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We act in accordance with Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 (Medical Device Regulation). Pursuant to Section 3 of Medizinprodukte-Abgabeverordnung in conjunction with Section 3 No. 2 of the Medizinprodukte-Durchführungsgesetzes, medical devices that are not intended for use by laypersons may only be supplied to healthcare professionals. We kindly ask you to inform yourself about the latest information on our products and services.