drop onto each of 6 surfaces
Shock (functional): Meets IEC 60068-2-27 and MIL-STD-810E shock requirements 3 shocks per face at 40 g, 6 ms half-sine pulses
Bump: 1000 bumps at 15 g with pulse duration of 6 msec
Impact, Non-operating: EN 60601-1 0.5 + 0.05 joule impact UL 60601-1 6.78 Nm impact with 2-inch diameter steel ball. Meets IEC62262 protection level IK 04.
EMC: EN 60601-1-2:2006 Medical Equipment - General Requirements for Safety - Collateral Standard: Electromagnetic Compatibility - Requirements and Tests EN 60601-2-4:2003: (Clause 36) Particular Requirements for the Safety of Cardiac Defibrillators and Cardiac Defibrillator-Monitors
Cleaning: Cleaning 20 times with the following: Quaternary ammonium, isopropyl alcohol, hydrogen peroxide
Chemical Resistance: 60 hour exposure to specified chemicals: Betadine (10% Povidone-Iodine solution), Coffee, Cola, Dextrose (5% Glucose solution), Electrode Gel/Paste (98% water, 2% Carbopol 940), HCL (0.5% solution, pH=1), Isopropyl Alcohol, NaCl solution (0.9% solution), Cosmetic discoloration of the paddle well shorting bar shall be allowed following exposure to HCL (0.5% solution).

Power

Power Adapters: AC or DC
Power Adapters provide operation and battery charging from external AC or DC power
- Full functionality with or without batteries when connected to external AC/DC
- Typical battery charge time while installed in LIFEPAK 15 device is 190 minutes
- Indicators: external power indicator, battery charging indicator
Dual battery: Capability with automatic switching
Low battery indication and message: Low battery fuel gauge indication and low battery message in status area for each battery
Replace battery indication and message: Replace battery fuel gauge indication, audio tones and replace battery message in the status area for each battery. When replace battery is indicated, device auto-switches to second battery. When both batteries reach replace battery condition, a voice prompt instructs user to replace battery.

Battery

Battery Type: Lithium-ion
Weight: ≤0.6kg (1.3lb)
Charge Time (with fully depleted battery): 4 hours and 15 minutes (typical)
Battery indicators: Each battery has a fuel gauge that indicates its approximate charge. A fuel gauge that shows two or fewer LEDs after a charge cycle indicates that the battery should be replaced.
Charging Temperature Range: 5° to 45°C (41° to 113°F)
Operating Temperature Range: 0° to 45°C (32° to 113°F)
Short Term (<1 week) Storage Temperature Range: -20° to 60°C (-4° to 140°F)
Long Term (>1 week) Storage Temperature Range: 20° to 25°C (68° to 77°F)
Operating and Storage Humidity Range: 5 to 95% relative humidity, non-condensing