Medical technology:
We put them through their paces.

A lot depends on active medical devices: especially human health. It is no coincidence that the Medical Device Directive (MDR) distinguishes between non-active medical devices and active ones, i.e. those that require an external energy source. However, this is just one of many facts that need to be known in the extensive standards landscape of medical technology and in-vitro diagnostics.

We at SGS-TÜV Saar think ahead: whether electromagnetic compatibility or functional safety; whether biocompatibility or environmental simulation and much more - we advise, test, examine, assess and certify active medical devices. And we are aware of the complexity of the standards landscape and all the innovations that digitality brings with it.