A reliable, easy-to-use, and cost-effective ECG device for almost any office setting.
- A 12-lead resting ECG that provides accurate measurements
- Optional MEANS ECG interpretation software for a second opinion
- High-resolution thermal printer generates full-sized standard and customized reports
- Lead quality graphic saves valuable time by highlighting poor connections
- Full alphanumeric keyboard and LCD screen for easy patient data entry
Dimensions: 15.6 in (39.7 cm) X 6.2 in (15.7 cm) X 16.2 in (41.1 cm)
Weight: 11.6 lb (5.3 kg)
Keyboard type: Elastomer keypad with complete alphanumeric keys
Paper type: 8.25 x 11 inches (21 x 28 cm), Z-fold thermal paper, 200 sheets
Thermal printer (internal): Computer-controlled dot array, 8 dots/mm
Thermal paper speeds 10, 25, 50 mm/s
Gain settings:
- Auto ECGs: 5, 10, 20 mm/mV, AUTO
- Rhythm ECGs: 5, 10, 20 mm/mV
Report print formats:
- Auto ECGs: 3x4, 3x4+ 1R, 3x4 +3R, 6x2, 12x1, 6x2 50 mm/s, 6x2 Ext.
- Rhythm ECGs: 3 leads at a time
- Average cycles: 3x4 50 mm/s + 3R, 6x2 50 mm/s + 6R
Frequency range: 0.3 to 150 Hz
Digital sampling rate: > 1,000 samples/second/channel
Pacemaker detection: ANSI/AAMI EC11
Power requirement: Universal AC power supply 100-240 V ~, 50/60 Hz ~, 2.2 A maximum
Fuses
- AC: Time-delay type, 2 amp 250 V rating, Littlefuse 0215002 or equivalent.
- DC (battery fuse): Fast-acting type, 10 amp 32 V rating, Bussman ATC-10 or equivalent.
Lead configurations: Standard, Cabrera
Rechargeable battery:
- Lead acid gel, 6 volt, 5 AH
- Prints up to 100 continuous ECGs per charge
- 12-hour recharging
Filters:
- 0.5 Hz high-performance baseline filter
- 35 Hz muscle-tremor filter
- AC-interference filter 50 Hz or 60 Hz
Safety, EMC, and regulatory compliance:
- ANSI/AAMI EC11* UL60601-1
- CAN/CSA C22.2 No. 601.1 IEC/EN 60601-1
- CAN/CSA C22.2 No. 601.1.1 IEC/EN 60601-1-1
- CAN/CSA C22.2 No. 601.1.2 IEC/EN 60601-1-2
- CAN/CSA C22.2 No. 601.1.4 IEC/EN 60601-1-4
- CAN/CSA C22.2 No. 601.2.25 IEC/EN 60601-2-25
Standard connectivity: SD memory card slot (for use with cards ? 64 MB)
Connectivity with electronic medical records: Supported through the Welch Allyn CardioPerfect workstation software
Electrodes: Rigorously tested for conductivity, adhesion, and hypoallergenic qualities, and exceed all AAMI standards
Cables and wires: Meet or exceed IEC 60601
Environmental operating conditions:
- Temperature: +10° C to +40° C (+50° F to +104° F)
- Relative humidity: 15 - 95% noncondensing
- Altitude: 700 - 1060 hPa
Environmental storage conditions:
- Temperature: -20° C to +49° C (-4° F to +120° F)
- Relative humidity: 15 - 95% noncondensing (30 - 70% for printing)
- Altitude: 500 - 1060 hPa
Protection against electric shock: Class I, internally powered Type CF
Protection against ingress of water, per IEC 60529: IPX0
Mode of operation: Continuous
*Per AAMI EC11:1991/(R)2001 Diagnostic Electrocardiographic Devices, Section 3.1.2.1 Disclosure of cautionary information/ performance characteristics paragraph c) Accuracy of input signal reproduction, the manufacturer shall disclose the methods used to establish overall system error and frequency response. Welch Allyn has used methods A & D, as prescribed in section 3.2.7.2 and 4.2.7.2 of this same standard, to verify overall system error and frequency response. Because of the sampling characteristics and the asynchronism between sample rate and signal rate, digital ECG systems such as the CP 100 and CP 200 may produce a noticeable modulating effect from one cycle to the next, particularly in pediatric recordings. This phenomenon is not physiologic.
