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in stockReleased: 2024-10
DIN EN ISO 18113-1
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)
In-vitro-Diagnostika - Bereitstellung von Informationen durch den Hersteller (Kennzeichnung) - Teil 1: Begriffe und allgemeine Anforderungen (ISO 18113-1:2022)
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| Status: | Standard |
| Released: | 2024-10 |
| Standard number: | DIN EN ISO 18113-1 |
| Name: | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022) |
| Pages: | 68 |
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DIN EN ISO 18113-1
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DIN EN 14136
Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures
Use of external quality assessment schemes in the assessment of the performance of in vitro diagnostic examination procedures
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