Officers and regulatory representatives of Atlas Medical GmbH
BRAISH Noura
1. 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.
2.The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date.
3.the post-market surveillance obligations are complied with in IVDR requirements.
4.Vigilance Reporting to Competent authority.
Hidden
SHTAIWI Saba’a
1. 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.
2.The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date.
3.the post-market surveillance obligations are complied with in IVDR requirements.
4.Vigilance Reporting to Competent authority.