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UDI and the impact on medical devices (Part 2 – Labeling)

from on 22.04.2015

The Food & Drug Administration (FDA) is currently establishing an unique device identification system. In our first post we explained the fundamentals of the UDI system, its rules and special features. In this part, we will give you label examples, provide information on Direct Permanent Marking DPM and talk about FDA’s final rule – and its five basic requirements. Continue reading