Reference:EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 Article 2 Paragraph 11: Difference between revisions
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| | |RefTags=TAG-00226-Kit-est ++ TAG-00244-Def-ini ++ TAG-00220-Inv-agn | ||
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| | |RefUnit=1.2.2 | ||
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| Module 1 β Unit 1.2.2 | |||
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! Tags | ! Tags | ||
| Β | | [[Glossary:TAG-00226-Kit-est|IVD kit]], [[Glossary:TAG-00244-Def-ini|Definition]], [[Glossary:TAG-00220-Inv-agn|IVD]] | ||
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Revision as of 17:29, 15 July 2026
| Document information | |
|---|---|
| Reference | EU Regulation (EU) 2017/746 - in vitro diagnostic medical devices 20-Mar-2023 |
| Validity area | EU |
| Scope(s) | IVD |
| Document name | Regulation (EU) 2017/746 - in vitro diagnostic medical devices |
| Version / Revision | 20-Mar-2023 |
| Status | Current |
| Document type | Legal act |
| Language(s) | EN |
| Description | Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU |
| Official source | Official link |
| Restricted access | No |
| Submitted by | Florian Adragna |
| Contributors | |
| Reference Details | |
|---|---|
| Module | Module 1 β Unit 1.2.2 |
| Scope | IVD |
| Document part | Article 2
Paragraph 11 |
| Language | EN |
| Original entry by | Florian Adragna |
| Contributors | |
| Tags | IVD kit, Definition, IVD |
| Comment | Definition of IVD kit |
Content
Definitions
(11) βkitβ means a set of components that are packaged together and intended to be used to perform a specific in vitro diagnostic examination, or a part thereof;
