The Physio-Control Lifepak 12 is a defibrillator/monitor with pacing options. The Lifepak 12 offers both manual and semi-automatic external defibrillation monitors along with an Add mode. The defibrillator comes with a Shock advisory system to help detect rhythm for shocking, along with a simple 1-2-3 operation. With a large LDC screen, 3 ECG channels can be simultaneously viewed with up to 8 seconds of cascading ECG. Additionally, the Lifepak 12 can also monitor parameters such as heart rate, pulse oximetry, oxygen, blood pressure, and additional vital. The system can easily be connected to Bluetooth to transfer ECG reading and patient data.
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
- Lifepak 12 Paddle accessories
- Electroluminescent (EL) display (The optimal viewability of an EL display is compromised in direct sunlight.)
Features & Specifications
Physical
| Weight: |
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| Height: | 31.7 cm (12.5 in) |
| Width: | 38.9 cm (15.3 in) |
| Depth: | 21.7 cm (8.5 in) |
Display
| Size: |
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| Display Type: |
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Communications
| The Lifepak 12 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 on the Lifepak 12 |
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| 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 Lifepak 12. |
| Service Mode: | Allows operator to execute device diagnostic tests and calibrations on the Lifepak 12. |
| Inservice Mode: | Provides simulated waveforms and trend graphs for demonstration purposes. |
Power
| Battery Only Configuration: |
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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: |
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ECG Monitor
| ECG on the Lifepak 12 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: |
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| 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 on the Lifepak 12: |
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| QRS Detection Range: |
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| 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% |
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| 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 on the: | User selectable 4, 8, 12 or 16 seconds |
| SpO2 measurement on the: | 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 on the: |
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| Pulse Rate: |
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| Operation Features |
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| Automatic Cuff Deflation |
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CO2 on the
| CO2 Range: | 0 to 99 mmHg (0 to 13.2 kPa); Unit: mmHg, kPa, % (user configurable) |
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| 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 on the: | 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 on the: | Automatically compensated internally |
| Optional Display Waveform on the: | CO2 Pressure |
IP
| Transducer Type: | Strain-gauge resistive bridge |
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| Transducer Sensitivity: | 5μV/V/mmHg |
| Excitation Voltage on the: | 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 |
| 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 the Lifepak 12:
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| Invasive Pressure Display: |
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Trend
| Display: | Choice of HR, SpO2 (%), EtC02, FiCO2, RR, NIBP, P1, P2, STM shown in Channels 2 or 3 |
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| 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 of the. |
ST
| After initial 12-lead ECG analysis it automatically selects and trends ECG lead with the greatest ST displacement |
Alarms
| Quick Set: | Activates alarms for all parameters |
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| 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) |
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| 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) |
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| 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) |
Weight
Lifepak 12 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)
Lifepak 12 FASTPAK battery: 0.64 kg (1.4 lbs)
Lifepak 12 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 on the Lifepak 12
Displays a minimum of 4 seconds of ECG and alphanumerics for values, device instructions, or prompts.
Option to display one or two additional waveforms on the Lifepak 12
Waveform display sweep speed: 25 mm/sec for ECG, SpO2, IP, and 12.5 mm/sec for CO2
Communications
The Lifepak 12 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 on the Lifepak 12
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 Lifepak 12.
Service Mode: Allows operator to execute device diagnostic tests and calibrations on the Lifepak 12.
Inservice Mode: Provides simulated waveforms and trend graphs for demonstration purposes.
Power
Battery Only Configuration
Choice of NiCd (FASTPAK or FASTPAK 2 battery, 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 on the Lifepak 12 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 on the Lifepak 12
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 on the: User selectable 4, 8, 12 or 16 seconds
SpO2 measurement on the: 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 on the
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 on the: 20 to 225 mmHg (2.7 to 30 kPa)
Units: mmHg, kPa, (user configurable)
Blood Pressure Accuracy on the: 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 on the: 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 on the: If measurement time exceeds 120 seconds
CO2 on the
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 on the: 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 on the: Automatically compensated internally
Optional Display Waveform on the: CO2 Pressure
IP
Transducer Type: Strain-gauge resistive bridge
Transducer Sensitivity: 5μV/V/mmHg
Excitation Voltage on the: 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
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 the 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 of the.
ST
After initial 12-lead ECG analysis it 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) Warranty:
For new products, please refer to the manufacturer's website for details.
This product has been refurbished and tested to the highest quality standards by The PCB Medical. This Limited Warranty offered by PCB Medical covers defects in material or workmanship. This warranty extends to the original purchaser only and is nontransferable. The warranty begins the day the equipment is received. Please inspect your item(s) upon delivery. Any unauthorized service providers working on our equipment within the warranty period will void the warranty!
Our warranty periods are very based on product, a standard 30 day parts warranty is included with all refurbished parts unless stated otherwise on the quote/Invoice. Warranties begin from the documented date of receipt.
Our warranties do not cover any problem that is caused by: A. Conditions, malfunctions or damage not resulting from defects in material or workmanship. B. Conditions, malfunctions or damage resulting from (1) normal wear and tear, improper installation, improper maintenance, misuse, abuse, negligence, accident or alteration.
Our limited warranties are void if a product is returned with removed, damaged or tampered labels or any alterations (including removal of any component or external cover).
PCB Medical will not provide any warranty coverage unless claims are made in compliance with all terms of the controlling warranty statement included with your product and you follow proper return procedure. To request warranty service, you will need to provide: 1. The invoice or other evidence of the date and place of purchase. 2. A description of the problem. 3. Contact our Customer Service Department to receive a Return Authorization Number (RMA#)
Shipping and Returns:
Damaged freight needs to be reported within 24 hours to file a claim. No merchandise may be returned without prior written authorization by PCB Medical.
No NEW merchandise may be returned unless authorization from manufacturer which could result in a restocking fee or no return at all, and customer is responsible for shipping expenses.
Return period for products is thirty (30) days from delivery or otherwise agreed upon.
The PCB Medical will test returned products returned and can impose a customer fee if the customer misrepresents the condition of the product.
CREDIT AND RETURN SHIPPING GUIDELINES
Order cancellations (after 24 hours) and returns are charged a 45% restocking fee. Damaged goods will receive credit dependent on the condition of the product, and customer is responsible for shipping expenses.
No credit will be issued if the item is non-returnable, such as a new product, custom or special order, or in the case that the item is damaged due to improper handling/packaging by the customer.
Shipping Charges: Customers are responsible for making sure items can be delivered into or outside of their facility without issue. For example, can a 53’ foot truck access your building? Failure to accommodate delivery can result in items not being delivered, additional fees, or return of equipment.
Basic Shipping Charge is for dock to dock shipping and/or liftgate service shipping. The items shipping dock to dock and/or liftgate are skidded/palletized items. It doesn’t not include inside delivery.
Residential shipping charge is for customer’s needing delivery in a residential area.
Inside delivery is for customer’s needing their purchase delivered inside the building. The item(s) will be delivered into the lobby only. They are not delivered into rooms/suites, elevators, or stairs.
Customers are responsible for disposing of packing materials.
If you are needing white glove delivery, please contact us directly at INFO@pcbhme.com
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