The entire Geistlich product portfolio has been successfully certified according to MDR – well before the official transition period. The pioneer in medical regeneration thus confirms its claim to meet the highest quality and safety standards.
As one of the first companies in its field, the regeneration specialist Geistlich has successfully completed the approval process for its entire product portfolio in accordance with the new Medical Device Regulation (MDR) of the European Union (EU) 2017/745. Geistlich thus meets the highest European standards of quality, safety and performance for medical devices—read more.
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