Commitment to Quality and Compliance with Regulations RAUMEDIC Offers You Qualified Support

Certified Quality Management

Customer satisfaction and compliance with all relevant legal, normative and regulatory requirements are the focus of our concept of quality. In order to meet these requirements, RAUMEDIC has established a comprehensive certified quality management system:

  • QM system according to ISO 13485
  • Complete quality assurance system according to EC Directive 93/42/EEC 
  • Complete quality assurance system according to EC Directive 90/385/EEC
  • Quality assurance system according to Regulation (EU) 2017/745 on medical devices, Appendix IX Chapters I and III

RAUMEDIC is Manufacturing in a Controlled Environment

Manufacturing processes such as the production of medical products or semi-finished medical products and of pharmaceutical products as well place high demands on the environmental conditions. This is why RAUMEDIC manufactures in a controlled environment:

  • Clean room manufacturing according to ISO 14644, ISO Class 7 (=10,000)
  • GMP orientated manufacturing

CE-Marking for the European Economic Area

The CE declaration of conformity and CE-marking are necessary for placing products in the market within the European economic area. CE conformity assessment procedures for RAUMEDIC medical devices in line with:

  • Appendix II of EU Directive 93/42/EEC
  • Appendix 2 of EU Directive 90/385/EEC
  • Appendix IX of Regulation (EU) 2017/745

Our services for customized developments includes professional support with CE certification processes.

MDR ready… set, go!

Are you ready for the Medical Device Regulation? Get optimal help from our experts and learn how RAUMEDIC can support you during the approval process.