Category:EU Regulation: Difference between revisions
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{{#set: Description=Core EU regulatory frameworks: MDR (EU 2017/745) and IVDR (EU 2017/746).}} | |||
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). | 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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[[Category:Themes and topics]] | |||
Latest revision as of 16:39, 19 June 2026
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).
Documents
| Name | Status | Region | Version | |
|---|---|---|---|---|
| TestPage MDR | Medical Device Regulation (EU) 2017/745 | Current | EU | 2017/745, amended by 2023/607 |
| In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 | In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 | Current | EU | 2017/746, amended by 2022/1107 |
Pages in category "EU Regulation"
The following 2 pages are in this category, out of 2 total.
