Dirigeants et représentants réglementaires de Sutter Medizintechnik GmbH
SUTTER Bert
Responsibility under article 15 MDR primarily is that: - the conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released and - the technical documentation and the EU declaration of conformity are drawn up and kept up-to-date (Article 15 MDR, 3 (a) and (b)). The responsible person will also act as substitute / deputy for other appointed responsible persons under article 15 MDR.
Masqué
PESCHL Simone
Responsibility under article 15 MDR primarily is that: - the post-market surveillance obligations are complied with in accordance with Article 10(10) and - the reporting obligations referred to in Articles 87 to 91 are fulfilled (Article 15 MDR, 3 (c) and (d)). The responsible person will also act as substitute / deputy for other appointed responsible persons under article 15 MDR.
Masqué
Catalogue des dispositifs de Sutter Medizintechnik GmbH
Aucun dispositif enregistré pour ce fabricant.
Santé des certificats de Sutter Medizintechnik GmbH