| 类型 | 编号 | 名称 | 状态 |
|---|
| 指南 | | MDCG 2020-10/2 rev.1 | in_force |
| 指南 | | Conformity assessment procedures for protective equipment | in_force |
| 指南 | | How to verify that medical devices and personal protective equipment can be lawfully placed on the EU market and thus purchased and used – also in the COVID-19 context | in_force |
| 指南 | | Guidance on regulatory requirements for medical face masks | in_force |
| 指南 | | Guidance on medical devices, active implantable medical devices and in vitro diagnostic medical devices in the COVID-19 context | in_force |
| 指南 | | Conformity assessment procedures for 3D printing and 3D printed products to be used in a medical context for COVID-19 | in_force |
| 指南 | | The EMDN – The nomenclature of use in EUDAMED | in_force |
| 指南 | | The CND nomenclature – Background and general principles | in_force |
| 指南 | | Guidance on the Version History | in_force |
| 指南 | | Article 10a Decision tree | in_force |
| 指南 | | MDCG 2023-2 MDR form | in_force |
| 指南 | | MDCG 2023-2 IVDR form | in_force |
| 指南 | | Manual on borderline and classification under Regulations (EU) 2017/745 and 2017/746 v5 Background note on the use of the Manual on borderline and classification for medical devices under the Directives. | in_force |
| 指南 | | Guidance on sufficient clinical evidence for legacy devices Background note on the relationship between MDCG 2020-6 and MEDDEV 2.7/1 rev.4 on clinical evaluation | in_force |
| 指南 | | COVID-19 TESTS: Q&A on in vitro diagnostic medical device conformity assessment and performance in the context of COVID-19 (available in all EU languages and Arabic , Chinese , Japanese , Russian ) | in_force |
| 指南 | | Background note | in_force |
| 指南 | | Word version | in_force |
| 指南 | CAMD FAQ | CAMD MDR/IVDR Transition Subgroup: FAQ – MDR Transitional provisions | in_force |
| 指南 | Gradual roll out of EUDAMED | Q&A on practical aspects related to the implementation of the gradual roll-out of Eudamed pursuant to the MDR and IVDR, as amended by Regulation (EU) 2024/1860 amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards a gradual roll-out of Eudamed, the obligation to inform in case of interruption or discontinuation of supply, and transitional provisions for certain in vitro diagnostic medical devices1 | in_force |
| 指南 | Helsinki Procedure | Helsinki Procedure for borderline and classification under MDR & IVDR | in_force |
| 指南 | Infographic | Is your software a Medical Device? | in_force |
| 指南 | MDCG 2018-1 rev.4 | Guidance on basic UDI-DI and changes to UDI-DI | in_force |
| 指南 | MDCG 2018-2 | Future EU medical device nomenclature - Description of requirements | in_force |
| 指南 | MDCG 2018-3 rev.1 | Guidance on UDI for systems and procedure packs | in_force |
| 指南 | MDCG 2018-4 | Definitions/descriptions and formats of the UDI core elements for systems or procedure packs | in_force |
| 指南 | MDCG 2018-5 | UDI assignment to medical device software | in_force |
| 指南 | MDCG 2018-6 | Clarifications of UDI related responsibilities in relation to article 16 | in_force |
| 指南 | MDCG 2018-7 | Provisional considerations regarding language issues associated with the UDI database | in_force |
| 指南 | MDCG 2018-8 | Guidance on content of the certificates, voluntary certificate transfers | in_force |
| 指南 | MDCG 2019-1 | MDCG guiding principles for issuing entities rules on basic UDI-DI | in_force |
| 指南 | MDCG 2019-11 rev.1 | Qualification and classification of software - Regulation (EU) 2017/745 and Regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2019-12 | Designating authority's final assessment form: Key information (EN) | in_force |
| 指南 | MDCG 2019-13 rev.1 | Guidance on sampling of devices for the assessment of the technical documentation | in_force |
| 指南 | MDCG 2019-14 | Explanatory note on MDR codes | in_force |
| 指南 | MDCG 2019-15 rev.1 | Guidance notes for manufacturers of class I medical devices | in_force |
