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P-9-2019-002465

Zertifizierung durch benannte Stellen gemäß Medizinprodukte-Verordnung (EU 2017/745) und Verordnung für In-Vitro Medizinprodukte (EU 2017/746)

answeredEuropean Union· European Parliament· DE

Introduced

26 July 2019

Last action

13 September 2019 · Answer

Status

answered

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Claudia GAMON

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Discovery layer

Source updated

13 September 2019

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  • English

    Certification by notified bodies under the Medical Devices Regulation (MDR)(EU 2017/745) and the In Vitro Diagnostic Medical Devices Regulation (IVD) (EU 2017/746)

Records

Official record P-9-2019-002465 from European Union at European Parliament. Dated 26 July 2019. Status: answered.

Timeline

  1. 26 July 2019

    Written question

    Zertifizierung durch benannte Stellen gemäß Medizinprodukte-Verordnung (EU 2017/745) und Verordnung für In-Vitro Medizinprodukte (EU 2017/746)

    Source: QUESTION_WRITTEN_PRIORITY

  2. 13 September 2019

    Answer

    Source: QUESTION_WRITTEN_ANSWER

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  • Answer

    QUESTION_WRITTEN_ANSWER · 13 September 2019

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  • Zertifizierung durch benannte Stellen gemäß Medizinprodukte-Verordnung (EU 2017/745) und Verordnung für In-Vitro Medizinprodukte (EU 2017/746)

    QUESTION_WRITTEN_PRIORITY · DE · 5 August 2019

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  • Zertifizierung durch benannte Stellen gemäß Medizinprodukte-Verordnung (EU 2017/745) und Verordnung für In-Vitro Medizinprodukte (EU 2017/746)

    QUESTION_WRITTEN_PRIORITY · DE · 5 August 2019

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  • Certification by notified bodies under the Medical Devices Regulation (MDR)(EU 2017/745) and the In Vitro Diagnostic Medical Devices Regulation (IVD) (EU 2017/746)

    QUESTION_WRITTEN_PRIORITY · EN · 5 August 2019

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  • Certification by notified bodies under the Medical Devices Regulation (MDR)(EU 2017/745) and the In Vitro Diagnostic Medical Devices Regulation (IVD) (EU 2017/746)

    QUESTION_WRITTEN_PRIORITY · EN · 5 August 2019

    DownloadOpen at official source

    Leesvertaling

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  • Certification by notified bodies under the Medical Devices Regulation (MDR)(EU 2017/745) and the In Vitro Diagnostic Medical Devices Regulation (IVD) (EU 2017/746)

    QUESTION_WRITTEN_PRIORITY · EN · 31 July 2019

    ViewDownloadOpen at official source

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  • Certification by notified bodies under the Medical Devices Regulation (MDR)(EU 2017/745) and the In Vitro Diagnostic Medical Devices Regulation (IVD) (EU 2017/746)

    QUESTION_WRITTEN_PRIORITY · EN · 31 July 2019

    ViewDownloadOpen at official source

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  • Certification by notified bodies under the Medical Devices Regulation (MDR)(EU 2017/745) and the In Vitro Diagnostic Medical Devices Regulation (IVD) (EU 2017/746)

    QUESTION_WRITTEN_PRIORITY · EN · 31 July 2019

    DownloadOpen at official source

    Leesvertaling

    Vertaal dit document naar jouw taal. PoliticalRepo bewaart geen aparte kopie per EU-taal.

    Documentvertaling op verzoek met downloadbare PDF (logo + link naar de officiële bron). Het bronbestand blijft leidend.

  • Zertifizierung durch benannte Stellen gemäß Medizinprodukte-Verordnung (EU 2017/745) und Verordnung für In-Vitro Medizinprodukte (EU 2017/746)

    QUESTION_WRITTEN_PRIORITY · DE · 31 July 2019

    ViewDownloadOpen at official source

    Reading translation

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  • Zertifizierung durch benannte Stellen gemäß Medizinprodukte-Verordnung (EU 2017/745) und Verordnung für In-Vitro Medizinprodukte (EU 2017/746)

    QUESTION_WRITTEN_PRIORITY · DE · 31 July 2019

    DownloadOpen at official source

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  • Zertifizierung durch benannte Stellen gemäß Medizinprodukte-Verordnung (EU 2017/745) und Verordnung für In-Vitro Medizinprodukte (EU 2017/746)

    QUESTION_WRITTEN_PRIORITY · DE · 31 July 2019

    ViewDownloadOpen at official source

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