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Each year sudden cardiac arrest (SCA) strikes approximately 340 thousand people in the
U.S. alone and hundreds of thousands more worldwide. Fewer than 5% of those victims survive, largely because emergency medical services do not reach them in time. The combination of timely CPR and defibrillation is a highly effective treatment for the most common form of SCA, significantly improving the chances of survival. Its host of features makes the FR2+ an extremely versatile and rugged defibrillator, enabling responders to potentially save the life of a coworker, friend, patient or fellow citizen under demanding circumstances. • Lightweight Weighs just under 5 pounds fully equipped |
| The HeartStart FR2+ has come to be a trusted tool of professional responders and designated response teams in the work place and public settings. Its clean, uncluttered design is optimized for fast, efficient operation and rapid delivery of defibrillation therapy. Commands are clear and concise: ideal for responders who are trained, drilled, and ready to help save a life now. The HeartStart FR2+ offers features that make hand-off to advanced life support (ALS) trained professionals seamless to ensure continuity of care for the patient. An ECG display is available, and the FR2+ can be configured to allow ALS responders to switch to a manual mode, giving them more decision-making control. And defibrillator pads adapters enable the pads to remain on the patient when transferring to many popular ALS manual defibrillators from Philips and other manufacturers. But don’t be misled by its advanced capabilities.The HeartStart FR2+ is extremely easy to use. Its design is based on years of research refined through Philips human factors experts, and user testing with the full range of responders, from healthcare professionals to lay people. In fact, hundreds of thousands of citizens are already trained and ready to help save a life with the FR2+. Optimized for challenging environments The HeartStart FR2+ is the right choice for harsh, outdoor, or mobile use. It combines natural sounding voice instructions that are loud and clear, with text prompts on a large, bright back-lit display.This makes it ideal if you anticipate use in noisy or poorly lit settings. And at just 4.7 pounds, it’s incredibly small and lightweight so it won’t weigh you down. Versatility The FR2+ is designed to be highly flexible and versatile.You can tailor your FR2+ to match your specific response protocol. Infant and child defibrillation. The FR2+ can treat patients of any age. When equipped with special infant/child defibrillator pads that reduce the energy of the FR2+’s shock to a more appropriate level, you can safely treat a child or infant in cardiac arrest. Conscious monitoring. The reusable 3-leadwire FR2+ ECG assessment module enables the professional responder to proactively use the FR2+ to assess the rhythm of patients who are not in cardiac arrest, but are conscious, breathing, and suspected of being at risk for cardiac distress.This small, lightweight monitoring solution is ideal for in- and out-of-hospital patient transport, bike medics, situations requiring long or difficult travel, fire rigs that may be staffed on occasion by paramedics, clinics and physicians’ offices. |
| Ready to use The HeartStar t FR2+ is reliable and virtually maintenance-free. It automatically performs daily, weekly, and monthly self-tests of the battery, electrical components, and subsystems. A highly visible status indicator shows at a glance whether the FR2+ has passed its last self-test and is ready for use. Reliable analysis technologies The FR2+ uses Philips' patented SMART Analysis algorithm to assess the patient's heart rhythm and determine if it is shockable. Research shows that for some patients, especially those in long-duration cardiac arrest, CPR prior to defibrillation may provide more benefit. At the discretion of the medical director, the defibrillator's SMART CPR algorithm can be configured to look at characteristics of a shockable heart rhythm and compute the likelihood that spontaneous circulation will return with an initial shock. Depending on the results, the caregiver is advised to provide either an immediate defibrillation shock or CPR first followed by a shock. Quick Shock Research also suggests that the opportunity for survival can be improved if interruptions to CPR are minimized. The Quick Shock capability of the FR2+ readies the defibrillator within seconds to deliver a shock, reducing the time between CPR and defibrillation. No other