In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)
DIN EN ISO 18113-1:2024-10

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)

Definitions*Instructions for use*In-vitro diagnostic*Laboratory medicine

€ 268.22Official print edition

Status

In Stock

Publisher

DIN

Year

2024

Standard No.

DIN EN ISO 18113-1:2024-10

1

Standard No: DIN EN ISO 18113-1:2024-10  |  Publisher: DIN