Immucor GTI Diagnostics, Inc

*Conformity of devices is appropriately checked in accordance with the QMS. *The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. *Post market surveillance obligations are complied with. *The reporting obligations referred to in Regulation (EU) 2017/746 Articles 82 to 86 are fulfilled. *In the case of devices for performance studies, the statement referred to in Regulation (EU) 2017/746 Section 4.1 of Annex XIV is issued

*Conformity of devices is appropriately checked in accordance with the QMS. *Post market surveillance obligations are complied with

*The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date. *The reporting obligations referred to in Regulation (EU) 2017/746 Articles 82 to 86 are fulfilled In the case of devices for performance studies, the statement referred to in Regulation (EU) 2017/746 Section 4.1 of Annex XIV is issued