Sch 5 para 8
In this Schedule— ... “ document ” includes information recorded in any form; “ enforcement order ” means an order under section 156 of the Digital Markets, Competition and Consumers Act 2024 ; “ final enforcement notice ” means a notice under paragraph 16C(2) of this Schedule; “ firm ” means any entity, whether or not a legal person, that is not an individual and includes a body corporate, a corporation sole and a partnership or other unincorporated association; “ interim enforcement order ” means an order under section 159 of that Act; “ interim online interface order ” means an order under section 162 of that Act; “ online interface order ” means an order under section 161 of that Act; “ Regulation (EU) 2017/745 on medical devices ” means Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC , Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC . “ Regulation (EU) 2017/746 on in vitro diagnostic medical devices ” means Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU ; “ the Regulation on Accreditation and Market Surveillance ” means Regulation ( EC ) No 765/2008 of the European Parliament and of the Council of 9 July 2008 setting out the requirements for accreditation and market surveillance relating to the marketing of products and repealing Regulation ( EEC ) No 339/93 . “ the Market Surveillance Regulation ” means Regulation (EU) 2019/1020 of the European Parliament and of the Council of 20 June 2019 on market surveillance and compliance of products and amending Directive 2004/42/EC and Regulations (EC) No 765/2008 and (EU) No 305/2011 ; “ relevant notice ” has the same meaning as in section 202(9) of the Digital Markets, Competition and Consumers Act 2024.