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LIFEPAK® 10

defibrillator/monitor/pacemaker

Rugged, transport unit

User-friendly controls and display

Optional built-in noninvasive pacing

AC or DC auxiliary power supply

Serial 12-lead adapter available

Optional “hands-free” defibrillation adapter

CODE SUMMARYâ„¢ critical event record

The Medtronic Physio-Control LIFEPAK 10 defibril- lator/monitor/pacemaker was designed to with- stand the harsh environment faced by emergency medical providers throughout the world. This rugged, portable unit, which follows the tradition of the company’s LIFEPAK 5 defibrillator/monitor, is built tough to withstand demanding field requirements.

Features include simple 1-2-3 operation and user- friendly display, and CODE SUMMARY critical event record, which recaps critical events from the moment of “power on.” This unit also features optional built-in noninvasive pacing, AC or DC auxiliary power supply, and a defibrillation adapter for “hands-free” defibrillation. A serial 12-lead adapter is also available.

For ease in transferring a patient from prehospital to hospital care, electrodes and cables are compat- ible with the family of LIFEPAK 9 defibrillator/ monitors. This unit was designed for easier maintenance with on-screen diagnostics for test and calibration. It also includes an integral chassis which allows 360° serviceability.

The LIFEPAK 10 defibrillator/monitor/pacemaker joins the Medtronic Physio-Control family of pre- hospital products.

SPECIFICATIONS I LIFEPAK 10 defibrillator/monitor/pacemaker

ECG MONITOR

ECG lead selection: Paddles I, II, III

Input: Isolated ECG via QUIK-LOOK® defibrillator paddles, FAST-PATCH® electrodes, or 3-lead patient cable.

ECG cable length: 3.96m (13 ft) total length; 3.05m cable (10 ft); with .91m leads (3 ft)

Electrical isolation and shielding: Input protected against high voltage defibrillator pulses and radio frequency interference per FDA Standard MDS-201-0004. RF inter- ference depends on distance from RF source, radio output power, radiating frequency, vehicle environment, etc.

Common mode rejection: Minimum 100dB with respect to chassis ground at 60Hz, 65dB minimum with respect to isolated ground.

Cardioscope display

Size: 72.5mm (2.85 in) x 43.5mm (1.7 in), non-fade

Sweep speed: 25mm/sec

Frequency Response:

1 to 30Hz, -3dB (monitor freq. resp.—domestic)

0.5 to 25Hz, -1.4dB (monitor freq. resp.—agency)

0.05 to 30Hz, -3dB (expanded freq. resp. while recorder in DIAG mode)

2 to 20Hz, -3dB (paddles freq. resp.)

Strip chart recorder

Paper size: 50mm x 30m (100 ft)

Paper speed: 25mm/sec

Frequency Response:

1 to 30Hz, -3dB (monitor freq. resp.—domestic)

0.5 to (-1.4dB) to 40 (-3dB) Hz, (monitor freq. resp.— agency)

0.05 to 100Hz, -3dB (diagnostic freq. resp.)

2 to 20Hz, -3dB (paddles freq. resp.)

1 to 30Hz (CODE SUMMARY—domestic)

0.5 to 40Hz (CODE SUMMARY—agency)

Annotation: Includes time, date, lead, gain, heart rate, defibrillator and/or pacing parameters.

CODE SUMMARY critical event record: Digitally stored record of critical ECG and device parameters.

Status display:

•Heart rate: 3 digit readout displays rates from 20 to 295 bpm

•Available energy

•Pacing rate (optional)

•Pacing current (optional)

•DIAG (if recorder is operating in diagnostic frequency)

ECG output:

•Unmodulated: 1V/mV at x 1.0 gain

•Modulated: 1400Hz ± 2% center frequency, 1Vrms, ± 10%

•Frequency response: matches strip chart recorder

QUIK-PACE® NONINVASIVE PACEMAKER

Output rate: 40 to 170 bpm

Output waveform: Monophasic, truncated, exponential current pulse (20msec; 15 to 25% droop)

Output current: 0 to 200mA

Refractory period: 200 to 340msec (function of rate)

DEFIBRILLATOR

Waveform: 5msec monophasic pulse (Edmark) per AAMI spec

Energy select: 0, 5, 10, 20, 50, 100, 200, 300, 360J

Paddle controls: Charge (with indicator light); Record (activates strip chart recorder); Energy select (rotating dial; 0 to 360J); Discharge (dual energy discharge buttons, one on each paddle).

Charge time: Charge to 360 joules in less than 12 seconds above 0°C.

