18 lines
514 B
Plaintext
18 lines
514 B
Plaintext
{{#set: Description=Core EU regulatory frameworks: MDR (EU 2017/745) and IVDR (EU 2017/746).}}
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Pages in this category relate to EU regulatory frameworks governing medical devices and in vitro diagnostic devices, including MDR (EU 2017/745) and IVDR (EU 2017/746).
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== Documents ==
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{{#ask: [[Category:EU Regulation]] [[Status::+]]
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| ?Document name = Name
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| ?Status = Status
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| ?Area of validity = Region
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| ?Version = Version
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| format=table
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| headers=show
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| limit=50
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| sort=Status
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}}
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[[Category:Themes and topics]]
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