Documenting quality and efficiency

Quality is at the center of everything we do in Medidyne. We aim to distribute medical devices of the highest quality, and it is always with quality in mind that we seek out and evaluate new suppliers and products. In our day-to-day operations, we work in accordance with defined procedures and processes to ensure our customers not only purchase quality products and solutions but receive quality service and support throughout all their interactions with our company.

We continuously adjust the way we work and update our processes and procedures to meet ever-changing market demands and regulatory requirements. In this regard, certificates play a significant role, as they enable us to demonstrate to customers, partners, and other stakeholders that we practice what we preach: We conduct business according to well-defined, effective processes and procedures to maintain a high quality throughout all activities in the company.

ISO 13485 certification

The entire Medidyne organization is ISO 13485 certified. This certification documents that we have an effective system for managing quality in the company.

The ISO 13485 sets requirements for quality management systems in companies working with medical devices in one or more stages of the product life cycle from product design to service and support. The internationally agreed standard helps organizations to consistently meet customer and applicable regulatory requirements for safety and quality in the medical devices industry.

Medidyne A/S, Medidyne AB, Medidyne AS and Medidyne Oy has been certified according to EN ISO 13485:2016 by Bureau Veritas.

ISO 13485 Management System Certification by Bureau Veritas