| 1. | Citation and commencement |
| 2. | Interpretation |
| 3. | Application of Regulations |
| 4. | Classification of devices |
| 5. | Essential requirements for devices |
| 6. | CE marking |
| 7. | Procedure for affixing CE marking for Class I devices |
| 8. | Procedure for affixing CE marking for Class IIa devices |
| 9. | Procedure for affixing CE marking for Class IIb devices |
| 10. | Procedure for affixing CE marking for Class III devices |
| 11. | Procedure for systems and procedure packs, and devices to be sterilised before use |
| 12. | General provisions relating to conformity assessment procedures |
| 13. | Obligations of persons other than manufacturers |
| 14. | Registration of persons placing devices on the market |
| 15. | Custom-made devices |
| 16. | Clinical investigations |
| 17. | Notified bodies |
| 18. | Prohibition on supply etc. |
| 19. | Enforcement etc. |
| 20. | Centralised system of records etc. |
| 21. | Fees |
| 22. | Transitional provisions |
| 23. | Notification of decisions etc. |
| 24. | Amendment of Schedule 1 to the Provision and Use of Work Equipment Regulations 1992 |
| 25. | Substitution for Schedule 1 to the Personal Protective Equipment at Work Regulations 1992 |
| 26. | Amendment of the Clinical Thermometers (EEC Requirements) Regulations 1993 |
| 27. | Amendment of the Electro-medical Equipment (EEC Requirements) Regulations 1988 |