| 指南 | MDCG 2019-16 rev.1 | Guidance on cybersecurity for medical devices | in_force |
| 指南 | MDCG 2019-2 | Guidance on application of UDI rules to device-part of products referred to in article 1(8), 1(9) and 1(10) of Regulation 745/2017 | in_force |
| 指南 | MDCG 2019-3 rev.1 | Clinical evaluation consultation procedure exemptions Interpretation of article 54(2)b | in_force |
| 指南 | MDCG 2019-6 rev.5 | Questions and answers: Requirements relating to notified bodies | in_force |
| 指南 | MDCG 2019-7 - rev.1 | Guidance on article 15 of the medical device regulation (MDR) and in vitro diagnostic device regulation (IVDR) on a ‘ person responsible for regulatory compliance ’ (PRRC) | in_force |
| 指南 | MDCG 2019-8 v2 | Guidance document implant card on the application of Article 18 Regulation (EU) 2017/745 on medical devices | in_force |
| 指南 | MDCG 2019-9 - rev.1 | Summary of safety and clinical performance | in_force |
| 指南 | MDCG 2020-1 | Guidance on clinical evaluation (MDR) / Performance evaluation (IVDR) of medical device software | in_force |
| 指南 | MDCG 2020-10/1 rev.1 | Guidance on safety reporting in clinical investigations Appendix: Clinical investigation summary safety report form | in_force |
| 指南 | MDCG 2020-11 | Guidance on the renewal of designation and monitoring of notified bodies under Directives 90/385/EEC and 93/42/EEC to be performed in accordance with Commission Implementing Regulation (EU) 2020/666 amending Commission Implementing Regulation (EU) 920/2013 | in_force |
| 指南 | MDCG 2020-12 | Guidance on transitional provisions for consultations of authorities on devices incorporating a substance which may be considered a medicinal product and which has action ancillary to that of the device, as well as on devices manufactured using TSE susceptible animal tissues | in_force |
| 指南 | MDCG 2020-13 | Clinical evaluation assessment report template | in_force |
| 指南 | MDCG 2020-14 | Guidance for notified bodies on the use of MDSAP audit reports in the context of surveillance audits carried out under the Medical Devices Regulation (MDR)/In Vitro Diagnostic medical devices Regulation (IVDR) | in_force |
| 指南 | MDCG 2020-16 rev.4 | Guidance on Classification Rules for in vitro Diagnostic Medical Devices under Regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2020-17 | Questions and Answers related to MDCG 2020-4: “Guidance on temporary extraordinary measures related to medical device notified body audits during COVID-19 quarantine orders and travel restrictions” | in_force |
| 指南 | MDCG 2020-3 rev.1 | Guidance on significant changes regarding the transitional provision under Article 120 of the MDR with regard to devices covered by certificates according to MDD or AIMDD Note to the reader: Due to technical issues, please disregard the document displayed from 7 September 2023 until 8 September 2023. | in_force |
| 指南 | MDCG 2020-4 | Guidance on temporary extraordinary measures related to medical device notified body audits during COVID-19 quarantine orders and travel restrictions | in_force |
| 指南 | MDCG 2020-5 | Guidance on clinical evaluation – Equivalence | in_force |
| 指南 | MDCG 2020-7 | Guidance on PMCF plan template | in_force |
| 指南 | MDCG 2020-8 | Guidance on PMCF evaluation report template | in_force |
| 指南 | MDCG 2020-9 | Regulatory requirements for ventilators and related accessories | in_force |
| 指南 | MDCG 2021-1 rev.1 | Guidance on harmonised administrative practices and alternative technical solutions until EUDAMED is fully functional | in_force |
| 指南 | MDCG 2021-10 | The status of Appendixes E-I of IMDRF N48 under the EU regulatory framework for medical devices | in_force |
| 指南 | MDCG 2021-11 | Guidance on Implant Card – Device types | in_force |
| 指南 | MDCG 2021-12 rev.2 | FAQ on the European Medical Device Nomenclature ( EMDN ) | in_force |
| 指南 | MDCG 2021-13 rev.1 | Questions and answers on obligations and related rules for the registration in EUDAMED of actors other than manufacturers, authorised representatives and importers subject to the obligations of Article 31 MDR and Article 28 IVDR | in_force |
