Cena s DPH / bez DPH
sklademVydáno: 2025-01-22
UNE EN ISO 18113-2:2025
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022)
Productos sanitarios para diagnóstico in vitro. Información proporcionada por el fabricante (etiquetado). Parte 2: Reactivos para diagnóstico in vitro para uso profesional. (ISO 18113-2:2022).
Formát
Dostupnost
Cena a měna
Španělsky PDF
K okamžitému stažení
Tisknutelné
2222 Kč
Španělsky Tisk
Skladem
2222 Kč
Anglicky PDF
K okamžitému stažení
Tisknutelné
2666 Kč
Anglicky Tisk
Skladem
2666 Kč
| Označení normy: | UNE EN ISO 18113-2:2025 |
| Počet stran: | 25 |
| Vydáno: | 2025-01-22 |
| Status: | Norma |
| Počet stran (Španělsky): | 28 |
Popis
UNE EN ISO 18113-2:2025
This document specifies requirements for information supplied by the manufacturer of IVD reagents, calibrators and controls intended for professional use. This document can also be applied to accessories. This document applies to the labels for outer and immediate containers and to the instructions for use. This document does not apply to: a) IVD instruments or equipment; b) IVD reagents for self-testing.
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