TÜV Rheinland, a global provider of testing and certification services, has granted Taiwanese medical device manufacturer GaleMed certification in accordance with the new EU Medical Devices Regulation (MDR).
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As part of EU reforms in recent years, the Medical Device Directive (MDD) has been upgraded to the Medical Device Regulation (MDR), which significantly increases the requirements for safety, performance, clinical evaluation and life cycle of medical devices. TÜV Rheinland, one of the world's leading providers of testing and certification services, offers manufacturers and distributors of medical devices to check their products for MDR conformity.
GaleMed produces respiratory care interface technology such as neonatal and prenatal ventilation. With the current certification, GaleMed and TÜV Rheinland are making an important contribution to the operational implementation of the MDR.
As part of EU reforms in recent years, the Medical Device Directive (MDD) has been upgraded to the Medical Device Regulation (MDR), which significantly increases the requirements for safety, performance, clinical evaluation and life cycle of medical devices. As a result, manufacturers and distributors must comply with stricter requirements in terms of standards, quality and market surveillance.
Recently, manufacturers and importers, as well as physicians, have increasingly pointed out the difficulties in implementing the new requirements and warned of possible shortages of medical devices, especially in the field of paediatrics. Earlier this year, the European Commission held out the prospect of extending the transition periods.
The European Union (EU) is the second largest medical market in the world and imports a large proportion of its medical products from China and Taiwan. In Germany, for example, the share for certain products such as respiratory masks is up to 90%, according to the Kiel Institute for the World Economy (IfW).