Dirigeants et représentants réglementaires de Ferrer
SAMPEDRO Cristina
Forward to the manufacturer any request by CA of MS in which the AR has its registered place of business for samples, or access to a device and verify that the competent authority receives the samples or is given access to the device. Immediately inform the manufacturer about complaints and reports about suspected incidents related to a device for which they have been designated. Terminate the mandate if the manufacturer acts contrary to its obligations under MDR
Masqué
GARCIA Laura
Verify the DoC, the TD and the conformity assessment. Keep available a copy of the TD, the DoC and a copy of the relevant certificate. Comply with the registration obligations laid down in Article 31 and verify that the manufacturer has complied with Articles 27 and 29. Provide that CA with all the information necessary to demonstrate the conformity of a device. Terminate the mandate if the manufacturer acts contrary to its obligations under MDR
Masqué
RODELLAS Cristina
Cooperate with the competent authorities on any preventive or corrective action taken to eliminate or, if that is not possible, mitigate the risks posed by devices. Immediately inform the manufacturer about complaints and reports from healthcare professionals, patients and users about suspected incidents related to a device for which they have been designated. Terminate the mandate if the manufacturer acts contrary to its obligations under MDR.