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Ministry of Health Regulation

Regulation (EU) 2017/745

Medical Devices Regulation (MDR) as it applies in Cyprus
CyprusMinistry of HealthRegistrationEffective May 26, 2021
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What this code is

Regulation (EU) 2017/745 is the official CYMDA identifier for “Medical Devices Regulation (MDR) as it applies in Cyprus”. Regulation (EU) 2017/745 is the official identifier CYMDA uses for this instrument.

Instrument
Regulation
Full name
Regulation (EU) 2017/745
Category
Registration
Source links
Authority source
English
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This metadata row is a virtual view. The official text is ingested once as Regulation (EU) 2017/745.
Dates
Published
May 5, 2017
Effective
May 26, 2021
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Each version has stable article anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.

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About this regulation

Medical Devices Regulation (MDR) as it applies in Cyprus

Cyprus is an EU member State, so Regulation (EU) 2017/745 applies directly and is the only retrievable official expression that carries the device obligations a customer asks about — there is no Cypriot instrument that restates them. The text is expressed once in eu.ts as eu-mdr-2017-745; this row is the Cypriot metadata view onto it and opens the articles CYMDA’s notices apply: manufacturer obligations (Art. 10), importer and distributor obligations (Arts. 13 and 14), EUDAMED registration (Arts. 30 and 31) and vigilance (Art. 87). It is not a second corpus copy.

Regulation (EU) 2017/745 is the official identifier CYMDA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.

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