Health / Medical Topics |
Device Light Testing Evaluation Method
Testing the device's characteristics when subjected to variations of ambient light within its surroundings. (Food and Drug Administration)
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Testing the optical properties of a device such as diopter, glare, and irradiance or glistening.
Insufficient, inadequate, or incorrect information provided on a device's label or documentation regarding e.g. as the intended use, directions for use, and…
Reviewing all labeling (including instructions for use, manuals, and packaging) for language related to reported device problems.
Device problems that occur as the result of problems with the labeling (including package inserts, instruction manuals, instructions for use).
Support contact information for a device labeler.
An individual that labels a device.