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One year ago, the EU Commission suspended the end of the transition period for the EU Medical Device Regulation (MDR) for one year due to the COVID-19 pandemic. The transition period expired though on 26 May 2021, and thus the MDR applies throughout Europe. The comprehensive reform of the entire European medical device law obviously affects also dental practices and dental laboratories. As a regulation of European law, it is directly applicable and thus replaces the Medical Device Directive MDD. In the summer issue of EDI Journal we provide you with an overview of what is necessary to meet the requirements. We also provide you with with the conformity declaration for download.

Besides we give you an update on one-piece ceramic implants to optimize hard and soft tissue management and give you some instructions to implement ridge preservation into everyday use.

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EDI Journal 4/2022

The path of the BDIZ EDI 2023

EDI-Journal 3/2022

Digitisation in implant dentistry

EDI Journal 2/2022

Guideline 2022: Cologne ABC Risk Score for implant treatment

EDI Journal 1/2022

Perspective: dentistry – Implantology - Europe

EDI Journal 4/2021

How much medicine does dentistry need?

EDI Journal 3/2021

Update ceramics in implantology

EDI Journal 1/2021

Discussion on vitamin D

EDI Journal 4/2020

Quo vadis, implantology?

EDI Journal 3/2020

Bone and soft tissue management

EDI Journal 2/2020

BDIZ EDI support beyond the crisis