Menu
0
Total price
0 €
PRICES include / exclude VAT
Homepage>UNE EN ISO 18113-1:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
sklademVydáno: 2012-02-22
UNE EN ISO 18113-1:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)

UNE EN ISO 18113-1:2012

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)

Productos sanitarios para diagnóstico in vitro. Información proporcionada por el fabricante (etiquetado). Parte 1: Términos, definiciones y requisitos generales. (ISO 18113-1:2009)

Format
Availability
Price and currency
Anglicky PDF
Immediate download
136.80 €
Anglicky Hardcopy
In stock
136.80 €
Španělsky PDF
Immediate download
114.00 €
Španělsky Hardcopy
In stock
114.00 €
Označení normy:UNE EN ISO 18113-1:2012
Počet stran:60
Vydáno:2012-02-22
Status:Norma
DESCRIPTION

This standard UNE EN ISO 18113-1:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009) is classified in these ICS categories:

  • 11.100.99
  • 11.100.10
Categories: