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HeartStart FR3 Defibrillator

HeartStart FR3

Defibrillator

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The HeartStart FR3 is Philips best professional-grade AED with advanced features for the professional responder.

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Features
Easy to use so you’re fast to respond
Easy to use so you’re fast to respond

Easy to use so you’re fast to respond

The FR3 is fast to use with peel and place SMART Pads III that are suitable for adults and children. It’s small, lightweight, and can be maneuvered in tight places. Quick Shock reduces the time between hands-off and shock delivery. And responders can quickly disconnect the FR3 and reconnect to the HeartStart MRx for a fast hand-off to the next level of care.
Rich clinical information to drive patient care
Rich clinical information to drive patient care

Rich clinical information to drive patient care

The FR3 delivers patient-specific guidance for the most appropriate initial therapy. For non-cardiac arrest patients, using the 3-Lead ECG cable helps you assess their condition. You get the information you need for confident decision-making. Plus, Philips add-on data management solutions help support a culture of continuous improvement and excellence.
Built to endure and designed for flexibility
Built to endure and designed for flexibility

Built to endure and designed for flexibility

The FR3 is built for harsh environments. It is tested to stringent military standards, meets IP55 rating for protection against dust and jetting water, and passes a 1,100 pound crush test. Plus, FR3 is a highly flexible platform so you can configure it for a wide range of current and evolving protocols.
  • Easy to use so you’re fast to respond
  • Rich clinical information to drive patient care
  • Built to endure and designed for flexibility
See all features
Easy to use so you’re fast to respond
Easy to use so you’re fast to respond

Easy to use so you’re fast to respond

The FR3 is fast to use with peel and place SMART Pads III that are suitable for adults and children. It’s small, lightweight, and can be maneuvered in tight places. Quick Shock reduces the time between hands-off and shock delivery. And responders can quickly disconnect the FR3 and reconnect to the HeartStart MRx for a fast hand-off to the next level of care.
Rich clinical information to drive patient care
Rich clinical information to drive patient care

Rich clinical information to drive patient care

The FR3 delivers patient-specific guidance for the most appropriate initial therapy. For non-cardiac arrest patients, using the 3-Lead ECG cable helps you assess their condition. You get the information you need for confident decision-making. Plus, Philips add-on data management solutions help support a culture of continuous improvement and excellence.
Built to endure and designed for flexibility
Built to endure and designed for flexibility

Built to endure and designed for flexibility

The FR3 is built for harsh environments. It is tested to stringent military standards, meets IP55 rating for protection against dust and jetting water, and passes a 1,100 pound crush test. Plus, FR3 is a highly flexible platform so you can configure it for a wide range of current and evolving protocols.
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Final CEE consent

Features

fr3 features img 1

CPR Quality

  • Quick shock reduces the time between hands-off and shock delivery
 
Case
  • Small, light, and easy-to-maneuver in tight places
  • Tested to military standards and is US Army Airworthiness Release (AWR) certified
Pads
  • Pre-connected pads with no pouch to open
  • Easily hands off to Philips MRx defibrillator-monitor
  • Pads can be used on adults and children
  • Infant/Child Key automatically adjusts therapy for infant/child protocols
 
Software
  • Integrates with Philips data management software solutions
 
Battery
  • Delivers 300 shocks or 10 hours (with QCPR) of monitoring if configured

