Philips Heartstart FR3 Defibrillator with Battery & Hard Case

Condition: Used
This item has been previously used and may show signs of cosmetic wear. However, it is in full operational condition and functions as intended. It could be a floor model or a store return. Please refer to the listing for comprehensive details and descriptions of any imperfections.

Important Note:

• We do not have the facilities to calibrate our equipment.
• We do not service medical items.

We strongly recommend that you have the item professionally serviced, calibrated, and cleaned before use.

The Philips Heartstart FR3 Defibrillator is specifically designed to be used efficiently during emergency situations. Its SMART Pads III have a convenient peel-and-place design that is suitable for both adults and children. With its compact size and lightweight construction, it can easily be moved around, even in tight or crowded spaces. The Quick Shock feature ensures rapid treatment by minimizing the time between shock delivery. In addition, the 3-Lead ECG cable provides critical information for accurate assessment and decision-making in non-cardiac arrest cases. Philips offers various data management solutions to assist in continuous improvement and excellence in patient care. The FR3 is built tough and versatile, meeting rigorous military standards through extensive testing. Its IP55 rating protects against dust and water jets, and it can withstand a 1,100-pound crush test. The FR3 allows for customisation to fit current and future protocols, making it highly adaptable.

The Hard case for FR3 is designed with room for a spare battery, spare AED pads and infant/child key. The Philips HeartStart FR3 status indicator can be seen through the clear window without having to remove the AED from the carrying case.

Expertly designed, the Philips HeartStart FR3 Defibrillator with Battery & Hard Case has a spacious interior for storing a spare battery, spare AED pads, and an infant/child key. Thanks to the clear window, you can easily monitor the device's status without even having to remove it from the protective carrying case - making it easy to access and transport in emergency situations.

What's included:

• 1X FR3 Defibrillator
• 1X Child Key
• 1X Pads (expired)
• 1X battery (please select year)
• 1X Hard case

Specifications

Screen	Screen LCD color display, 320 x 240 pixels 2.8˝ x 2.1˝ (7.2 cm x 5.4 cm)
Bandwidth	Bandwidth 1 Hz to 30 Hz (-3dB), nominal (non-diagnostic)
Monitored Lead	Monitored lead Lead II using anterior-anterior adult pads placement

Environment/physical

Shock/drop	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
Temperature	Operating/standby: 32°–122°F (0°– 50°C)
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

Patient analysis system

ECG analysis	Evaluates impedance of pads for contact, ECG rhythm and signal quality
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 defib
SMART CPR	Evaluates key characteristics of presenting VF and determines initial therapy.

FR3 primary battery

Type	Type 12 VDC, 4.7 Ah, lithium manganese dioxide Long-life primary cells
Capacity	Please consult User’s Manual for capacity specifications.
Standby life	3 years minimum when stored under standby environmental conditions
Shelf life	5 years

SMART Pads III

Application	Peel and place pads can be removed from packaging and stored in carry case.

Infant/Child Key

Function	Selects therapy for infants or children under 55 lbs (25 kg) or 8 years old

FR3 data card

Function	Function Stores a minimum of 8 hours of ECG, event, and voice recording.

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

Defibrillator

Models	Models 861388 text display 861389 ECG and text display
Waveform	SMART Biphasic Truncated Exponential waveform parameters adjust as a function of patient impedance.
Shock delivery	Via defibrillator pads placed in the anterior-anterior position for adults, infants and children.
Indicators	High-res LCD, beeper, voice prompts, tones, speaker, connector socket
Advanced mode	Advanced mode Configurable using optional HeartStart Configure software

Environmental/Physical Requirements

Sealing	Meets IEC529 class IP55 with battery installed
Operating Temperature	Operating/standby: 32°–122°F (0°– 50°C)
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)
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)
Vibration	Meets MIL-STD-810F 514.5 C-17

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

Please read our terms and conditions carefully before using any medical device purchased from SelfiMed.

Potential Risks

New, used, replaced, or repaired medical devices can be dangerous. They may cause serious injury or death to the user or patient.

SelfiMed is not authorized to give medical advice or operate medical devices. We do not provide service or repairs for medical devices. Do not buy used medical equipment if you have a health emergency or a seriously ill relative unless advised by an expert.

Required Checks and Maintenance

All medical devices sold by SelfiMed come from NHS hospitals but with an unknown service history. Therefore, they may require maintenance and thorough health and safety checks before use.

These checks must be carried out by a qualified professional to ensure patient and user safety.

Liability Disclaimer

SelfiMed assumes no liability for the misuse or improper use of medical devices, including incidents that result in severe injury or death.

Regulatory Compliance

Our products are NHS-approved and therefore comply with the essential requirements of the UK Medical Devices Regulations and the EU Council Directive 93/42/EEC, as amended by Directive 2007/47/EC, and are classified as Class IIa devices.

The sale of this item may be subject to regulation by UK, EU, and FDA regulatory agencies. You must be an authorized purchaser to bid on this item.

Consult a Qualified Professional

The members of the SelfiMed UK store are not qualified to give medical advice on any medical equipment. For any questions related to the use of medical devices, please consult your General Practitioner (GP), physician, nurse, or medical technologist.

For further inquiries, contact SelfiMed at info@selfimed.com or +44 780 2644 820.