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The Central Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices coordinates the drug surveillance activities of the Federal Länder. It carries out the tasks of the 16 Federal Länder in CE marking for medical devices from higher risk classes with regard to the licensing, designation and monitoring of the independent testing laboratories and certification bodies.*
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via e-mail: email@example.com
or by phone
Monday to Thursday from 9 a.m. to 4 p.m. and
Friday from 9 a.m. to 3 p.m.