Paddle area: 82cm2

Synchronizer: Delivers energy discharge within 20msec of sync marker on cardioscope (triggers to patient generated QRS complex).

Cord length: 2.3m (7.5 ft)

ENVIRONMENTAL

Temperature:

Standby: 5 to 55°C (41 to 131°F)

Operating: -10 to 55°C (14 to 131°F) after minimum two hour storage at standby temperature

Storage (exclusive of batteries): -30 to 65°C (-22 to 149°F)

Humidity:

0 to 95% (noncondensing)

0to 34°C (32 to 93.2°F)

0to 80% (noncondensing) 35 to 55°C (95 to 131°F)

Atmospheric pressure: 797 to 439mmHg (-570 to +15,000 ft)

Shock (Drop): With carrying case (soft case), passes drops of 43 inches from the handle (30 inches from case). This exceeds test levels per ECRI Report, Contract No. 223-77-5035, prepared for FDA (April 1979).

Vibration Helicopter Aircraft: MIL-STD-810D, Method 514.3 (category 6). Test levels per U.S. Army Aeromedical Research Laboratory Report No. 91-14, Section 2.6.3. (March 1991), (UH-1 helicopter, floor under co-pilot's seat).

Vibration Fixed-Wing, Turboprop Transport: (take off and climb) Test level of .0016g2/Hz, the maximum level per figure 32(31) of ECRI Report, Contract No. 223-77-5035. Prepared for FDA (April 1979).

Sealed case: MIL-STD-108E and IEC 601-2-4

GENERAL

Battery: 3 NiCad batteries, 12V, 1.0 amp hours each.

A new Battery Pak registering at least 100% capacity on the Battery Support System will provide at a minimum:

•45 minutes of monitoring or

•30 minutes of pacing or

•25 discharges at 360 joules per Battery Pak

Physical characteristics

Height: 10.4cm (4 in)

Width: 40.6cm (16 in)

Depth: 37cm (14.6 in)

Weight: 9kg (20 lbs)

All specifications at 25°C unless otherwise stated.

 

Medtronic Physio-Control

United Kingdom, Ireland

Italy

Asia Pacific

Poland

 

11811 Willows Road NE

Basingstoke, Great Britain

Sesto Fiorentino, Italy

Christchurch, New Zealand

Warsaw, Poland

 

P. O. Box 97006

Tel: 44.1256.782.727

Tel: 39.055.302.701

Tel: 64.3.3794.429

Tel: 48.22.613.38.13

 

Redmond, WA 98073-9706 USA

Fax: 44.1256.782.728

Fax: 39.055.302.4029

Fax: 64.3.3792.374

Fax: 48.22.613.38.11

 

Tel: 425.867.4000

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Fax: 425.867.4121

 

Lyon - St Priest, France

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Miami, Florida

Prague, Czech Republic

 

Internet: www.physiocontrol.com

 

Internet: www.medtronic.com

Tel: 33.4.72.79.26.26

Tel: 31.20.6.533.640

Tel: 786.242.6661

Tel: 420.2.2017.2277

 

Europe

Fax: 33.4.72.79.26.36

Fax: 31.20.6.535.822

Fax: 786.242.4505

Fax: 420.2.2056.1617

 

Germany, Switzerland

Spain

Middle East

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Basingstoke, Great Britain

 

Fernwald, Germany

Madrid, Spain

Dubai, UAE

of China

 

Tel: 44.1256.782.727

 

Fax: 44.1256.782.728

Tel: 49.6404.91.41.0

Tel: 34.91.375.6050

Tel: 971.4.282.6532

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Fax: 49.6404.91.41.20

Fax: 34.91.375.6055

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Tel: 86.10.6708.1162

 

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Fax: 86.10.6708.1163

 

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Tel: 905.709.4330

 

 

Tel: 43.1.240.44.160

Tel: 46.8.580.945.00

Tel: 36.1.214.2228

 

 

Fax: 905.709.3336

 

 

Fax: 43.1.240.44.600

Fax: 46.8.580.945.05

Fax: 36.1.214.2230

 

 

 

 

LIFEPAK, FAST-PATCH, QUIK-PACE and QUIK-LOOK are registered trademarks of Medtronic Physio-Control Corp. CODE SUMMARY is a trademark of Medtronic Physio-Control Corp. Medtronic is a registered trademark of Metronic, Inc. Specifications subject to change without notice. ©1999 Medtronic Physio-Control Corp. Litho in USA.

P/N 805132-001