manufacturer can deliver a shock as quickly after CPR. Proven therapy When a shock is advised, the FR2+ prompts the user to deliver Philips’ low-energy SMART Biphasic waveform, a highly effective defibrillation therapy that is also gentle to the heart. No other external defibrillation therapy has been supported by more published studies. Realistic training To help responders maintain their skills, Philips gives you a wide range of training solutions. When equipped with training pads and the rechargeable training and administration pack, you can use your FR2+ as a trainer. Its shock delivery capability is disabled while you train with ten scenarios. When you connect the FR2+ to a simulator or a special manikin that simulates an ECG rhythm, you can elicit realistic FR2+ responses to various heart rhythms for even more refined training. Philips also offers an economical AED trainer that comes with ten scenarios. An optional remote control enables instructors to pace the scenario to match their instruction, and to challenge the trainee with surprise scenario changes. Also available is the comprehensive AED Little Anne training system, featuring a manikin that gives the student feedback on pad placement. Comprehensive data management To maintain high standards of response timeliness and quality, many organizations place a high premium on detailed retrospective event reporting. The FR2+ facilitates this with an optional data card that captures up to 8 hours of patient heart rhythm, defibrillator use and, if configured, voice recording of the event. The removable data card lets you produce a variety of reports using the HeartStart Event Review suite of software products, without taking your FR2+ out of service. Built to perform and backed by Philips A five-year warranty and limited product indemnity comes with every HeartStart Defibrillator. Best of all, neither maintenance nor service contracts are required to maintain indemnification benefits. An extended two-year warranty is available. Coupled with the standard five-year warranty, the extended warranty gives you peace of mind, knowing your investment is protected for up to seven years. |
| Defibrillator | Patient Analysis System | ||
| Defibrillator Model | With ECG: M3860A With Text Only Display: M3861A |
Patient Analysis | Per protocol, evaluates patient ECG and signal quality to determine if rhythm is shockable, and evaluates connection impedance for proper defibrillation pad contact |
| How Supplied | Defibrillator, Instructions for use, standard battery, defibrillator pads (2 pair), quick reference | Sensitivity/ Specificity |
Meets AAMI DF-80 guidelines and AHA recommendations for adult defibrillation (Circulation 1997;95:1677-1682) |
| Waveform | Truncated exponential biphasic. Waveform parameters adjusted as a function of patient impedance | SMART CPR (configurable) |
Enable support of an automated or user-initiated CPR interval prior to defibrillation
The AUTO 1 and AUTO 2 settings automate the decision of whether to provide CPR first or deliver a shock first based on the amplitude and frequency of the presenting shockable rhythm. Once the decision is made, FR2+ provides the responder with the appropriate prompts. SMART AUTO 1: advises CPR for patients with a presenting rhythm typical of very long duration cardiac arrest SMART AUTO 2: advises CPR for an expanded group of patients inclusive of those in Auto 1, having a rhythm typical of long duration cardiac arrest USER: user initiated CPR Pause interval. Supports a protocol under which the responders decides whether to perform CPR first. A Pause-for-CPR button is enabled, and can be pressed at the responder's discretion |
| Energy | Single energy output. Adults: 150 J nominal into a 50 ohm load; Infant/Child: 50 J nominal into a 50 ohm load |
Quick Shock | Able to deliver a shock in typically less than 10 seconds after the end of a CPR interval |
| Charge Time from Shock Advised | Typically less than 10 seconds | HeartStart Adult Defibrillation Pads | |
| Charge Time in Manual Mode | Typically less than 5 seconds | Configuration | DP2: two pair or DP6: six pair |
| Shock-to-Shock Cycle Time | Typically less than 15 seconds (including analysis time) in automated mode | How Supplied | Disposable self adhesive pads with cable and connector |
| Protocol | Text and voice prompts guide user through protocol. Follows pre-configured settings. Can be modified with the M3864A training and administration pack | Surface Area | Meets AAMI DF-80 guidelines |
