Autobio Labtec Instruments Co.,Ltd.

1.The technical documentation and the EU declaration of conformity are drawn up. 2.In the case of devices for performance studies intended to be used in the context of interventional clinical performance studies or other performance studies involving risks for the subjects, the statement referred to in Section 4.1 of Annex XIV is issued. 3.Other works related with the regulations

1.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 post-market surveillance obligations are complied with in accordance with Article 10(9); 3.The reporting obligations referred to in Articles 82 to 86 are fulfilled,including critical incident and site safety corrective action reporting and analysis, trend reporting and implementation actions.

1.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 post-market surveillance obligations are complied with in accordance with Article 10(9); 3.The reporting obligations referred to in Articles 82 to 86 are fulfilled,including critical incident and site safety corrective action reporting and analysis, trend reporting and implementation actions.