emendrix

Art. 2

Medical Devices Regulation · 32017R0745 · every event for this act · on EUR-Lex

Definitions

1 change recorded across 1 event, newest first.

detected 2026-08-12 MODIFIED+11 −10

no amending act named

applies from: unchanged

In the definition of manufacturer, the phrase describing marketing under the manufacturer's own identifier changes from "trademark" to "trade mark", a purely formal spelling change with no substantive difference in meaning.

Cited: Art. 2, v1 · Art. 2, v2

text before / after

32017R074502017R0745-20170505

Article 2 Definitions For the purposes of this Regulation, the following definitions apply: (1) medical device means any instrument, apparatus, appliance, software, implant, reagent, material or other article intended by the manufacturer to be used, alone or in combination, for human beings for … 1,258 unchanged words … market for the first time for its intended purpose; (30) manufacturer means a natural or legal person who manufactures or fully refurbishes a device or has a device designed, manufactured or fully refurbished, and markets that device under its name or trademark; trade mark; (31) fully refurbishing, for the purposes of the definition of manufacturer, means the complete rebuilding of a device already placed on the market or put into service, or the making of a new device from used devices, to bring it … 1,364 unchanged words … of Article 2 of Regulation (EU) No 1025/2012; (71) common specifications (CS) means a set of technical and/or clinical requirements, other than a standard, that provides a means of complying with the legal obligations applicable to a device, process or system.