FAQ on Interplay between the Medical Devices Regulation (MDR) & In vitro Diagnostic Medical Devices Regulation (IVDR) and the Artificial Intelligence Act (AIA)

European Union · Last verified: 2026-09-08

Number

MDCG 2025-6

Type

Guidance

Issuer

Medical Device Coordination Group (MDCG)

Status

in_force

Authority

欧盟委员会 / MDCG

What this covers

MDCG 指南文件，属「New technologies」专题，委员会指南清单页标注的发布时间为 June 2025；内容为「FAQ on Interplay between the Medical Devices Regulation (MDR) & In vitro Diagnostic Medical Devices Regulation (IVDR) and the Artificial Intelligence Act (AIA)」。此类文件无强制法律效力，但代表成员国主管当局与公告机构对 MDR/IVDR 的共同解释口径。注意 effective 填的是发布月份（日补 01），不是法律生效日。

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