M Series
CCT
M Series CCT Specifications
Defibrillator
Waveform: ZOLL Rectilinear Biphasic.
Energy Selection: Selectable at 1, 2, 3, 4, 5, 6, 7, 8, 9, 10,
15, 20, 30, 50, 75, 100, 120, 150, 200 joules. (Delivered
into 50 ohm load.)
Charge Time: Less than 6 seconds with a new fully charged
battery (first 15 charges to 200J.) Depleted batteries will
result in a longer defibrillator charge time.
Energy Display: Monitor display indicates both selected and
delivered energy.
Synchronized Mode: Synchronizes defibrillator pulse to
patient’s R-wave. "SYNC" message displayed on monitor.
Marker on display and recorder paper identifies R-wave
discharge point.
Advisory Function: Single analysis or programmable auto
re-analyze x3 with programmable auto energy level
selection, screen prompts, and voice prompts.
Charge Controls: Control on apex paddle and on device
front panel.
Paddles: External anterior/anterior adult and pediatric.
Adult paddles slide off to expose pediatric paddles.
Multi-Function Electrode (MFE) Pads: Specifically designed
adult anterior/posterior pre-gelled ZOLL MFE Pads, and
Multi-Function stat • padz™ packaged in pairs.
Built-In Defibrillator Tester: Tests defibrillator energy
output and continuity of universal cable and paddles;
documented on PCMCIA card and strip chart.
Defibrillation Advisory: Evaluates electrode connection and
patient ECG to determine if defibrillation is required.
Shockable Rhythms: Ventricular fibrillation with amplitude
> 100 µV and wide complex ventricular tachycardia with
rates greater than 150 bpm.
Multi-Function Electrode Impedance Measurement
Range: 0-250 ohms.
Display
Screen Type: Color LCD.
Screen Size: 6.5 inches (16.5 cm) diagonally.
Sweep Speed: 25 mm/sec.
Viewing Time: 4 seconds.
Traces: 3.
Information: Heart Rate, Lead/Pads, Alarm On/Off,
Advisory Functions and Prompts, Defibrillator Test
Function, Error Corrections and Faults, Code Markers,
Alarm Selection and Limits, Delivered Energy, SpO2 ,
Pacer Functions, EtCO2 , NIBP, Invasive Pressures (2),
Temperature (2).
ECG Monitoring
Patient Connection: 3-lead ECG cable, 5-lead ECG cable,
12 lead cable, paddles or MFE Pads. Input selection on
front panel.
Input Protection: Fully defibrillator protected. Special
circuit prevents distortion of ECG by pacer pulse.
(Pacer version only.)
Implanted Pacemaker Spike Display: Dedicated circuitry
detects most implanted pacemaker spikes and provides
standard display marker of spike on ECG trace.
Bandwidth: 0.5-40 Hz (-3 dB) standard/0.05-150 Hz
diagnostic.
Lead Selection: Displayed on monitor.
ECG Size: 0.5, 1, 1.5, 2, 3 cm/mV - display on monitor.
Heart Rate: Digital display 0-300 bpm ±5%.
Heart Rate Alarm: On/Off displayed on monitor.
User-selectable, tachycardia 60-280 bpm, bradycardia
20-100 bpm.
1 Volt ECG Out: 1.0 volt/cm of deflection on strip chart
recorder. < 25 ms delay from patient ECG input.
Display Format: Non-fade moving bar display.
SmartAlarms™: Beeper/voice prompts indicate shockable
rhythm.
Recorder
Paper: 90 mm (width).
Speed: 25 mm/sec., 6-second delay.
Annotations: Time, date, defib energy, heart rate, pacer
output (pacer version only), QRS sync marker, ECG size,
lead, alarm, defib test OK/Fail, analyze ECG, analysis
halted, noisy ECG, shock advised, no shock advised,
ECG too large, ECG too small, and diagnostic bandwidth.
Printing Method: High-resolution, thermal array print head.
Printout Modes: Manual or automatic - user-configurable.
On/Off Control: Front panel and paddle.
Automatic Function: 15-second recording initiated by alarm activation or defibrillator discharge.
PCMCIA Card Slots
Accepts two standard series Type II Flash Cards, 1-16 MB:
Fax modem card capability in slot 2.
