Laser marking machines perform UDI-compliant marking of medical devices

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The UDI rule for medical devices is a big topic among manufacturers. The deadline for the third phase of the US Food and Drug Administration (FDA) initiated UDI system ends this year. It affects producers of reusable Class III products such as neurological and cardiovascular catheters and several Class III devices that are single use implants and are sterilized (or cleaned and sterilized) before use.

Read More at Medical Device Network

The Industrial Laser Solutions take on this story:

The deadline for the third phase of the US Food and Drug Administration (FDA)'s unique device identification (UDI) system for medical devices ends in 2016, so medical device makers who produce neurological and cardiovascular catheters, heart valves, pacemakers, and the like must mark their products with a UDI code by September. Recognizing this, FOBA Laser Marking and Engraving will be showcasing its laser marking systems, including a fiber laser solution, at the Medtec show that will take place April 12-14, 2016, in Stuttgart, Germany.

Related: Lasers for medical device marking


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