Data Sheet
Technical Overview
SAM
500P
Physical
With Pad-Pak
™
Inserted
Size: 20 cm x 18.4 cm x 4.8 cm (8.0 in x 7.25 in x 1.9 in)
Weight: 1.1 kg (2.4 lbs)
Debrillator
Waveform:
Self-Compensating Output Pulse Envelope (SCOPE
™
)
0ptimised biphasic escalating waveform compensates
energy, slope and duration for patient impedance
Warranty: 8-year limited warranty
Patient Analysis System
Method:
Evaluates patient’s ECG, signal quality, electrode
contact integrity and patient impedance to
determine if debrillation is required
Sensitivity/Specicity: Meets IEC/EN 60601-2-4
Impedance Range: 20 - 230 ohms
Environmental
Operating/Standby
Temperature:
0°C to 50°C (32°F to 122°F)
Transportation
Temperature:
–10°C to 50°C (14°F to 122°F) for up to two days.
If the device has been stored below 0°C (32°F), it should
be returned to an ambient temperature of between
0°C to 50°C (32°F to 122°F) for at least 24 hours
before use.
Relative Humidity: 5% to 95% (non-condensing)
Enclosure: IEC/EN 60529 IP56
Altitude: 0 to 4 575 metres (0 to 15 000 feet)
Shock: MIL STD 810F Method 516.5, Procedure 1 (40 G’s)
Vibration:
MIL STD 810F Method 514.5+, Procedure 1
Category 4 Truck Transportation – US Highways
Category 7 Aircra – Jet 737 & General Aviation
EMC: IEC/EN 60601-1-2
Radiated Emissions: IEC/EN 55011
Electrostatic Discharge: IEC/EN 61000-4-2 (8 kV)
RF Immunity:
IEC/EN 61000-4-3 80 MHZ-2.5 GHZ, (10 V/m)
Magnetic Field Immunity: IEC/EN 61000-4-8 (3 A/m)
Aircra:
RTCA/DO-160G, Section 21 (Category M)
RTCA/DO-227 (ETSO-C142a)
Falling Height: 1 metre (3.3 feet)
Energy Selection
Pad-Pak: Shock 1: 150J; Shock 2: 150J; Shock 3: 200J
Paediatric-Pak: Shock 1: 50J; Shock 2: 50J; Shock 3: 50J
Charging Time
New Battery: Typically 150J in < 8 seconds, 200J in < 12 seconds
Event Recording
Type: Internal Memory
Memory:
90 minutes of ECG (full disclosure) and event/
incident recording
Review:
Custom USB data cable (optional) directly connected
to PC with Saver EVO
™
Windows-based data review
soware
Materials Used
Housing: ABS, Santoprene
Electrodes: Hydrogel, Silver, Aluminum and Polyester
Pad-Pak — Electrode and Battery Cartridge
Adult Pad-Pak (Pad-Pak-03) and Paediatric Pad-Pak (Pad-Pak-04)
*ETSO- certied aviation Pad-Pak also available
Shelf Life/Standby Life:
See the expiration date on the Pad-Pak/Paediatric-Pak
(4 years from manufacture date)
Weight: 0.2 kg (0.44 lbs)
Size: 10 cm x 13.3 cm x 2.4 cm (3.93 in x 5.24 in x .94 in)
Battery Type:
Disposable single-use combined battery and debrillation
electrode cartridge (lithium manganese dioxide
(LiMnO2) 18V)
Battery Capacity (New):
> 60 shocks at 200J or 6 hours of continuous
monitoring
Electrodes:
HeartSine samaritan disposable debrillation pads
are supplied as standard with each device
Electrode Placement:
Anterior-lateral (Adult);
Anterior-posterior or Anterior-lateral (Paediatric)
Electrode Active Area:
100 cm
2
(15 in
2
)
Electrode Cable Length: 1 metre (3.3 feet)
Aircra Safety Test
(ETSO-certied
Pad-Pak):
RTCA/DO-227 (ETSO-C142a)
1. Valenzuela TD, et al. 2000. Outcomes of Rapid Debrillation by Security Ocers Aer Cardiac Arrest in Casinos. New England Journal of Medicine. 343:1206-09.
2. Mosesso Jr VN, et al. 2002. Proceedings of the National Center for Early Debrillation Police AED Issues Forum. Prehospital Emergency Care. 6(3):273–82.
3. Walsh SJ, McClelland A, Owens CG, Allen J, McCanderson J, Turner C, Adgey J. Ecacy of distinct energy delivery protocols comparing two biphasic debrillators for cardiac arrest.
Am J Cardiol. 2004;94:378–380.
EMEA/APAC
HeartSine Technologies, Ltd.
203 Airport Road West
Belfast, Northern Ireland
BT3 9ED
Tel: +44 28 9093 9400
Fax: +44 28 9093 9401
U.S./Americas
HeartSine Technologies LLC
121 Friends Lane, Suite 400
Newtown, PA 18940
Toll Free: (866) 478 7463
Tel: +1 215 860 8100
Fax: +1 215 860 8192
The SAM 500P is not available for sale in the U.S.
© 2018 HeartSine Technologies LLC. All rights reserved.
For further information contact us at heartsinesupport@stryker.com or visit our website at www.heartsine.com.
The HeartSine products
described in this brochure
meet the European Medical
Directive requirement.
UL Classied. See complete
marking on product.
H009-014-025-3 Intl