General Medical Devices

United Kingdom · Last verified: 2026-09-08

Number

S.I. 2002/618 PART II

Type

Regulation

Issuer

Secretary of State (UK); administered by MHRA

Status

in_force

Authority

MHRA

What this covers

第二部分规范一般医疗器械（原 93/42/EEC 转化）的基本要求、分类、合格评定程序、UKCA/CE 标志与投放市场条件，以及定制器械和临床研究器械的处理。

Contains public sector information licensed under the Open Government Licence v3.0