Malsfeld – Dr. Schumacher GmbH has successfully received certification for a selected product range under the European Medical Device Regulation (MDR). As one of the first manufacturers of disinfection and hygiene solutions, Dr. Schumacher is now officially confirmed as MDR-compliant for a selected range of products. With the final certification now granted by the notified body, Dr. Schumacher offers its customers several MDR-compliant medical devices and ranks among the MDR pioneers in the disinfection, hygiene, and wipe segments.
The MDR certificate applies to medical devices in product classes IIa and IIb. With this certificate, Dr. Schumacher assures its customers and business partners access to MDR-compliant medical products for both drugstores and retail sectors.
Dr. Schumacher has worked for several years with the notified body to implement the stringent requirements of the EU regulation as quickly as possible. Following a successful audit in 2022 and a re-certification the following year, Dr. Schumacher has now received its MDR certificate for a selected product range.
With this MDR certificate, the family-owned company is authorized to bring innovations to market (depending on classification, in collaboration with the notified body) and to further develop existing products for sale. With the confirmation of MDR compliance for the selected range, Dr. Schumacher is now returning its focus to its highest priority: developing safe products that are simple and convenient to use everywhere.
The Medical Device Regulation (MDR) harmonizes existing regulations and requirements for medical device manufacturers across the European Union. It protects patient health and improves the safety of healthcare providers. In addition, the MDR establishes clear guidelines on the efficacy and application areas of various medical devices, ensuring greater transparency.
Contact:
Jens Thumser
Company Spokesperson and Head of Corporate Communications
T +49 5664 9496-2030
presse@schumacher-online.com
