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Certified according to EN ISO 13485:2016

ISO 13485 contains detailed requirements for the design, manufacturing and placing on the market of medical devices. Its core requirements are product safety and effectiveness. Since 2024, pro aqua meets the high standards for the production of medical devices and can provide official proof of this.

Seit 2024 erfüllt die pro aqua die hohen Standards für die Produktion von Medizinprodukten und kann dies offiziell nachweisen.

Certified according to EN ISO 9001:2015

By fulfilling the requirements of EN ISO 9001, pro aqua demonstrates its highly developed quality management system. Within the company, however, quality is not only fulfilled in the form of requirements, but is actually practiced on a daily basis. We are deeply committed to our culture of continuous improvement.