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National Organization for Medicines (EOF) 🇬🇷

Description

The National Organization for Medicines, known in Greek as Εθνικός Οργανισμός Φαρμάκων (EOF), serves as Greece's regulatory authority for pharmaceuticals and healthcare products.

Official website

http://www.eof.gr/

Recalls of medical devices

From National Organization for Medicines (EOF) 🇬🇷

Number of entries: 714

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Updated 1 day ago

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Announcement on the European Commission's investigation into the electronic instructions for use of Medical Devices

From National Organization for Medicines (EOF) 🇬🇷

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Updated 2 weeks ago

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Announcement on Medical Devices

From National Organization for Medicines (EOF) 🇬🇷

Announcement on new transitional provisions of Reg. (EU) 2017/746 on In Vitro Diagnostic Medical Devices (IMDs) and on the ...

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Updated on July 29, 2024

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Notice on Medical Devices

From National Organization for Medicines (EOF) 🇬🇷

Notice concerning products applied to the skin with health claims (muscle pain, joint pain, etc.), containing camphor and/or ...

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Updated on July 1, 2024

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Notice on Custom-made technology products

From National Organization for Medicines (EOF) 🇬🇷

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Updated on April 23, 2024

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Participation in training on Medical Devices, NoBoCap, EU4Health (EU4H)

From National Organization for Medicines (EOF) 🇬🇷

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Updated on February 16, 2024

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Communication on the European Medical Device Nomenclature (EMDN)

From National Organization for Medicines (EOF) 🇬🇷

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Updated on February 15, 2024

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NON-INHABITATIVE BLOOD GLUCOSE METER WITH FALSE PRESENTATION AS ACCU-CHEK via www.kioltech.shop/bg and www.fnastypl.monster

From National Organization for Medicines (EOF) 🇬🇷

The EOF draws the attention of consumers to the presentation of the product 'ACCU-CHEK non-invasive glucose glucose meter' with false ...

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Updated on February 9, 2024

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NON-INVASIVE BLOOD GLUCOSE METER FALSELY REPRESENTED AS MEDTRONIC

From National Organization for Medicines (EOF) 🇬🇷

The EOF draws the attention of consumers to the presentation of the product 'non-invasive glucose glucose meter' with the false ...

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Updated on December 22, 2023

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Communication on the European Commission's survey on monitoring the availability of Medical Devices (MD) on the European Union market

From National Organization for Medicines (EOF) 🇬🇷

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Updated on December 6, 2023

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Notice concerning the transitional provisions of Reg. (EU) 2017/745 on Medical Devices (MD)

From National Organization for Medicines (EOF) 🇬🇷

Following the 28-03-2023 Announcement (link) regarding the publication of the ...

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Updated on July 25, 2023

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Announcement on the Unique Designation Identification (UDI) system

From National Organization for Medicines (EOF) 🇬🇷

Following our announcement dated 27-05-2021, we inform you of the current information and detailed instructions that have been ...

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Updated on April 7, 2023

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Notice concerning the publication of Regulation (EU) 2023/607 amending Regulations (EU) 2017/745 and (EU) 2017/746.

From National Organization for Medicines (EOF) 🇬🇷

Please be informed that Regulation (EU) 2023/607 of the European Parliament and of the Council of 15 March 2023 on ...

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Updated on March 28, 2023

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Updated list of self-diagnostic tests (self-tests) for the detection of coronavirus

From National Organization for Medicines (EOF) 🇬🇷

The EOF, for the information of the public, publishes the updated list of self-diagnostic tests (self-tests) that have received ...

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Updated on September 1, 2022

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Information for MD Manufacturers on the requirements of Regulation (EU) 2017/745

From National Organization for Medicines (EOF) 🇬🇷

The EOF informs you about the "MDCG Position Paper_Notice to manufacturers to ensure timely compliance with MDR requirements", which was published on the European Commission's website, ...

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Updated on June 22, 2022

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Updated List of Self Diagnostic Tests for Coronavirus Detection

From National Organization for Medicines (EOF) 🇬🇷

Following the 31/5/2021 Announcement regarding the Coronavirus Detection Tests, the EOF publishes for public information the ...

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Updated on January 5, 2022

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Guidance document with information on the obligations of Importers and Distributors under the Medical Device Regulations (EU) 2017/745 & 746.

From National Organization for Medicines (EOF) 🇬🇷

Please be informed that the document "MDCG 2021-27 - Questions and Answers on Articles 13 & 14 of Regulation (EU) 2017/745 and Regulation (EU) 2017/746" has been published on the European Commission's website, providing ...