TÜV SÜD Danmark ApS receives designation as Notified Body in accordance with MDR 2017/745
TÜV SÜD Danmark ApS today received its designation as Notified Body 2443 under Medical Device Regulation 2017/745 by the…
TÜV SÜD Danmark ApS today received its designation as Notified Body 2443 under Medical Device Regulation 2017/745 by the…
TÜV SÜD is one of the few notified bodies that still has capacities for conformity assessment procedures for medical dev…
It’s done! Hemovent successfully completed the Medical Device Regulation (MDR 2017/745) certification process for its MO…
On 6 January 2023, the European Commission published a proposal to amend the Medical Device Regulation (MDR) and the In…
The presentation of the processes around the Medical Device Regulation (MDR), which will now become valid on 26 May 2021…
On 26 May, 2020, the Medical Device Directive (MDD) will be replaced by the new Medical Device Regulation (MDR). MDR is…
The audit, which took place from January 27 to 29, confirmed that Richard Wolf GmbH is compliant with the MDR. This mean…
TÜV Rheinland LGA Products GmbH is now a notified body for the EU Medical Device Regulation (MDR) 2017/745. The European…
. Introduction The MDR (Medical Device Regulation) is currently a hot topic and is keeping manufacturers of medical pr…
Trevira GmbH, the specialist for functional fibres and yarns, will be exhibiting at the Techtextil in Frankfurt in May t…