| Shock Delivery | Via defibrillator pads placed in anterior-anterior (lead II) position for adult defibrillation and anterior-posterior for infant/child defibrillation | Cable Length | Approximately 122 cm (48 inches) |
| Controls | On/Off, shock, screen contrast, option buttons | HeartStart FR2 Infant/Child Defibrillation Pads (M3870A) | |
| Indicators | LCD screen, beeper, audio speakers, status indicator, shock button, connector socket LED | Patient | Under 8 years or 25 kg (55 lbs.) |
| Advanced Mode | Configurable protocol | Defibrillator Compatibility | FR2-series (FR2 and FR2+) automated external defibrillator only |
| Physical | Configuration | M3870A FR2 Infant/Child reduced energy defibrillator pads. 1 set per package | |
| Size: Height Width Depth |
6.6 cm / 2.6 inches 21.8 cm / 8.6 inches 21.8 cm / 8.6 inches |
How Supplied | Disposable self adhesive pads with cable and connector |
| Weight With battery Without battery |
2.1 kg / 4.7 lbs 1.8 kg / 3.9 lbs |
Energy Delivered | Reduces defibrillator shock energy to nominal 50 Joules into a 50 ohm load |
| ECG Display (M3860A) | Surface Area | Meets AAMI DF-80 guidelines | |
| Screen | High resolution LCD with bright back light | Cable Length | Approximately 122 cm. (48 inches) |
| Screen Dimensions | 2.8 inches wide x 2.3 inches high (7 cm x 5.8 cm) | Medical Control / Recording Features | |
| Display Range | Differential: ± 2 mV full scale (nominal) | Standard Event Review | Elapsed time and number of shocks are displayed on screen |
| Sweep Speed | 23 mm / second (nominal) | Enhanced Event Review | Optional data card (M3854A) expands the above on-screen event review capabilities. Review chronological events in detail including ECG. 8 hours of event and ECG recording or one hour if voice recording is activated |
| Frequency Response | 1Hz to 20Hz (-3dB) (nominal) | ||
| Sensitivity | 1.16 cm/mV (nominal) | ||
| Heart Rate | 30 to 300 beats per minute updated each analysis period during monitoring | ||
| Monitored Lead | Anterior-anterior (lead II) placement with adult defibrillation pads or ECG Assessment Module (M3860A only) | ||
| FR2 Series Standard Battery | |
| Type | 12VDC 4.2 Ah lithium manganese. Disposable, recyclable, long-life, primary cells |
| Capacity | Minimum 300 shocks or 12 hours operating time |
| Install-by Date | Battery is labeled with an install-by date at least 5 years from date of manufacture |
| Standby Life | Defines how long the battery will power the AED in standby operation within the standby temperature range (one battery insert, test, no uses). 4 years minimum when battery is installed by the install-by date (5 years typical) |
| Environmental / Physical Requirements | |
| Sealing | Meets IEC529 class IP54 with battery and data card tray installed |
| Temperature | Operating: 0º - 50º C (32º - 122º F) Standby: 0º - 43º C (32º - 109º F) Standby applies to AED with battery installed and stored with defibrillation pads |
| Humidity | Operating: 0% to 95% relative humidity (non-condensing) Standby: 0% to 75% relative humidity (non-condensing) |
| Altitude | -500 to 15,000 feet per MIL-STD-810E 500.3 Procedure II |
| Aircraft | Method: RTCA/D0-160D: 1997 Section 21 (Category M - Charging) |
| Shock / Drop Abuse Tolerance | 1 meter any edge, corner or surface. MIL-STD 810E 516.4 Procedure IV |
| Vibration | MIL-STD 810E 514.4-17 |
| EMI | Requirements: Tested to EN60601-1-2 Limits Radiated: Method EN55011: 1998 Group 1 Level B Immunity: Method EN61000-4-3:1998 Level 2 |
| Automated and User Activated Self-Tests | |
| Automatic Self Tests | Tests internal circuitry, waveform delivery system and battery capacity. Verifies calibration of key circuits monthly |
| Automatic Self Test Frequency | Daily when stored withing operating environmental conditions |
| Satus Indication | Dynamic visual and audible indication of self test results. Indicates device readiness |
| Battery Insertion Test | Upon battery insertion, extensive automatic self tests and user interactive tests check device readiness. Verifies calibration of key circuits |
| Automatic Standby Temperature Monitoring | Instrument automatically monitors temperatures and warns user if device is stored outside of standby temperature range |
| FR2+ Training and Administration Pack (M3864A) | |
| Function | Places FR2+ in scenario-based training mode and disables energy delivery. 10 real world scripts provided. Permits modification of preprogrammed FR2+ protocol |
| Type | 12 VDC 1.1 AH Rechargeable Nickel Metal Hydride |
| Capacity | Minimum 4 hours training time |
| Recharge Time | 90 minutes to full capacity using M3855A charger (sold separately) |
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