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Ministry of Health Regulation

Regulation (EU) 2017/746

In Vitro Diagnostic Medical Devices Regulation (IVDR) as it applies in Cyprus
CyprusMinistry of HealthRegistrationEffective May 26, 2022
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What this code is

Regulation (EU) 2017/746 is the official CYMDA identifier for “In Vitro Diagnostic Medical Devices Regulation (IVDR) as it applies in Cyprus”. Regulation (EU) 2017/746 is the official identifier CYMDA uses for this instrument.

Instrument
Regulation
Full name
Regulation (EU) 2017/746
Category
Registration
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Authority source
English
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Issuing-authority publication; confirm whether a later amendment or consolidated version applies.
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This metadata row is a virtual view. The official text is ingested once as Regulation (EU) 2017/746.
Dates
Published
May 5, 2017
Effective
May 26, 2022
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About this regulation

In Vitro Diagnostic Medical Devices Regulation (IVDR) as it applies in Cyprus

Cyprus is an EU member State, so Regulation (EU) 2017/746 applies directly; as with the MDR there is no Cypriot instrument restating it. The text is expressed once in eu.ts as eu-ivdr-2017-746; 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) and EUDAMED registration (Arts. 27 to 29). It is not a second corpus copy.

Regulation (EU) 2017/746 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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