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General| Category | Medical Equipment |
|---|---|
| Technology | Capacitive |
| Interface | USB |
| Measurement Principle | Capacitive pressure measurement |
| Sensor Type | Pressure Sensor |
| Applications | Rehabilitation |
| Measurement Range | Up to 120 N/cm² |
| Sensor Area | Various sizes available (depending on the model) |
Contact details and address of zebris Medical GmbH.
Explains warning, note symbols, and general conventions used in the manual.
Details the system's application, classification, and operational guidelines.
Covers essential safety instructions, warnings, and prohibited uses of the device.
Lists the basic components included in the FDM measuring system.
Specifies the minimum hardware and software requirements for the PC.
Explains how the FDM system measures pressure distribution using capacitive sensors.
Details interfaces, operating voltage, power, temperature, and measuring range of the sensor.
Provides technical specifications for FDM-SX and FDM-S force plate models.
Details technical data for FDM 1.5, FDM 2, and FDM 3 systems.
Provides input, output, cable length, and pin arrangement for the power supply.
Ensures the platform is set up on an even, horizontal surface.
Explains the meaning of different LED states (green/orange flashing/permanent).
Describes how the platform is controlled via software and the operating indicator.
Details required components, connections, and software installation for setup.
Steps to safely shut down and disconnect the FDM system.
Explains synchronization with video cameras via the Sync-Audio socket.
Describes infrared synchronization with zebris DAB-Bluetooth for EMG data.
Instructions for linking two platforms (Master-Slave) to expand the walking range.
Details synchronizing the FDM system with external devices via sync ports.
Guidance on setting up an optimal walking range for accurate measurements.
Instructions for proper data recording, focusing on foot contact on the sensor area.
Recommendations for maintaining consistent gait velocity during measurements.
Covers pre-operation checks, immediate maintenance measures, and authorized servicing.
Describes control measures and calibration checks for sensor accuracy.
Provides instructions for cleaning and disinfecting the platform and accessories.
Specifies that storage and transport should be in original packaging.
Details proper disposal procedures for electronic waste according to directives.
Classifies the FDM system as Class I with measurement function.
Confirms compliance with DIN EN 60601-1 standards, including BF classification.
Notes on combining the system with compliant tools and keeping computers away from patients.
Details EMC compliance, warnings about RF equipment, and accessory cable effects.
EC Declaration of Conformity for medical FDM platforms, listing standards and validity.
EC Declaration of Conformity for non-medical FDM platforms, listing standards and validity.
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