2020/ÜTSG-3 DATA CHANGE REQUESTS IN IMPORTED PRODUCT RECORDS
Individual follow-up processes have been initiated for optical products as of 11.09.2017, for medical devices within the scope of the Active Implantable Medical Devices Regulation as of 02.07.2018, and for medical devices with class III risk level within the scope of the Medical Device Regulation as of 01.10.2018.
2020/ÜTSG-3 DATA CHANGE REQUESTS IN IMPORTED PRODUCT RECORDS
Individual follow-up processes have been initiated for optical products as of 11.09.2017, for medical devices within the scope of the Active Implantable Medical Devices Regulation as of 02.07.2018, and for medical devices with class III risk level within the scope of the Medical Device Regulation as of 01.10.2018.
2020/ÜTSG-3 DATA CHANGE REQUESTS IN IMPORTED PRODUCT RECORDS
Individual follow-up processes have been initiated for optical products as of 11.09.2017, for medical devices within the scope of the Active Implantable Medical Devices Regulation as of 02.07.2018, and for medical devices with class III risk level within the scope of the Medical Device Regulation as of 01.10.2018.
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Our sales team will contact you as soon as possible.
Please fill out the form below correctly and completely. Our sales team will contact you as soon as possible.
