Since April 1, 2021, the AiroDoctor manufacturing facility has been certified according to ISO 13485:2016. The certification is specifically aimed at medical devices and falls within the legally regulated area in Germany to ensure conformity according to the current Directive 93/42/EEC (MDD) as well as the European Medical Device Regulation (MDR). The international certificate represents the requirements for a comprehensive quality management system for the design and manufacture of medical devices and also applies to all future product models based on UV-A photocatalysis.

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