Rescue SAM 4.0’s smart connection system recognises the plates and sets the shock to the most appropriate protocol for the adult or paediatric patient.The special connector has been made to ensure the best construction standards.

Rescue Sam 4.0D was designed to also be used in the most extreme emergencies. It was therefore subjected to countless tests by accredited, avant-garde laboratories, who worked to ensure that our devices are durable, sustainable and safe and that they can withstand shocks, impacts and the entry of dust and liquids (IP55).

TECHNICAL SPECIFICATIONS:

DEFIBRILLATOR

How to use: semi-automatic, for adult and paediatric use.

Waveform: Biphasic Truncated Exponential (BTE) controlled by impedance measurement.

Energy:

adults: ±xed at 200J – paediatric: less than 50J Charging time from discharge warning: <8 seconds to 200J with new battery; <5 seconds at 50J on paediatric patients.

Pacemaker detection: detection and removal of the artefact created by the pacemaker

DISPLAY

Type: 7’’ colour LCD, resolution 800×480 pixels Brightness control: 10 settable levels

ECG

Band: ECG displayed: 0.25 – 160 Hz

CMRR: 120 dB

Input impedance: ›500MΩ

Amplitude: 25 mm/mV

Speed: 37.5 mm/s

Filters: ±xed ±lters for removing supply disturbances, baseline wandering and signal conditioning

HR frequency range: 20 – 300 bpm

PHYSICAL & ENVIRONMENTAL

Dimensions: 250 x 260 x 80 mm

Weight: 2.2 kg including battery and standard accessories

Protection class: IP 55

Operating temperature: -20°- 60 °C

BATTERY

Characteristics: 12V DC, 4200mAh non-chargeable long-lasting lithium-manganese battery, internal memory.

Capacity: up to 12 hours in continuous operation or up to 200 shocks at maximum energy 200 J

AUTOMATIC SELF-TEST

Battery insertion test, Daily, Weekly, Monthly Tests, Battery check

DATA RECORDING AND TRANSFER

Internal memory: up to 16 hours recording ECG tracing and events

Environmental recording: ›2 hours (optional)

CONNECTIVITY

USB: standard, micro-B

STANDARDS AND SAFETY

IEC standard: EN 60601-1; EN 60601-1-1;

EN 60601-1-2; EN 60601-2-4

EC mark: EEC 93/42, medical device