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HALMED Regulation

Regulation (EU) 2023/607

Transitional provisions for certain medical devices and IVDs, as they apply in Croatia
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Regulation (EU) 2023/607 is the official HALMED identifier for “Transitional provisions for certain medical devices and IVDs, as they apply in Croatia”. Regulation (EU) 2023/607 is the official identifier HALMED 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 Croatia

Union instrument, expressed once in eu.ts as eu-regulation-2023-607. This Croatian row is a metadata view onto that expression. It matters to Croatia 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), decide how long those certificates remain a route into the Croatian market — and because the Croatian act’s own register of devices, its annual maintenance fees and the Agency’s vigilance duties all run on the certificates in circulation rather than on the Regulation’s own conformity assessment. It is not a second corpus copy.

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

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