| 指南 | MDCG 2021-14 | Explanatory note on IVDR codes | in_force |
| 指南 | MDCG 2021-15 rev.1 | Application form to be submitted by a conformity assessment body when applying for designation as notified body under the medical devices regulation ( MDR ) | in_force |
| 指南 | MDCG 2021-15/MDCG 2024-7 Annex | Annex to Application Form & PAR Template MDR (List of documents) | in_force |
| 指南 | MDCG 2021-16 rev.1 | Application form to be submitted by a conformity assessment body when applying for designation as notified body under the in vitro diagnostic devices regulation ( IVDR ) | in_force |
| 指南 | MDCG 2021-16/MDCG 2024-8 Annex | Annex to Application Form & PAR Template IVDR (List of documents) | in_force |
| 指南 | MDCG 2021-17 | Applied-for scope of designation and notification of a conformity assessment body – Regulation (EU) 2017/745 (MDR) | in_force |
| 指南 | MDCG 2021-18 | Applied-for scope of designation and notification of a conformity assessment body – Regulation (EU) 2017/746 (IVDR) | in_force |
| 指南 | MDCG 2021-19 | Guidance note integration of the UDI within an organisation’s quality management system | in_force |
| 指南 | MDCG 2021-2 | Guidance on state of the art of COVID-19 rapid antibody tests | in_force |
| 指南 | MDCG 2021-20 | Instructions for generating CIV-ID for MDR Clinical Investigations | in_force |
| 指南 | MDCG 2021-21 rev.1 | Guidance on performance evaluation of SARS-CoV-2 in vitro diagnostic medical devices | in_force |
| 指南 | MDCG 2021-22 rev.1 | Clarification on “first certification for that type of device” and corresponding procedures to be followed by notified bodies, in context of the consultation of the expert panel referred to in Article 48(6) of Regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2021-23 | Guidance for notified bodies, distributors and importers on certification activities in accordance with Article 16(4) of Regulation (EU) 2017/745 and Regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2021-24 rev.1 | Guidance on classification of medical devices | in_force |
| 指南 | MDCG 2021-25 rev.1 | Application of MDR requirements to " legacy devices " and to devices placed on the market prior to 26 May 2021 in accordance with Directives 90/385/EEC or 93/42/EEC | in_force |
| 指南 | MDCG 2021-26 | Q&A on repackaging & relabelling activities under Article 16 of Regulation (EU) 2017/745 and Regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2021-27 - rev.1 | Questions and Answers on Articles 13 & 14 of Regulation (EU) 2017/745 and Regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2021-28 | Substantial modification of clinical investigation under Medical Device Regulation | in_force |
| 指南 | MDCG 2021-3 | Questions and Answers on Custom-Made Devices | in_force |
| 指南 | MDCG 2021-4 rev.1 | Application of transitional provisions for certification of class D in vitro diagnostic medical devices according to Regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2021-5 rev.1 | Guidance on standardisation for medical devices | in_force |
| 指南 | MDCG 2021-5 rev.1 - Appendix | Transition to the "EU REP" symbol in EN ISO 15223-1 | in_force |
| 指南 | MDCG 2021-6 - rev.1 | Regulation (EU) 2017/745 – Questions & Answers regarding clinical investigation | in_force |
| 指南 | MDCG 2021-7 | Notice to manufacturers and authorised representatives on the impact of genetic variants on SARS-COV-2 in vitro diagnostic medical devices | in_force |
| 指南 | MDCG 2021-8 | Clinical investigation application/notification documents | in_force |
| 指南 | MDCG 2022-1 | Notice to 3rd country manufacturers of SARS-CoV-2 in vitro diagnostic medical devices | in_force |
| 指南 | MDCG 2022-10 | Q&A on the interface between Regulation (EU) 536/2014 on clinical trials for medicinal products for human use (CTR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR) | in_force |
