Medical Devices Regulations 2002

This document cites

• National Health Service (Scotland) Act 1978
• European Communities Act 1972
• Finance Act 1973
• Consumer Protection Act 1987
• European Communities (Designation) (No. 3) Order 1991



See all quotations

• Active Implantable Medical Devices Regulations 1992
• The Medicines (Products for Human Use) (Fees) Regulations 2016
• Medical Devices Fees (Amendment) Regulations 1997
• Units of Measurement Regulations 1986
• Personal Protective Equipment at Work Regulations 1992
• Medical Devices Regulations 1994
• Medical Devices Fees Regulations 1995
• Clinical Thermometers (EEC Requirements) Regulations 1993
• European Communities (Designation) (No. 3) Order 1993
• Active Implantable Medical Devices (Amendment and Transitional Provisions) Regulations 1995
• Directive 2001/83/EC of the European Parliament and of the Council of 6 November 2001 on the Community code relating to medicinal products for human use
• Council Directive 67/548/EEC of 27 June 1967 on the approximation of laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances
• Directive 98/48/EC of the European Parliament and of the Council of 20 July 1998 amending Directive 98/34/EC laying down a procedure for the provision of information in the field of technical standards and regulations
• Council Directive 88/379/EEC of 7 June 1988 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the classification, packaging and labelling of dangerous preparations
• Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
• Council Directive 90/385/EEC of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices
• Council Directive 80/181/EEC of 20 December 1979 on the approximation of the laws of the Member States relating to units of measurement and on the repeal of Directive 71/354/EEC