(EU) 2017/745 Medical Device Regulation Certification
(EU) 2017/745 Medical Device Regulation Certification
Category:
Ventilators, nebulizers and respiratory devices
This product is provided by the company SZUTEST UYGUNLUK DEĞERLENDİRME A.Ş. . Please contact for more information.
Product Description
The CE marking indicates that the products comply with the provisions set out in the technical regulations of the EU and can be released into free circulation within the EU without.
SZUTEST Konformitätsbewertungsstelle GmbH is recognized by the Central Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices (ZLG) and EU Commission, as a Notified Body with the identification number 2975 under the Medical Device Regulation (EU) 2017/745.
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