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The safety of BEMER devices is particularly important to them. Checking the product quality is therefore an indispensable part of their quality assurance measures. Extensive safety tests are carried out at the end of each production process. They also work closely with the responsible authorities beyond the borders of Europe. So they  are e.g. B. with the FDA (one of the most powerful authorities in the USA for the approval and market surveillance of medical devices) and their products are declared as medical devices class II. As a participant in the Medical Device Single Audit program, BEMER Int. AG that it adheres to the currently highest, globally applicable quality standards of the medical technology industry.

Contact :

Phone : +423 399 39 99

Email : [email protected]

Address : Austrasse 15, 9495 Triesen, Liechtenstein