PRICES include / exclude VAT
sklademVydáno: 2025-01-22
UNE EN ISO 18113-3:2025
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2022)
Productos sanitarios para diagnóstico in vitro. Información proporcionada por el fabricante (etiquetado). Parte 3: Instrumentos para diagnóstico in vitro para uso profesional. (ISO 18113-3:2022).
Format
Availability
Price and currency
Španělsky PDF
Immediate download
Printable
87.74 €
Španělsky Hardcopy
In stock
87.74 €
Anglicky PDF
Immediate download
Printable
105.29 €
Anglicky Hardcopy
In stock
105.29 €
| Označení normy: | UNE EN ISO 18113-3:2025 |
| Počet stran: | 23 |
| Vydáno: | 2025-01-22 |
| Status: | Norma |
| Počet stran (Španělsky): | 25 |
DESCRIPTION
UNE EN ISO 18113-3:2025
This document specifies requirements for information supplied by the manufacturer of IVD instruments intended for professional use. This document also applies to apparatus and equipment intended to be used with IVD instruments for professional use. This document can also be applied to accessories. This document does not apply to: a) instructions for instrument servicing or repair; b) IVD reagents, including calibrators and control materials for use in control of the reagent; c) IVD instruments for self-testing.
Categories:
