On 8 July 2021 an amendment to the Regulation on Medical Devices MDR (EU) 2017/745 was published in the Official Journal of the European Union (OJ L241/7), highlighting some changes to correct, among other things, misprints, typos and translation errors.

Amendment of MDR (EU) 2017/745|OJ L241/7 08/07/2021
Amendment of MDR (EU) 2017/745|OJ L241/7 08/07/2021

What are the most significant changes?

Among the amendments included in the Amending Document, the most significant are:

  • On page 104, attachment I, Chapter III, point 23.2, letters (c) and (d) General safety and performance requirements, the word “legally” has been added to registered office, as shown in the table below.
instead of should be read as
“ (c) the name, trade name or registered trade mark of the manufacturer and the address of its registered office;” “ (c) the name, trade name or registered trade mark of the manufacturer and the address of its legally registered office;”
“ (d) if the manufacturer has its registered office outside the Union, the name of the authorised representative and the address of their legally registered office;” “ (d) if the manufacturer has its legally registered office outside the Union, the name of the authorised representative and the address of their legally registered office;”
  • At page 143, attachment VIII, Chapter III, point 5.4 (Rule 8), fourth indent Classification Rules the risk class has been changed: Implantable Medical Devices undergoing post-implantation modifications from Class IIb to Class III, as shown in the following table.
instead of should be read as
“– are intended to undergo a chemical modification after introduction into the body, in which case they belong to Class IIb, except when placed in the teeth,” “– are intended to undergo a chemical modification after introduction into the body, in which case they belong to Class III, except when placed in the teeth,”

For more details and to know all the changes made to the MDR (EU) 2017/745 please consult the document published at the following link: https://bit.ly/2UdWKHn

Trust Thema to help you comply with the MDR (EU) 2017/745 Regulation!

There are many tasks to be completed and requirements to be met in order to comply with the Medical Devices Regulation MDR (EU) 2017/745.

Don’t waste any more time!

Contact us to  request valuable strategic regulatory consulting.

Source:

Official Journal of the European Union, OJ L 241/7 08.07.2021