FTM AMBALAJ MEDİKAL İTH. İHR. SAN. VE TİC.LTD. ŞTİ

1. appropriate check of the conformity of the aforementioned devices in accordance with the quality management system under which such devices are manufactured and before such device is released. 2.drawing up and keeping up to date of the technical documentation and the EU declaration of conformity of aforementioned devices 3. fulfillment of the post-market surveillance obligations in accordance with Article 10(10) 4.fulfillment of reporting obligations referred to in Articles 87 to 91

1. appropriate check of the conformity of the aforementioned devices in accordance with the quality management system under which such devices are manufactured and before such device is released. 2.drawing up and keeping up to date of the technical documentation and the EU declaration of conformity of aforementioned devices 3. fulfillment of the post-market surveillance obligations in accordance with Article 10(10) 4.fulfillment of reporting obligations referred to in Articles 87 to 91