Regulations on Customized Medical Devices (Trial)

On:
In: declaration, Medicine/medical devices, NMPA, Regulation/Rule/Measure
On July 4, the National Medical Products Administration and the National Health Commission issued the Regulations on the Supervision and Administration of Customized Medical Devices (Trial), which came into effect on January 1, 2020. Personalized medical devices refer to medical devices designed and manufactured according to the clinical needs of authorized medical personnel in medical institutions, which meet the individual requirements. They are divided into customized medical devices and patient-matched medical devices. The customized medical devices shall be put on record before going on the market. Manufacturing enterprises of customized medical devices and medical institutions shall jointly act as archivists.Read More →

Thank you for your interests/registration! For complete and full access to our platform, please contact us to subscribe as a paid-up member. The annual fee is ＄5,500 Best! Paolo yue Email: yuefeng7832@hotmail.com Cell: 008613501397114

Existing Users Log In
   
New User Registration
*Required field

Related posts:

  1. Measures for clinical use of medical devices
  2. Rules for Unique Identification of Medical Devices
  3. Measures for registration and filing of medical devices
  4. Electronic registration certificate of medical devices
  5. Approval of domestic class III and imported medical devices
  6. Measures for registration and filing of medical devices
  7. NMPA adjusts production license for imported medical devices
  8. Class III medical devices subject to clinical trials 2020
  9. Regulations on self-inspection of medical device
  10. National Drugs Catalogue of Basic Medical, labor Injury and Maternity Insurance