Health / Medical Topics |
Device Vibration Problem Evaluation Result
Device problems caused by the constant rhythmic motion of the device, a device's component, or something in the environment to which the device is exposed. (Food and Drug Administration)
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Questioning a pre-defined group of users about their practices.
Any testing performed that simulates real use situations experienced by users.
Terminology used in Individual Case Safety Reports to specify a type of device usage, section H8 of FDA MedWatch Form.
An unused device that has been returned in packaging that remains intact.
The device software contained code that could never be executed under any circumstance.
Testing of individual hardware or software components or groups of related units.