| 指南 | MDCG 2022-11 - rev.1 | MDCG Position Paper: Notice to manufacturers to ensure timely compliance with MDR and IVDR requirements | in_force |
| 指南 | MDCG 2022-12 | Guidance on harmonised administrative practices and alternative technical solutions until Eudamed is fully functional (for Regulation (EU) 2017/746 on in vitro diagnostic medical devices) | in_force |
| 指南 | MDCG 2022-13 rev.1 | Designation, re-assessment and notification of conformity assessment bodies and notified bodies | in_force |
| 指南 | MDCG 2022-14 | Transition to the MDR and IVDR - Notified body capacity and availability of medical devices and IVDs | in_force |
| 指南 | MDCG 2022-15 | Guidance on appropriate surveillance regarding the transitional provisions under Article 110 of the IVDR with regard to devices covered by certificates according to the IVDD | in_force |
| 指南 | MDCG 2022-16 | Guidance on Authorised Representatives Regulation (EU) 2017/745 and Regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2022-17 | MDCG position paper on "hybrid audits" | in_force |
| 指南 | MDCG 2022-18 | MDCG Position Paper on the application of Article 97 MDR to legacy devices for which the MDD or AIMDD certificate expires before the issuance of a MDR certificate | in_force |
| 指南 | MDCG 2022-18 ADD.1 | MDCG Position Paper on the application of Article 97 MDR to legacy devices for which the MDD or AIMDD certificate expires before the issuance of a MDR certificate - Addendum 1 | in_force |
| 指南 | MDCG 2022-19 | Performance study application/notification documents under Regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2022-2 | Guidance on general principles of clinical evidence for In Vitro Diagnostic medical devices (IVDs) | in_force |
| 指南 | MDCG 2022-20 | Substantial modification of performance study under Regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2022-21 | Guidance on Periodic Safety Update Report (PSUR) according to Regulation (EU) 2017/745 | in_force |
| 指南 | MDCG 2022-3 rev.1 | Verification of manufactured class D IVDs by notified bodies | in_force |
| 指南 | MDCG 2022-4 rev.2 | Guidance on appropriate surveillance regarding the transitional provisions under Article 120 of the MDR with regard to devices covered by certificates according to the MDD or the AIMDD | in_force |
| 指南 | MDCG 2022-5 rev.1 | Guidance on borderline between medical devices and medicinal products under Regulation (EU) 2017/745 on medical devices | in_force |
| 指南 | MDCG 2022-6 | Guidance on significant changes regarding the transitional provision under Article 110(3) of the IVDR | in_force |
| 指南 | MDCG 2022-7 | Q&A on the Unique Device Identification system under Regulation (EU) 2017/745 and Regulation (EU) | in_force |
| 指南 | MDCG 2022-8 | Regulation (EU) 2017/746 - application of IVDR requirements to ‘legacy devices’ and to devices placed on the market prior to 26 May 2022 in accordance with Directive 98/79/EC | in_force |
| 指南 | MDCG 2022-9 rev.1 | Summary of safety and performance template | in_force |
| 指南 | MDCG 2023-1 | Guidance on the health institution exemption under Article 5(5) of Regulation (EU) 2017/745 and Regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2023-2 | List of Standard Fees | in_force |
| 指南 | MDCG 2023-3 rev.2 | Questions and Answers on vigilance terms and concepts as outlined in the Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2023-4 | Medical Device Software (MDSW) – Hardware combinations Guidance on MDSW intended to work in combination with hardware or hardware components | in_force |
| 指南 | MDCG 2023-5 | Guidance on qualification and classification of Annex XVI products - A guide for manufacturers and notified bodies | in_force |
| 指南 | MDCG 2023-6 | Guidance on demonstration of equivalence for Annex XVI products - A guide for manufacturers and notified bodies | in_force |
| 指南 | MDCG 2023-7 | Guidance on exemptions from the requirement to perform clinical investigations pursuant to Article 61(4)-(6) MDR and on sufficient levels of access’ to data needed to justify claims of equivalence | in_force |
