# The Market Surveillance (Northern Ireland) Regulations 2021, Paragraph 1: Interpretation of terms used in this Schedule

Extent: N.I.

In this Schedule—
“premises” includes any trading stall, vehicle, vessel or aircraft;
“proceedings” may include an application for forfeiture.
“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.

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Source: https://www.legislation.gov.uk/uksi/2021/858/schedule/1/paragraph/1 (the official version)
Page: https://openlegislation.uk/market-surveillance-northern-ireland-regulations-2021/schedule-1/paragraph-1
Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives.