ZVA RegulationRegulation (EU) 2017/745
Regulation (EU) 2017/745 is the official ZVA identifier for “Medical Devices Regulation (MDR) as it applies in Latvia”. Regulation (EU) 2017/745 is the official identifier ZVA uses for this instrument.
- Instrument
- Regulation
- Full name
- Regulation (EU) 2017/745
- Category
- Registration
- Authority source
- English
- Readable HTML
- Section view of Regulation (EU) 2017/745
- 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.
Medical Devices Regulation (MDR) as it applies in Latvia
Latvia is an EU member State, so Regulation (EU) 2017/745 applies directly and sits above Cabinet Regulation No. 461, which supplies the national notification, LATMED, authorisation and vigilance machinery the Regulation leaves to member States. The text is expressed once in eu.ts as eu-mdr-2017-745; this row is the Latvian metadata view onto it and opens the articles the national layer hangs off: 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 ZVA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.