Until a couple of years ago, the Food and Drug Administration required a unique identifier on each distinct assembly of a medical device in human- and machine-readable forms. That rule has changed. Now, every individual component in an assembly must be marked as well. Traceability is becoming more and more prevalent, not only in the medical device sector but throughout manufacturing.
Source article: https://mfgaxis.com/press-releases/choosing-a-parts-marking-method-depends-on-the-application/
Company: 2L inc.
Press Release: Choosing a parts-marking method depends on the application
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