Legacy devices

Information

Type

Miscellaneous

Regulated products

IVDMD, Medical Devices

Topics

Medical Device Industry

Last updated

February 28, 2024

Description

Regulation (EU) 2017/745, for medical devices, and Regulation (EU) 2017/746, for in vitro diagnostic medical devices, allow CE-marked devices under the previous directives to remain on the market in some particular cases.

Organization

Country / Region

Italy

License

Creative Commons Attribution 3.0

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