Skip to main content
QMSQMS
QMS
  • Welcome to your QMS
  • Quality Manual
  • Procedures
  • Records
  • TF_Legit.Health_Plus
  • Licenses and accreditations
  • External documentation
    • 01 ES πŸ‡ͺπŸ‡Έ regulations
    • 02 US πŸ‡ΊπŸ‡Έ CFR FDA
    • 03_Clinical studies
    • 04 EU πŸ‡ͺπŸ‡Ί Medical devices
    • 05_GP-004 Vigilance system
    • 06_Machine learning
    • 07 Quality regulations
    • 08 MX πŸ‡²πŸ‡½ regulations
    • 09 Pharmacy
    • 10 Other
    • 11 UK πŸ‡¬πŸ‡§ Medical devices
      • 11_01_UK Medical devices regulations 2002
    • 12 EU πŸ‡ͺπŸ‡Ί AI Act
  • External documentation
  • 11 UK πŸ‡¬πŸ‡§ Medical devices
  • 11_01_UK Medical devices regulations 2002

11_01_UK Medical devices regulations 2002

The link to the most updated version of the UK medical device regulation is this one.

The PDF version is only available for the first version of the regulation that is dated back to 2002.

Previous
11 UK πŸ‡¬πŸ‡§ Medical devices
Next
12 EU πŸ‡ͺπŸ‡Ί AI Act
All the information contained in this QMS is confidential. The recipient agrees not to transmit or reproduce the information, neither by himself nor by third parties, through whichever means, without obtaining the prior written permission of Legit.Health (AI LABS GROUP S.L.)