http://www.legislation.gov.uk/uksi/2002/618/regulation/8/made
The Medical Devices Regulations 2002
Consumer protection
European Union
European Parliament
King's Printer of Acts of Parliament
2015-04-27
CONSUMER PROTECTION
These Regulations contain the legislative measures necessary for the implementation of three European Community Directives: Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, as amended; Council Directive 93/42/EEC concerning medical devices, as amended; and Directive 98/79/EC of the European Parliament and of the Council on in vitro diagnostic medical devices (“the Medical Devices Directives”). They also contain the legislative measures necessary for the implementation, in relation to medical devices, of the agreements on mutual recognition between the European Community and Australia, New Zealand, Canada and the United States of America—and of the Association Agreement between the European Communities, and their Member States, and Hungary.
The Medical Devices Regulations 2002
Pt. 8
The Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
reg. 10
reg. 1(1)
The Medical Devices Regulations 2002
Pt. 9
The Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
reg. 11
reg. 1(1)
The Medical Devices Regulations 2002
reg. 4D(10)(b)
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 2(3)(a)
reg. 1
The Medical Devices Regulations 2002
reg. 4E(7)
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 2(3)(b)
reg. 1
The Medical Devices Regulations 2002
reg. 6(d)
The Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
reg. 4(2)
reg. 1(1)
The Medical Devices Regulations 2002
reg. 33(1)(c)
The Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
reg. 6(2)(a)
reg. 1(1)
The Medical Devices Regulations 2002
reg. 33(2)(c)
The Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
reg. 6(2)(b)
reg. 1(1)
The Medical Devices Regulations 2002
reg. 75(3)
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 9(2)(a)
reg. 1
The Medical Devices Regulations 2002
reg. 75(7)
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 9(2)(b)
reg. 1
The Medical Devices Regulations 2002
reg. 93(4)
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 9(3)
reg. 1
The Medical Devices Regulations 2002
reg. 119(6)
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 9(4)
reg. 1
The Medical Devices Regulations 2002
reg. 124(5)
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 9(5)
reg. 1
The Medical Devices Regulations 2002
reg. 149(5)(e)
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 10(2)
reg. 1
The Medical Devices Regulations 2002
reg. 158(1)
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 10(3)(a)
reg. 1
The Medical Devices Regulations 2002
reg. 158(3)
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 10(3)(b)
reg. 1
The Medical Devices Regulations 2002
Sch. 19
para. 5
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 11(2)(a)
reg. 1
The Medical Devices Regulations 2002
Sch. 19
para. 5
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 11(2)(b)
reg. 1
The Medical Devices Regulations 2002
Sch. 24 para. 1(7) heading
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 11(3)(a)
reg. 1
The Medical Devices Regulations 2002
Sch. 24
para. 1(7)
The Human Medicines and Medical Devices (Amendment etc.) (EU Exit) Regulations 2019
Sch. 2
para. 11(3)(b)
reg. 1
The Medical Devices Regulations 2002
reg. 60A-60C
Medicines and Medical Devices Act 2021
Sch. 3
para. 1
s. 50(3)
The Medical Devices Regulations 2002
reg. 60A
Medicines and Medical Devices Act 2021
Sch. 2
para. 4
s. 50(3)
The Medical Devices Regulations 2002
reg. 60A
Medicines and Medical Devices Act 2021
Sch. 2
para. 5(2)
s. 50(3)
The Medical Devices Regulations 2002
Sch. 3
Medicines and Medical Devices Act 2021
Sch. 3
para. 2
s. 50(3)
PART IIGeneral Medical Devices
Essential requirements for general medical devices8
1
Subject to regulation 12, no person shall place on the market or put into service a relevant device unless that device meets those essential requirements set out in Annex I which apply to it.
2
Subject to regulation 12, no person shall supply a relevant device—
a
if that supply is also a placing on the market or putting into service of that device; or
b
in circumstances where that device has been placed on the market or put into service,
unless that device meets those essential requirements set out in Annex I which apply to it.