Medical devices directive (93/42/EEC)

DEKRA is Notified Body for the Medical devices directive (93/42/EEC)

No matter how global market conditions change in the future, with DEKRA you’re always a step ahead. As a notified body (ID number 0124), DEKRA has access to experts in all major fields of modern medical technology.

Medical devices directive (93/42/EEC)

Transparency as the new standard

In our complex world, clarity is priceless. Before every project, DEKRA tells you which steps are required for the certification process and estimates the time and costs involved. This lets you know from the very beginning what to expect.

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