New labelling and MDEL requirements for medical devices authorized under interim orders on September 1, 2021 (French, HTML)

View metadata and access the original French HTML file: New labelling and MDEL requirements for medical devices authorized under interim orders on September 1, 2021.

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Publisher-reported update

2023-02-27

Labels of IO-authorized devices must be, at a minimum, in either English or French. There are also several additional requirements (for example, bilingual labelling) depending on whether the device is to be sold to the general public.

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