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Biomaterials play an increasingly important role as a replacement of or support for organs that no longer function.
In order to avoid harmful effects that – in the worst case – may lead to the death of a patient, evidence is needed that all relevant medical and safety-related legal requirements have been met. This evidence is warranted by the CE mark.
To evaluate biocompatibility, we offer you certificates, which you can use for CE admission of your devices.
We support you with regard to the following:
– CE marking of medical devices
– official accreditation of medical devices
– international registration of new products
– statements of biological safety evidences |
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