Anwendungsbereich des Regulatory Essentials
This ESSENTIAL focuses on cybersecurity for medical devices.
This ESSENTIAL describes the legal obligations for manufacturers of medical devices in the European Union, based on the
- Regulation (EU) 2017/745 and its amendments
- MDCG (EU Medical Device Coordination Group) documents
Manufacturer, B2C products, B2B products
Geltende Rechtsvorschriften:
Medical Device Regulation (MDR)
NIS-2-Directive (EU) 2022/2555
Publication in Official Journal of the European Union on 27. December 2022.
Transposition by member states by 17 October 2024.
Application of measures by 18 October 2024.
For further information see:
ESS EEA Cybersecurity - Essential and important entities
Nationale Anwendungsebene:
European Economic Area (EU + Iceland, Lichtenstein, Norway)
Published 2024-07-11 by Benjamin Kerger and Anne Barsuhn
Last change 2024-12-16 by Anette Dunkel-Reinboth: User instructions language(s) , Cybersecurity
Inhalt des Regulatory Essentials
| Scope of legislation |
Cybersecurity requirements contained in MDR Annex I (MDCG 2019-16 rev. 1)'
|
| Link/Reference to other reference document(s) |
Hier erhalten Sie textbasierte Informationen
|
| Link/Reference to other reference document(s) |
Hier finden Sie ein thematisch passendes Dokument in ATERIOS
(Zugang nur mit erweiterter ATERIOS Lizenz)
|
| Scope of legislation |
Hier erhalten Sie ein Foto oder Diagram
|
| Responsible actors |
Hier erhalten Sie textbasierte Informationen
Which actor(s) are responsible for compliance with the legal provisions: e. g.
- economic operators (manufacturer, importer, distributor, fulfilment service provider),
- user (commercial/industrial/professional),
- user (private, consumer)?
|
| Process-related requirements? |
Hier erhalten Sie textbasierte Informationen
|
| Product-related requirements? |
Hier erhalten Sie textbasierte Informationen
|
| Regulatory market access conditions for the actor(s) |
Hier erhalten Sie textbasierte Informationen
What are the main regulatory requirements (e. g. conformity assessment fulfilment of essential requirements of Annex I 2006/42/EC) prior placing on the market, importation and putting into service (brief description)
|
| Penalty by this legislation |
Hier erhalten Sie textbasierte Informationen
What are the possible penalties (e. g. sales ban, fines) in the case of non-compliance?
|
| Exemption clauses |
Hier erhalten Sie zugehörige weiterführende Links
Exempted devices/products or industry sectors.
|
| Sub-federal legislation of states/counties |
Hier erhalten Sie textbasierte Informationen
E. g. by 2019 an Inter-Governmental Agreement (IGA) on governance of the Electrical Equipment Safety System (EESS) has been signed by Queensland, Victoria, Western Australia and Tasmania.
|
| FTA/MRA status with EU |
Hier erhalten Sie textbasierte Informationen
Has the country signed a Free Trade Agreement (FTA) or a Mutual recognition agreement (MRA) with EU?
|
| Adequate third countries to transfer data |
Hier finden Sie ein thematisch passendes Dokument in ATERIOS
(Zugang nur mit erweiterter ATERIOS Lizenz)
|
| Adequate third countries to transfer data |
Hier erhalten Sie zugehörige weiterführende Links
|
| Authority |
Hier erhalten Sie textbasierte Informationen
Name of the authority for approval, registration, market surveillance and/or enforcement
|
| Market surveillance authority |
Hier erhalten Sie textbasierte Informationen
Name of the authority for market surveillance and/or enforcement
|
| User instructions language(s) |
Hier erhalten sie eine Tabelle
Regulated by the legal provisions
|
Formal and administrative requirements
|
| Registration at related authority required? |
Hier erhalten Sie textbasierte Informationen
Product registration?
Manufacturer registration?
Importer / Representative registration?
if required.
|
| Local representative legally required? |
Hier erhalten Sie textbasierte Informationen
[Yes/No]
|
Equipment authorization (approval process)
|
| Approval process (conformity assessment procedure) |
Hier erhalten Sie textbasierte Informationen
Means each legally required approval process prior placing on the market, importation or putting into service
|
| Is the IECEE CB Scheme accepted by the authority/approval body? |
Hier erhalten Sie zugehörige weiterführende Links
"[Yes/ No / no information available]
[Text] Information (website)"
|
| Conformance document(s) to show compliance to the authority |
Hier erhalten Sie textbasierte Informationen
e. g. SDoC, technical documentation (for 10 years), filled-in approval forms (e. g. ACMA in AUT)
|
| Conformance document validity and renewal |
Hier erhalten Sie textbasierte Informationen
Validity for Conformance document name mentioned. For mandatory certification validity is important.
|
| Which documents are required by an approval body? |
Hier erhalten Sie textbasierte Informationen
e .g. formal application
|
| Is a factory inspection legally required |
Hier erhalten Sie textbasierte Informationen
|
| Hint to voluntary certification scheme |
Hier erhalten Sie textbasierte Informationen
If a important voluntary certification schemes exists, one link will be given.
Important voluntary schemes are for example: UL, CSA, VCCI (Japan)
|
| Specific requirements for testing |
Hier erhalten Sie textbasierte Informationen
e. g. is an accredited test lab. mandatory, limits, test samples, product description
|
| General information to the application of standards |
Hier erhalten Sie textbasierte Informationen
e. g. China: GB standards are mandatory, EU: harmonized standards shall be published in the OJEU with respect to "presumption of conformity"
|
| Source for standards for conformity assessment |
Hier erhalten Sie zugehörige weiterführende Links
|
| National Standardisation Organisation |
Hier erhalten Sie textbasierte Informationen
Link to organisation
|
| Are national standards based on IEC/ISO standards? |
Hier erhalten Sie textbasierte Informationen
Undetailed information
|
| Is in-country testing legally required? |
Hier erhalten Sie textbasierte Informationen
|
| Acceptance of foreign test reports |
Hier erhalten Sie textbasierte Informationen
|
| Hints |
Hier erhalten Sie textbasierte Informationen
Specific recommendations, information or most common mistakes
|
Regulatory labelling, markings and user information
|
| Regulatory label (mandatory) |
Hier erhalten Sie textbasierte Informationen
e. g. product label
|
| Regulatory e-labelling allowed? |
Hier erhalten Sie textbasierte Informationen
e. g. put the regulatory information and labels in a software menu
|
| Required information on the product and/or packaging |
Hier erhalten Sie textbasierte Informationen
e. g. address of the manufacturer/importer, serial number
|
| User instruction requirements and specific compliance notes |
Hier erhalten Sie textbasierte Informationen
Form, sentence inside, simple text.
E. g. FCC/ISED compliance information, SAR information, battery, environmental information like waste
|
| Digital user documentation allowed? |
Hier erhalten Sie textbasierte Informationen
User instructions allowed by QR-Code/internet or digital medium or integrated in device with display?
Safety instruction allowed by QR-Code or digital medium?
|
| Warnings, symbols |
Hier erhalten Sie textbasierte Informationen
e. g. ANSI Z 535.4
|
Allgemeine Informationen
European Economic Area (EU + Iceland, Lichtenstein, Norway)
Code, Kontinent, Wirtschaftsraum
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