PCMCIA Card
Continuous recording of ECG, vital sign and device data;
episodic recording of NIBP data. Playback on PC equipped
with ZOLL Data Control and specified PCMCIA Card reader.
Battery Packs
Type: Rechargeable, sealed lead acid.
Recharge Time: 7.2 hours or less with integral charger.
Operating Time: For a new, fully charged battery pack at
20°C: 60 defibrillator discharges at maximum energy (200
joules); 2.5 hours continuous ECG and SpO2 monitoring;
2.3 hours of continuous ECG with pacing (60 mA at 80
bpm) and SpO2 monitoring, or 1.5 hours of continuous
ECG with pacing (60 mA at 80 bpm) SpO2 monitoring,
EtCO2 , and IBP monitoring.
Pulse Oximetry
Saturation (% SpO2 ) Range: 1%-100%.
Pulse Rate (bpm) Range: 25-240.
Saturation (% SpO2 ) Accuracy During No Motion
Conditions:
Adults - 70%-100% ± 2 digits, 0%-69% unspecified.
Saturation (% SpO2 ) Accuracy During Motion Conditions:
Adults - 70%-100% ± 3 digits, 0%-69% unspecified.
Pulse (bpm) Accuracy During No Motion Conditions: 25 to
240 ± 3 digits.
Pulse (bpm) Accuracy During Motion Conditions: 25 to 240
± 5 digits.
Saturation (% SpO2 ) Resolution: 1%.
Pulse Rate (bpm) Resolution: 1 BPM.
Bio-Compatibility: Patient contacting material meets
requirements
of ISO 10993-1, Biological Evaluation of Medical
Device — Part 1, for external devices, intact surfaces and
short-term exposure.
Note: The M Series Pulse Oximetry Option is calibrated
for functional saturation.
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Pacemaker (Option)
Type : VVI demand; asynchronous (fixed rate) when usedwithout ECG leads or in ASYNC pacing mode.
Pulse: Rectilinear, constant current; 40 milliseconds ±2ms;
amplitude variable 0 to 140 mA ±5% or 5 mA, whichever
is greater; digitally displayed on the monitor (increments
or decrements by a value of 2 mA); rate variable from 30
to 180 ppm ±1.5% (increments or decrements by a value
of 2 ppm).
Output Protection: Fully defibrillator protected and isolated.
Multi-Function Electrode (MFE) Pads: Specifically designed
pre-gelled ZOLL stat • padz
TM, pro-padz TMand pedi-padz TM MFE packaged in pairs.
EtCO2 (Option)
Sensor Type: Infrared, Mainstream.
Warm-Up Time: Operational in 15 seconds,
full specification within 60 seconds.
Step Response Time: Less than 60 ms adult, less than
50 ms neonate.
End Tidal CO2 (EtCO2 ) Range: 0-100 mmHg.
End Tidal CO2 (EtCO2 ) Accuracy: 0-40 mmHg ±2 mmHg,
41-70 mmHg ±-5%, 71-100 mmHg ±8%.
End Tidal CO2 (EtCO2 ) Resolution: 1 mmHg.
Respiration Rate (RR) Range: 0-150 respirations per minute.
Respiration Rate (RR) Resolution: 1 respiration/min.
EtCO 2 Alarm Limits: User-selectable/High 5 to 100 mmHg,
Low 0 to 95 mmHg/OFF.
Respiration Rate (RR) Alarm Limits: User-selectable, High
5 to 150 respirations per minute, Low 0 to100 respirations
per minute/OFF.
O2 /N2 O Compensation: User-configurable.
Halogenated Agents: Specification allows for halogenated
anesthetic agents, which may be present at normal clinical
levels. The presence of desflurane in the exhaled breath
beyond normal values (5-6%) may positively bias Carbon
Dioxide values by up to an additional 2-3 mmHg.
Barometric Pressure Compensation Range: 550-780 mmHg
(automatic).
Airway Adapter Deadspace: Adult <5 cc, Neonatal <.5 cc.
Environmental:
Operating Temperature: 10° to 40°C.
Storage and Shipping Temperature: -10°to 55°C.
Electromagnetic Immunity: (EtCO2 Option): AAMI DF-2:
IEC 1000-4-3, 15 V/m.
