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General| Category | Medical Equipment |
|---|---|
| Model Series | ProSim 8 Series |
| Manufacturer | Fluke Biomedical |
| Type | Vital Signs Simulator |
| ECG Simulation | Yes |
| Defibrillator Testing | Yes |
| Pacemaker Simulation | Yes |
| Respiration Simulation | Yes |
| Temperature Simulation | Yes |
| Blood Pressure Simulation | Yes |
| Cardiac Output Simulation | Yes |
| Display | Color LCD |
| Connectivity | USB |
| Power Source | Battery |
| Measurement Parameters | ECG, Respiration, Temperature, Cardiac Output |
| ECG Waveforms | Multiple waveforms |
| Respiration Waveforms | Multiple respiration patterns |
| IBP Simulations | Invasive Blood Pressure simulations |
| NIBP Simulations | Non-Invasive Blood Pressure simulations |
| Fetal/Maternal Simulations | Fetal ECG, uterine activity, and maternal ECG |
| Arrhythmia Simulations | Multiple arrhythmia types |
| Performance Waveforms | Square, sine, triangle, pulse, ramp |
Procedures for receiving and inspecting the instrument upon arrival.
Contact information and methods for obtaining application support and technical assistance.
Process for filing claims for physical damage or operational issues.
Guidelines for freight-prepaid shipment, recommended carriers, and insurance for returns.
Information on finding service centers and the calibration recommendation for the product.
Critical warnings regarding unauthorized modifications and their potential hazards.
Specifies the location where the ProSim 8 Vital Signs Simulator is manufactured.
Defines the purpose and target users of the Vital Signs Simulator.
Essential safety guidelines to prevent injury and ensure proper product operation.
Precautions for electrical hazards, usage environments, and connections.
Guidelines for battery handling, replacement, power cord usage, and charging.
Strict prohibition against connecting the product directly to patients or patient-connected equipment.
Precautions for battery disassembly, storage, and handling of hazardous chemicals.
Safety measures for cleaning, using replacement parts, and authorized repairs.
Key operating parameters including temperature, humidity, size, and display type.
Details on USB, wireless, and virtual COM port settings for data communication.
Information on the power source, battery life, and charger specifications.
EMC standards and compliance details for international, Korean, and US regulations.
Specifications for ECG reference, rhythm, output, and amplitude variations.
Detailed parameters for ECG rate, accuracy, waveform selection, and ST-segment elevation.
Specifications for pacer-pulse amplitude, width, arrhythmias, and default settings.
Comprehensive list and descriptions of various cardiac arrhythmias simulated by the device.
Specifications for symptomatic tachycardia types and irregular tachycardia waveforms.
Detailed specifications for R-wave, QRS, and Tall T-Wave detection features.
Information on ECG artifacts, fetal/maternal heart rate, and pressure waveforms.
Specifications for IBP channels, impedance, range, sensitivity, and accuracy.
Parameters for dynamic waveforms, pressure variability, and cardiac catheterization.
Details on respiration artifact, BP output, rate, waves, and impedance variations.
Parameters for temperature measurement, accuracy, compatibility, and output.
Specifications for cardiac output simulation, calibration, injectate, and connector types.
Specifications for NIBP pressure units, manometer, source, and simulation parameters.
Specifications for leak testing, including target pressure, elapsed time, and range.
Parameters for SpO2 % O2 accuracy, saturation, and heart rate measurement.
Specifications for SpO2 transmission ratio, pulse amplitude, and artifacts.
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