Part III Active Implantable Medical Devices

1. 20Interpretation of Part III
2. 21Scope of Part III
3. 21ARegistration of persons placing active implantable medical devices on the market
4. 21BRegistration of persons placing active implantable medical devices on the market
5. 21CRequirement to appoint a UK responsible person for active implantable medical devices
6. 22Essential requirements for active implantable medical devices
7. 23Determining compliance of active implantable medical devices with relevant essential requirements
8. 24UK marking of active implantable medical devices
9. 24AUK(NI) indication: active implantable medical devices
10. 25UK marking of active implantable medical devices that come within the scope of this Part and other legislation
11. 26Exemptions from regulations 22 and 24
12. 27Procedures for affixing a UK marking to active implantable medical devices
13. 28Procedures for custom-made active implantable medical devices
14. 29Procedures for active implantable medical devices for clinical investigations
15. 30Manufacturers etc. and conformity assessment procedures for active implantable medical devices
16. 30AObligations in Part III which are met by complying with obligations in Directive 90/385
17. 31Approved bodies and the conformity assessment procedures for active implantable medical devices