NIBP (Option)
Characteristics and Specifications
Patient Population: Adult, Pediatric.
Method: Oscillometric.
Control: Automatic and manual measurements.
Auto Intervals: 2.5, 3-10, 15, 20, 30, 45, 60, 90, 120 min.
STAT Mode: Maximum number of measurements in
5 minutes, not to exceed 10.
Displayed Pressures: Systolic, Diastolic, Mean.
Displayed Units: mmHg, kPa.
Systolic Range: 40 to 260 mmHg.
Diastolic Range: 25 to 200 mmHg.
Mean Range: 30 to 220 mmHg.
Pressure Transducer Accuracy: ±3 mmHg.
Redundant Circuit Overpressure Limit: 300 mmHg.
Pulse Rate Range: 40 to 200 bpm.
Typical Measurement Time: 30 seconds.
12-lead ECG and MUSE
Interface (Option)
12 Simultaneously Acquired ECG Leads
12-lead ECG Bandwidth: 0.05 to 150 Hz.
Optional Bandwidth: 0.05 to 40 Hz.
Sampling Rate: 500 sps.
A/D Resolution: 18-bits.
ECG Printing Formats Supported: 4x3 (3 rows, 4 columns,
2.5-10 seconds), 4x3 Cabrera, 4x3 Median Complexes,
2x6 fax only (6 rows, 2 columns, 5 seconds).
Two configurable Custom Lead Groups for 3 Lead strip
chart reports.
GE Medical Systems 12SL Analysis Algorithm:InterpretiveStatements (configurable - ON/OFF),
Global ECG
Measurements, 12-Lead Measurements Matrix
(configurable-ON/OFF).
Fax Transmission: Group 3 Facsimile, 24 Preprogrammed
Phone Numbers (each with 20 digits), Manual Dial
Option, Pulse/Tone Option, Cellular phone-compatible
modem, 11-Digit Alphanumeric Site and Device Identifier.
Patient Demographics: Patient Name, Patient ID
(automati-cally
generated or manually entered), Age, Gender.
IBP (Option)
Number of Channels: 2
Transducer Requirements:
Excitation Voltage: 2.5 V dc.
Transducer Output: 5µV/V/mmHg.
Input Impedance: minimum 250 ohms.
Output Impedance: maximum 3000 ohms.
Pressure Range: -50 to 300 mmHg.
Offset Range: ±200 mmHg.
Accuracy: ±2% measurement or, ±2 mmHg,
whichever is greater, not including transducer.
IBP Safety: per EN60601-2-34.
Temperature (Option)
Number of Channels: 2.
Probe Requirement: YS1 400 compatible.
Temperature Measurement Range: 15 to 45°C.
Resolution: 0.1°C, not including sensor.
General
Size: 10.2 in (25.9 cm) high x 10.3 in (26.2 cm)
wide x 8.7 in (22.1 cm) deep.
Weight: 17.2 lb. (7.82 kg) with Multi-Function
Cable and battery; 19.2 lb. (8.4 kg) with paddles
and battery.
Design Standards: Meets or exceeds UL 2601,
AAMI DF-39, AAMI DF-2, and IEC 601-2-4.
Patient Safety: All patient connections are
electrically isolated.
Environmental: Operating Temperature: 0° to 50°C; Storage
and Shipping Temperature: -20° to 60°C; Humidity: 5 to
95% relative humidity, non-condensing; Vibration: Mil Std
810E, Minimum Integrity Test; Shock: IEC 68-2-27, 50g
6mS half sine; Operating Pressure: 594 to 1060 mBar;
Material Ingress: IEC 529, IP23; Electromagnetic
Compatibility (EMC): CISPR; 11 Class B Radiated and
Conducted Emissions; Electromagnetic
Immunity: AAMI DF-2: IEC 801-3 to 20 V/m;
Electrostatic Discharge: AAMI DF-2: IEC 1000-4-2;
Conducted Susceptibility: IEC 1000-4-4, 1000-4-5,
1000-4-6.
Options: Xtreme Pack™ I Carry Case
Xtreme Pack™II Durable Rubber Case for added protection.
Specifications subject to change without notice.
Rectilinear Biphasic, RescueNet and Xtreme Pack
are trademarks of ZOLL Medical Corporation
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