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All good things come in threes!

QUESTALPHA has performed another crucial step in becoming an independent and certified manufacturer of medical devices.

We are happy to finally being able to present our Certification according to MDSAP and EN ISO 13485, as well as MDR.

The Certification refers to the sales and marketing of Medical Devices of classes I and II and is the result of a successfully completed auditing through our notified body at the beginning of this year.

The entire QUESTALPHA team is proud of having achieved this and is looking forward to advancing even further!