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The Philips HeartStart FR2 is a portable, lightweight automated external defibrillator (AED) that requires minimal device training to use and is an essential part of administering first aid immediately to a victim of sudden cardiac arrest. Due to its easy-to-use design, superior technology and affordability, FR2 AEDs are now being placed in a wide range of settings such as hospitals and clinics, offices and industrial locations, airports and airplanes, health clubs and golf courses. This innovative AED technology has also enabled a broader range of people beyond community EMS professionals to provide lifesaving therapy.
The FR2 AED operates with long-life maintenance-free, lithium manganese batteries, which are designed specifically for high-volume consumer applications, where safety and reliability are of the utmost importance. The FR2 performs daily automated self-tests that check readiness for use. Other features include easy-to-follow voice prompts, and a bright LCD display to reinforce the voice prompts, making it easy to use in noisy or dark settings; the FR2 also has enhanced features that can be enabled for improved hand-off to advanced life support (ALS) responders. Additionally, the FR2 has on-board training capabilities when used with the fully rechargeable Training and Administration Pack. This allows users to safely train on the FR2 using realistic training scenarios.
The FR2 AED incorporates a number of breakthrough technologies that distinguish it from other AEDs on the market, including the low-energy SMART Biphasic technology. Additionally, the SMART Analysis system automatically determines if a shock is required and protects against inappropriate delivery of a shock. This feature eliminates the need for the operator to be trained in reading and interpreting the patient's electrocardiogram (ECG).
The 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 life-saving therapy. Commands are clear, streamlined, confident, and concise: ideal for responders who are trained, drilled, and ready to save a life now.
The HeartStart FR2+ offers features that make hand-off to ALS professionals seamless for maximum continuity of care for the patient.
An ECG display is available. 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, refinement by 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 save a life with the FR2+.
Optimized for Challenging Environments
Because of its ruggedness and ability to stand up to temperature extremes and wet conditions, 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 light-weight so it won't weigh you down.
Versatile - The FR2+ is designed to be highly flexible and versatile. You can tailor your FR2+ to match your specific response protocol.
Infant/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, 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 light-weight defibrillator/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 HeartStart 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+ is ready for use.
The Most Thoroughly Proven Therapy - The FR2+ uses the proven SMART Analysis algorithm to ensure that a shock is delivered only if it is appropriate. And Philips low-energy SMART Biphasic waveform delivers a highly effective defibrillation shock that is also gentle to the heart. No other external defibrillation therapy has been supported by more clinical data.
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 records patient heart rhythm, defibrillator use and, if configured, voice recording of the event. The removable data card lets you produce a variety of reports via Coderunner PC software, without taking your FR2+ out of service.
Heartstream FR2 AED Features:
- Daily automated self-tests check FR2's readiness
- Clear, concise, easy-to-follow voice prompts guide the caregivers
- Text messages shown on the bright LCD display reinforce voice prompts
- On-board training capabilities allows users to safely train on the FR2 using realistic training scenarios
- Long-life maintenance-free, lithium manganese batteries
Benefits
- Innovative technology enables a broad range of people - beyond community EMS professionals - to provide lifesaving therapy
- SMART Analysis system automatically determines if a shock is required and protects against inappropriate shock delivery
- Patented low-energy, SMART Biphasic waveform is clinically proven superior to high-energy, monophasic waveforms for efficacy and for minimizing post-defibrillation heart dysfunction
- Easy to use, even in noisy or dark settings
Specifications:
| Defibrillator Model |
With ECG M3860A.
With Text Only Display M3861A. |
| How Supplied |
Defibrillator, instructions for use, standard battery, defibrillator pads (2 pair), quick reference card. |
| Waveform |
Truncated exponential biphasic. Waveform parameters adjusted as a function of patient impedance. |
| Energy |
Single energy output.
Adults:150 J nominal into a 50 ohm load.
Pediatric: 50 J nominal into a 50 ohm load. |
| Charge Time From Shock Advised |
Typically less than 10 seconds. |
| Shock-to-Shock Cycle Time |
Typically less than 20 seconds (including analysis time) in automated mode. |
| Protocol |
Text and voice prompts guide user through protocol. Follows pre-configured settings. Can be modified with the M3864A training & administration pack. |
| Shock Delivery |
Via defibrillator pads placed in anterior-anterior (lead II) position for adult defibrillation and anterior-posterior for infant/child defibrillation. |
| Controls |
On/off, shock, screen contrast/option buttons. |
| Indicators |
LCD screen, beeper, audio speakers, status indicator, shock button, connector socket LED. |
| Advanced Mode |
Configurable protocol. |
Size
� � Height
� � Width
� � Depth
|
�
6.6 cm. (2.6 inches).
21.8 cm. (8.6 inches).
21.8 cm. (8.6 inches).
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Weight
� � With battery
� � Without battery |
�
2.1 kg. (4.7 pounds).
1.8 kg. (3.9 pounds). |
| Screen |
High-resolution LCD with bright back light. |
| Screen Dimensions |
2.8 inches wide x 2.3 inches high (7.0 cm x 5.8 cm). |
| Display Range |
Differential: �2 mV full scale (nominal). |
| Sweep Speed |
23 mm/second (nominal). |
| Frequency Response |
1 Hz to 20 Hz (-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). |
| Patient Analysis |
Per protocol, evaluates patient ECG and signal quality to determine if a shock is appropriate, and evaluates connection impedance for proper defibrillation pad contact. |
| Sensitivity/Specificity |
Meets AAMI DF-39 guidelines. |
| Type |
12 VDC 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 and no uses). 4 years minimum when battery is installed by the Install-By-Date (5 years typical). |
| Configuration |
DP2: two pair or DP6: six pair. |
| How Supplied |
Disposable self-adhesive defibrillation pads with integrated cable and connector. |
| Surface Area |
100 cm2 each (nominal active surface area). |
| Cable Length |
Approximately 122 cm (48 inches). |
| Patient |
Under 8 years or 25 kg (55 pounds). |
| Defibrillator Compatibility |
FR2-series (FR2 and FR2+) automated external defibrillator only. |
| Configuration |
M3870A FR2 Infant/Child Reduced Energy Defibrillator Pads. 1 set per package. |
| How Supplied |
Disposable self-adhesive pads with cable and connector. |
| Energy Delivered |
Reduces defibrillator shock energy to nominal 50 Joules into a 50 ohm load. |
| Surface Area |
44 cm2 each pad (nominal active surface area). |
| Cable Length |
Approximately 122 cm (48 inches). |
| Standard Event Review |
Elapsed time and number of shocks are displayed on screen. |
| 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 & ECG recording or one hour if voice recording is activated. |
| Sealing |
Meets IEC529 class IP54 with battery and data card tray installed. |
| Temperature |
Operating: 0� - 50� C (32� - 122� F). Standby: 0� - 43� C (50� - 109� 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/DO-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. |
| 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 within operating environmental conditions. |
| Status 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 inter-active tests check device readiness. Verifies calibration of key circuits. |
| Automatic Standby Temperature Monitoring |
Instrument automatically monitors temperature and warns user if device is stored outside of standby temperature range. |
| 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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