NA 176
DIN Standards Committee Health Technologies
DIN EN ISO 18113-3 [Pre-order] references following documents:
| Document number | Edition | Title |
|---|---|---|
| DIN EN ISO 18113-2 | 2024-10 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022); German version EN ISO 18113-2:2024 More |
| DIN EN 61010-1 ; VDE 0411-1:2023-08 | 2023-08 | Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: General requirements (IEC 66/769/CD:2022); Text in German and English More |
| ISO 15198 | 2004-07 | Clinical laboratory medicine - In vitro diagnostic medical devices - Validation of user quality control procedures by the manufacturer More |
| ISO 17511 | 2020-04 | In vitro diagnostic medical devices - Requirements for establishing metrological traceability of values assigned to calibrators, trueness control materials and human samples More |
| ISO 18113-2 | 2022-10 | In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use More |
| ISO/IEC 15415 | 2011-12 | Information technology - Automatic identification and data capture techniques - Bar code symbol print quality test specification - Two-dimensional symbols More |
