European Union · Record · QUESTION_WRITTEN_PRIORITY
P-9-2019-002465
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)
Introduced
26 July 2019
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answered
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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.
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11 official files
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)
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
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
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
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
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
Answer
QUESTION_WRITTEN_ANSWER · 13 September 2019
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
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
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
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
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
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