MDR meaning

MDR, or Medical Device Regulation, is a set of regulatory requirements for medical devices in the European Union.


MDR definitions

Word backwards RDM
Part of speech MDR is an initialism and does not represent a specific part of speech.
Syllabic division MDR has one syllable: MDR
Plural The plural form of MDR is MDRs.
Total letters 3
Vogais (0)
Consonants (3) m,d,r

Medical Device Regulation (MDR) is a set of regulations that govern the manufacturing, distribution, and sale of medical devices within the European Union. These regulations aim to ensure that all medical devices meet high standards of quality, safety, and performance.

Key Components of MDR

MDR covers a wide range of topics related to medical devices, including classification, conformity assessment, clinical evaluation, post-market surveillance, and labeling. It also includes provisions for increased transparency and traceability of devices throughout their lifecycle.

Impact on Medical Device Industry

The implementation of MDR has had a significant impact on the medical device industry, requiring manufacturers to make substantial changes to comply with the new regulations. This has led to increased costs and longer timelines for bringing products to market.

Benefits of MDR

Despite the challenges it presents, MDR ultimately benefits patients and healthcare professionals by ensuring that medical devices are safe, effective, and of high quality. It also helps to improve patient outcomes and enhance public health.

Transition to MDR

Manufacturers of medical devices need to transition to the new MDR by May 26, 2021, to continue selling their products in the European market. This transition involves updating technical documentation, conducting new clinical evaluations, and implementing post-market surveillance systems.

Enforcement of MDR

MDR is enforced by national competent authorities in each EU member state, who are responsible for ensuring compliance with the regulations. Non-compliance can result in serious consequences, including fines and restrictions on market access.

In conclusion, MDR plays a crucial role in ensuring the safety and effectiveness of medical devices in the European Union. By adhering to these regulations, manufacturers can contribute to improving healthcare outcomes and protecting patient well-being.


MDR Examples

  1. MDR stands for Minimum Device Requirements.
  2. The MDR of this software is compatible with Windows 10.
  3. Make sure to check the MDR before purchasing a new computer.
  4. The MDR for this game includes a minimum of 8GB RAM.
  5. Consult the MDR guidelines for recommended system specifications.
  6. Always meet the MDR to ensure optimal performance.
  7. The MDR for this application specifies a minimum processor speed of 2.0GHz.
  8. If your device meets the MDR, you should have no issues running the software.
  9. The MDR may vary depending on the complexity of the program.
  10. Before downloading any new software, be sure to review the MDR to avoid compatibility issues.


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  • Updated 23/04/2024 - 15:24:31