| 指南 | MDCG 2024-1 | Device Specific Vigilance Guidance (DSVG) Template | in_force |
| 指南 | MDCG 2024-1-1 | DSVG 01 on Cardiac ablation | in_force |
| 指南 | MDCG 2024-1-2 | DSVG 02 on Coronary stents | in_force |
| 指南 | MDCG 2024-1-3 | DSVG 03 on Cardiac implantable electronic devices (CIEDs) | in_force |
| 指南 | MDCG 2024-1-4 | DSVG 04 on Breast implants | in_force |
| 指南 | MDCG 2024-1-5 | DSVG 05 on Urogynaecological Surgical Mesh Implants used for Pelvic Organ Prolapse repair and Stress Urinary Incontinence | in_force |
| 指南 | MDCG 2024-10 | Clinical evaluation of orphan medical devices | in_force |
| 指南 | MDCG 2024-11 | Guidance on qualification of in vitro diagnostic medical devices | in_force |
| 指南 | MDCG 2024-12 | Corrective and preventive action (CAPA) plan assessment: guidance and templates for conformity assessment bodies, notified bodies, designating authorities, and joint assessment teams | in_force |
| 指南 | MDCG 2024-12 Annex I Form | Annex I: Template CAPA plan and assessment thereon | in_force |
| 指南 | MDCG 2024-12 Annex II Form | Annex II: Template JAT review of the CAPA and the DA's opinion | in_force |
| 指南 | MDCG 2024-13 | Regulatory status of ethylene oxide (EtO) intended for the sterilisation of medical devices | in_force |
| 指南 | MDCG 2024-14 - rev.1 | Guidance on the implementation of the Master UDI-DI solution for contact lenses | in_force |
| 指南 | MDCG 2024-15 | Guidance on the publication of the clinical investigation reports and their summaries in the absence of EUDAMED | in_force |
| 指南 | MDCG 2024-16 | Manufacturer Information Form on Interruption or Discontinuation of Supply of certain medical devices and certain in vitro diagnostic medical devices | in_force |
| 指南 | MDCG 2024-16 Annex | Device Identification table | in_force |
| 指南 | MDCG 2024-2 rev.1 | Procedures for the updates of the EMDN | in_force |
| 指南 | MDCG 2024-3 | Guidance on content of the Clinical Investigation Plan for clinical investigations of medical devices | in_force |
| 指南 | MDCG 2024-3 Appendix A | Clinical Investigation Plan Synopsis Template | in_force |
| 指南 | MDCG 2024-4 | Safety reporting in performance studies of in vitro diagnostic medical devices under Regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2024-4 Appendix | Appendix – Performance Study Summary Safety Reporting Form | in_force |
| 指南 | MDCG 2024-5 | Guidance on the Investigator’s Brochure content | in_force |
| 指南 | MDCG 2024-5 Appendix A | Appendix A of the MDCG 2024-5 | in_force |
| 指南 | MDCG 2024-6 | Preliminary re-assessment review (PRAR) form template (MDR) | in_force |
| 指南 | MDCG 2024-7 rev.1 | Preliminary assessment review (PAR) form template (MDR) | in_force |
| 指南 | MDCG 2024-8 rev.1 | Preliminary assessment review (PAR) form template (IVDR) | in_force |
| 指南 | MDCG 2024-9 | Preliminary re-assessment review (PRAR) form template (IVDR) | in_force |
| 指南 | MDCG 2025-1 | EMDN Ad hoc procedure | in_force |
| 指南 | MDCG 2025-2 | Summary of EMDN 2024 Submissions and outcome of annual revision | in_force |
| 指南 | MDCG 2025-3 | 2024-2025 Annual Revision Change Log | in_force |
| 指南 | MDCG 2025-4 | Guidance on the safe making available of medical device software (MDSW) apps on online platforms | in_force |
| 指南 | MDCG 2025-5 | Questions & Answers regarding performance studies of in vitro diagnostic medical devices under regulation (EU) 2017/746 | in_force |
| 指南 | MDCG 2025-6 | FAQ on Interplay between the Medical Devices Regulation (MDR) & In vitro Diagnostic Medical Devices Regulation (IVDR) and the Artificial Intelligence Act (AIA) | in_force |
| 指南 | MDCG 2025-7 | MDCG Position Paper: Timelines of the implementation of ‘Master UDI-DI’ to contact lenses and spectacle frames, spectacle lenses and ready-to-wear reading spectacles | in_force |
| 指南 | MDCG 2025-8 - rev.1 | Guidance on the implementation of the Master UDI-DI solution for spectacle frames, spectacle lenses and ready-to-wear reading spectacles | in_force |
