“medical device”

1. Consumer Protection Act 1987 Act
2. The Electromagnetic Compatibility Regulations 2005 SI 2 definitions
3. The Human Medicines Regulations 2012 SI
4. The Medical Devices Regulations 2002 SI 5 definitions
5. The Medicines (Products for Human Use-Fees) Regulations 2008 SI
6. The Nicotine Inhaling Products (Age of Sale and Proxy Purchasing) Regulations 2015 SI
7. The Pharmacy Order 2010 SI
8. The Private and Voluntary Health Care (England) Regulations 2001 SI
9. The Producer Responsibility Obligations (Packaging and Packaging Waste) Regulations 2024 SI
10. The Radio Equipment and Telecommunications Terminal Equipment Regulations 2000 SI
11. The Restriction of the Use of Certain Hazardous Substances in Electrical and Electronic Equipment Regulations 2012 SI 2 definitions
12. The Russia (Sanctions) (EU Exit) Regulations 2019 SI
13. The Tobacco and Related Products Regulations 2016 SI
14. Tobacco and Vapes Act 2026 Act 2 definitions
15. The Waste Electrical and Electronic Equipment Regulations 2013 SI

Definitions are taken from the instruments as published on zoomLaw, for guidance only. Check the instrument itself for its scope and any amendments.