The Medical Device Regulation (MDR) ensures improved safety standards in the manufacture of medical devices. The goal of increasing patient trust in medical technology and ensuring reliable healthcare poses a number of challenges for medical device manufacturers. When implementing the MDR, manufacturers are often dependent on the support of their suppliers along the entire supply chain. ODU deals intensively with the provisions of the MDR and supports its customers in implementing the requirements.
For more than 80 years, ODU's own research and development has been the most important basis in the manufacture of connectors and cable assembly at the highest level. Changing conditions and new requirements are always taken into account. The connector manufacturer has also familiarized itself with the requirements and guidelines on the subject of MDR and keeps up to date with all changes and updates to ensure that the processes in the background are always compliant. This applies both to the standard portfolio and to the tailor-made solutions, in which ODU works closely with its customers – so individual requirements can be taken into account and connectors can be designed that fit perfectly with the desired applications and at the same time comply with the MDR guidelines.
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