Sahajanand Medical Technologies Limited

To check conformity of devices before their release. To ensure that technical documentation and the EU DOC are drawn up and kept up to date. To ensure compliance of PMS obligation per Article 10 (10). To ensure implementation and keep up to date of PMS system in accordance with Article 83. To Report competent authority/notified body about reportable incidences, FSCA, trend reporting, and other obligations. To ensure precautions during clinical investigation of Investigational Device.