| 指南 | MDCG 2025-9 | Guidance on Breakthrough Devices (BtX) under Regulations 2017/745 & 2017/746 Note: Pilot to roll-out the guidance is expected to be launched in Q2 2026 | in_force |
| 指南 | MDCG 2025–10 | Guidance on post-market surveillance of medical devices and in vitro diagnostic medical devices | in_force |
| 指南 | MDCG 2026-1 | Summary of EMDN 2025 Submissions and outcome of annual revision | in_force |
| 指南 | MDCG 2026-2 | 2025-2026 Annual Revision Change Log | in_force |
| 指南 | MDCG 2026-3 | 2026 EMDN Version History | in_force |
| 指南 | MDCG 2026-4 | MDCG Position Paper: Management of SS(C)P in EUDAMED after mandatory use | in_force |
| 指南 | MDCG 2026-5 | Position Paper: UDI assignment between manufacturers and distributors | in_force |
| 指南 | MDR/IVDR Language requirements | Overview of language requirements for manufacturers of medical devices for the information and instructions that accompany a device in a specific country | in_force |
| 指南 | NBOG BPG 2017-2 | Best practice guidance on the information required for personnel involved in conformity assessment | in_force |
| 指南 | NBOG F 2017-7 | Review of qualification for the authorisation of personnel (MDR) | in_force |
| 指南 | NBOG F 2017-8 | Review of qualification for the authorisation of personnel (IVDR) | in_force |
| 指南 | Q&A | Q&A on practical aspects related to the implementation of the extended transitional period provided for in the IVDR, as amended by Regulation (EU) 2024/1860 | in_force |
| 指南 | Q&A rev.2 | Q&A on practical aspects related to the implementation of Regulation (EU) 2023/607 - Extension of the MDR transitional period and removal of the “sell off” periods | in_force |
| 指南 | SCHEER guidelines | Update on the guidelines on the benefit-risk assessment of the presence of phthalates in certain medical devices covering phthalates which are carcinogenic, mutagenic, toxic to reproduction (CMR) or have endocrine-disrupting (ED) properties | in_force |
| 法律 | 31990L0385 | Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices | repealed |
| 法律 | 31993L0042 | Council Directive 93/42/EEC of 14 June 1993 concerning medical devices | repealed |
| 法律 | 32017R0745 | Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (Text with EEA relevance) | in_force |
| 法律 | 32017R0746 | Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU (Text with EEA relevance) | in_force |
| 法规/条例 | 32017R2185 | Commission Implementing Regulation (EU) 2017/2185 of 23 November 2017 on the list of codes and corresponding types of devices for the purpose of specifying the scope of the designation as notified bodies in the field of medical devices under Regulation (EU) 2017/745 of the European Parliament and of the Council and in vitro diagnostic medical devices under Regulation (EU) 2017/746 of the European Parliament and of the Council (Text with EEA relevance) | in_force |
| 法规/条例 | 32022R0112 | Regulation (EU) 2022/112 of the European Parliament and of the Council of 25 January 2022 amending Regulation (EU) 2017/746 as regards transitional provisions for certain in vitro diagnostic medical devices and the deferred application of conditions for in-house devices (Text with EEA relevance) | in_force |
| 法规/条例 | 32023R0607 | Regulation (EU) 2023/607 of the European Parliament and of the Council of 15 March 2023 amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards the transitional provisions for certain medical devices and in vitro diagnostic medical devices (Text with EEA relevance) | in_force |
| 法规/条例 | 32025R2526 | Commission Implementing Regulation (EU) 2025/2526 of 16 December 2025 amending Implementing Regulation (EU) 2023/2713 to correct the designation of an EU reference laboratory and to designate European Union reference laboratories for in vitro diagnostic medical devices intended for detection or quantification of markers of parasite infection and detection of blood grouping markers | in_force |