Document refs

This is the list of documents referenced in the Entries service.

All European Community legislation referenced and linked in Entries are their latest consolidated versions. Likewise, all guidance documents referenced are their latest revisions. We reserve a reasonable time for making updates when new versions are published. All referenced documents can be found from one of the following sources:

The EUR-Lex home page that contains the European Union legislation.

The European Commission medical devices growth sector Guidance page, home of the MEDDEV's, Consensus statements and Informative documents. Other guidelines, such as the Manual on Borderline can be found from the Specific areas of development on the same page.

The International Medical Device Regulators Forum home page.

  1. Medical Device Regulation (MDR) 2017/745
  2. In Vitro Diagnostic Medical Device Regulation (IVDR) 2017/746
  3. Medical Device Directive 93/42/EEC (MDD)
  4. Active Implantable Medical Device Directive 90/385/EEC (AIMDD)
  5. In Vitro Diagnostic Medical Device Directive 98/79/EC (IVDD)
  6. Directive 2003/12/EC on Reclassification of Breast implants
  7. Directive 2005/50/EC on Reclassification of Hip, Knee and Shoulder Joint Replacements
  8. Regulation 722/2012 on Active Implantable Medical Devices and Medical Devices Manufactured Utilising Tissues of Animal Origin
  9. Directive 2001/83/EC relating to Medicinal Products for Human Use
  10. Regulation 2309/93 on the Authorization and Supervision of Medicinal Products for Human and Veterinary Use
  11. Regulation 1394/2007 on Advanced Therapy Medicinal Products
  12. Directive 2004/23/EC on setting standards of quality and safety for the donation, procurement, testing, processing, preservation, storage and distribution of human tissues and cells
  13. Directive 89/686/EEC relating to Personal Protective Equipment (PPE)
  14. Regulation 528/2012 on Biocidal Products
  15. Regulation 1907/2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH)
  16. Directive 80/181/EEC on Units of Measurement
  17. Directive 2015/1535 on Information Society Services
  18. MEDDEV 2.1/1 (Apr 1994) Definitions of “medical devices”, “accessory” and “manufacturer”
  19. MEDDEV 2.1/2 (rev. 2, Apr 1994) Field of application of the AIMDD
  20. MEDDEV 2.1/3 (rev. 3, Dec 2009) Borderline products, drug-delivery products and medical devices incorporating, as an integral part, an ancillary medicinal substance or an ancillary human blood derivative
  21. MEDDEV 2.1/4 (Mar 1994) Interface with other directives – Electromagnetic Compatibility (EMC) and Personal Protective Equipment (PPE)
  22. MEDDEV 2.1/5 (Jun 1998) Medical devices with a measuring function
  23. MEDDEV 2.1/6 (Jul 2016) Qualification and classification of stand alone software
  24. MEDDEV 2.4/1 (rev. 9, Jun 2010) Classification of medical devices
  25. MEDDEV 2.14/1 (rev. 2, Jan 2012) IVD medical device borderline and classification issues
  26. MEDDEV 2.14/2 (rev. 1, Feb 2004) IVD medical devices - Research Use Only (RUO) products
  27. Manual on Borderline and Classification in the Community Regulatory Framework for Medical Devices (ver. 1.18, Dec 2017)
  28. Interpretative guide of the relation between the MDD and the PPE Directive (21 Aug 2009)
  29. Requirements guide for IVD kits measuring parameters which can be used for evaluating the risk of trisomy 21 (Dec 2006)
  30. Interpretative guide on Placing on the market of medical devices (16 Nov 2010)
  31. The ‘Blue Guide’ on the implementation of EU products rules 2016
  32. GHTF: Principles of In Vitro Diagnostic (IVD) Medical Devices Classification (SG1(PD)/N045R12) (9 Feb 2007)
Share this Page