Menu
0
Total price
0 €
PRICES include / exclude VAT
>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)
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)

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).

Format
Availability
Price and currency
Španělsky PDF
Immediate download
Printable
91.24 €
Španělsky Hardcopy
In stock
91.24 €
Anglicky PDF
Immediate download
Printable
109.49 €
Anglicky Hardcopy
In stock
109.49 €
Označení normy:UNE EN ISO 18113-2:2025
Počet stran:25
Vydáno:2025-01-22
Status:Norma
Počet stran (Španělsky):28
DESCRIPTION

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.

Categories: