Customer information MDR
Dear Sir or Madam,
next year, on 26 May 2021, the new EU Medical Device Regulation (MDR) 2017/745 will come into force and poses a major challenge to companies, manufacturers, dealers, workshops and of course technicians. From this date on, all medical devices that are placed on the market must comply with the new requirements of the MDR.
Streifeneder ortho.production GmbH is currently working with the utmost care on all necessary adaptations and will convert all medical products from the different product ranges in due time. For our customers, therefore, nothing will change - they can continue to rely on the usual performance and quality and do not have to expect any restrictions or bottlenecks.
Part of the new MDR is also the so-called UDI code (Unique Device Identification). This code is only required for medical devices of class I from 26 May 2025 on, but will be implemented on all corresponding products of Streifeneder ortho.production GmbH in the near future. The code provides valuable information and ensures the traceability and transparency of the individual products.
Detailed information on the new MDR can be found on the official website of eurocom e. V..
Please do not hesitate to contact us if you have any questions.
Your Streifeneder ortho.production GmbH