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Specifications

SMART Pads III
SMART Pads III
Application
  • Peel and place pads can be removed from packaging and stored in carry case.
Automated and user-activated self-tests
Automated and user-activated self-tests
Function
  • Places FR3 into a scenario-based training mode and simulates shock therapy
Type
  • 10.8 Volt, 4.5 Ah Li-ion battery
Environment/physical
Environment/physical
Altitude
  • Meets IEC 60601-1:5.3 (1013 to 572 mbar (hPa), equivalent to air pressure from 0 to 15,000 feet; 0 to 4,572 meters) m
Vibration
  • Meets MIL-STD-810F 514.5 C-17
Sealing
  • Meets IEC529 class IP55 with battery installed
Temperature
  • Operating/standby: 32°–122°F (0°– 50°C)
Shock/drop
  • Meets MIL-STD-810F 516.5, Procedure IV (after a one-meter drop to any edge, corner, or surface in standby mode)
Defibrillator
Defibrillator
Models
  • Models 861388 text display 861389 ECG and text display
Indicators
  • High-rez LCD, beeper, voice prompts, tones, speaker, connector socket, ready light, shock button
Waveform
  • SMART Biphasic Truncated Exponential waveform parameters adjust as a function of patient impedance.
Advanced mode
  • Advanced mode Configurable using optional HeartStart Configure software
Shock delivery
  • Via defibrillator pads placed in the anterior-anterior position for adults, infants and children.
FR3 primary battery
FR3 primary battery
Type
  • Type 12 VDC, 4.7 Ah, lithium manganese dioxide Long-life primary cells
Standby life
  • 3 years minimum when stored under standby environmental conditions (battery installed)
Shelf life
  • 5 years
Capacity
  • Please consult User’s Manual for capacity specifications.
Infant/Child Key
Infant/Child Key
Function
  • Selects therapy for infants or children under 55 lbs (25 kg) or 8 years old
Physical
Physical
Size
  • 2.7˝ high x 5.3˝ wide x 8.7˝ deep (6.9 cm x 13.5 cm x 22.1 cm)
Weight
  • 3 lbs 8 oz (1.6 kg) with FR3 primary battery installed
FR3 data card
FR3 data card
Function
  • Function Stores a minimum of 8 hours of ECG, event, and, if configured, voice recording.
Environmental/Physical Requirements
Environmental/Physical Requirements
Operating Altitude
  • Meets IEC 60601-1:5.3 (1013 to 572 mbar (hPa), equivalent to air pressure from 0 to 15,000 feet; 0 to 4,572 meters)
Operating Temperature
  • Operating/standby: 32°–122°F (0°– 50°C)
Shock/Drop Abuse Tolerance
  • Meets MIL-STD-810F 516.5, Procedure IV (after a one-meter drop to any edge, corner, or surface in standby mode)
Sealing
  • Meets IEC529 class IP55 with battery installed
Vibration
  • Meets MIL-STD-810F 514.5 C-17
ECG display
ECG display
Bandwidth
  • Bandwidth 1 Hz to 30 Hz (-3dB), nominal (non-diagnostic)
Monitored Lead
  • Monitored lead Lead II using anterior-anterior adult pads placement
Screen
  • Screen LCD color display, 320 x 240 pixels. 2.8˝ x 2.1˝ (7.2 cm x 5.4 cm)
Patient analysis system
Patient analysis system
ECG analysis
  • Evaluates impedance of pads for contact, ECG rhythm and signal quality; detect artifact & pacemaker
Quick Shock
  • Typically arms in 8 seconds from the end of the “Stop CPR” prompt
Sensitivity/specificity
  • Meets AAMI DF80 requirements and AHA recommendations for adult defibrillation
SMART CPR
  • Evaluates key characteristics of the presenting VF and determines the initial therapy.
SMART Pads III
SMART Pads III
Application
  • Peel and place pads can be removed from packaging and stored in carry case.
Automated and user-activated self-tests
Automated and user-activated self-tests
Function
  • Places FR3 into a scenario-based training mode and simulates shock therapy
Type
  • 10.8 Volt, 4.5 Ah Li-ion battery
See all specifications
SMART Pads III
SMART Pads III
Application
  • Peel and place pads can be removed from packaging and stored in carry case.
Automated and user-activated self-tests
Automated and user-activated self-tests
Function
  • Places FR3 into a scenario-based training mode and simulates shock therapy
Type
  • 10.8 Volt, 4.5 Ah Li-ion battery
Environment/physical
Environment/physical
Altitude
  • Meets IEC 60601-1:5.3 (1013 to 572 mbar (hPa), equivalent to air pressure from 0 to 15,000 feet; 0 to 4,572 meters) m
Vibration
  • Meets MIL-STD-810F 514.5 C-17
Sealing
  • Meets IEC529 class IP55 with battery installed
Temperature
  • Operating/standby: 32°–122°F (0°– 50°C)
Shock/drop
  • Meets MIL-STD-810F 516.5, Procedure IV (after a one-meter drop to any edge, corner, or surface in standby mode)
Defibrillator
Defibrillator
Models
  • Models 861388 text display 861389 ECG and text display
Indicators
  • High-rez LCD, beeper, voice prompts, tones, speaker, connector socket, ready light, shock button
Waveform
  • SMART Biphasic Truncated Exponential waveform parameters adjust as a function of patient impedance.
Advanced mode
  • Advanced mode Configurable using optional HeartStart Configure software
Shock delivery
  • Via defibrillator pads placed in the anterior-anterior position for adults, infants and children.
FR3 primary battery
FR3 primary battery
Type
  • Type 12 VDC, 4.7 Ah, lithium manganese dioxide Long-life primary cells
Standby life
  • 3 years minimum when stored under standby environmental conditions (battery installed)
Shelf life
  • 5 years
Capacity
  • Please consult User’s Manual for capacity specifications.
Infant/Child Key
Infant/Child Key
Function
  • Selects therapy for infants or children under 55 lbs (25 kg) or 8 years old
Physical
Physical
Size
  • 2.7˝ high x 5.3˝ wide x 8.7˝ deep (6.9 cm x 13.5 cm x 22.1 cm)
Weight
  • 3 lbs 8 oz (1.6 kg) with FR3 primary battery installed
FR3 data card
FR3 data card
Function
  • Function Stores a minimum of 8 hours of ECG, event, and, if configured, voice recording.
Environmental/Physical Requirements
Environmental/Physical Requirements
Operating Altitude
  • Meets IEC 60601-1:5.3 (1013 to 572 mbar (hPa), equivalent to air pressure from 0 to 15,000 feet; 0 to 4,572 meters)
Operating Temperature
  • Operating/standby: 32°–122°F (0°– 50°C)
Shock/Drop Abuse Tolerance
  • Meets MIL-STD-810F 516.5, Procedure IV (after a one-meter drop to any edge, corner, or surface in standby mode)
Sealing
  • Meets IEC529 class IP55 with battery installed
Vibration
  • Meets MIL-STD-810F 514.5 C-17
ECG display
ECG display
Bandwidth
  • Bandwidth 1 Hz to 30 Hz (-3dB), nominal (non-diagnostic)
Monitored Lead
  • Monitored lead Lead II using anterior-anterior adult pads placement
Screen
  • Screen LCD color display, 320 x 240 pixels. 2.8˝ x 2.1˝ (7.2 cm x 5.4 cm)
Patient analysis system
Patient analysis system
ECG analysis
  • Evaluates impedance of pads for contact, ECG rhythm and signal quality; detect artifact & pacemaker
Quick Shock
  • Typically arms in 8 seconds from the end of the “Stop CPR” prompt
Sensitivity/specificity
  • Meets AAMI DF80 requirements and AHA recommendations for adult defibrillation
SMART CPR
  • Evaluates key characteristics of the presenting VF and determines the initial therapy.

Documentation

Application notes (1)

Application notes

Customer story (1)

Customer story

Product news (1)

Product news

Application notes (1)

Application notes

Customer story (1)

Customer story

See all documentation

Application notes (1)

Application notes

Customer story (1)

Customer story

Product news (1)

Product news

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