What documentation will I need to provide for a Class I reusable device with regards to cleaning under MDR? 1.57K viewsOctober 10, 2022Medical Device 0 Sam Smith11.38K October 19, 2020 0 Comments Spread the loveSpread the love 1 Answer ActiveVotedNewestOldest 0 Blogolu28.38K Posted October 19, 2020 0 Comments Spread the loveAlong with the cleaning instructions and associated validations, Notified Body assessment will also include other areas such as disinfection, sterilization, maintenance, functional testing. Spread the love You are viewing 1 out of 1 answers, click here to view all answers. Login
