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ZVA Regulation

Regulation (EU) 2023/607

Transitional provisions for certain medical devices and IVDs, as they apply in Latvia
LatviaZVARegistration
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Regulation (EU) 2023/607 is the official ZVA identifier for “Transitional provisions for certain medical devices and IVDs, as they apply in Latvia”. Regulation (EU) 2023/607 is the official identifier ZVA uses for this instrument.

Instrument
Regulation
Full name
Regulation (EU) 2023/607
Category
Registration
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This metadata row is a virtual view. The official text is ingested once as Regulation (EU) 2023/607.
Dates
Published
March 20, 2023
Effective
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About this regulation

Transitional provisions for certain medical devices and IVDs, as they apply in Latvia

Union instrument, expressed once in eu.ts as eu-regulation-2023-607. This Latvian row is a metadata view onto that expression. It matters to Latvia because the transitional periods it set for devices covered by a valid Directive 90/385/EEC or 93/42/EEC certificate (Article 120(3a) to (3f) MDR), and the corresponding IVDR period in Article 110(4), determine how long those certificates remain a route into the Latvian market. It is not a second corpus copy.

Regulation (EU) 2023/607 is the official identifier ZVA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.

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