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Homepage>UNE standards>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)
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in stockReleased: 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)

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English PDF
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125.40 EUR
English Hardcopy
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125.40 EUR
Spanish PDF
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104.50 EUR
Spanish Hardcopy
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Standard number:UNE EN ISO 18113-1:2012
Pages:60
Released:2012-02-22
Status:Standard
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:

  • 11.100.10
  • 11.100.99
Categories:
UNE standards
11.100.10 In vitro diagnostic test systems
11.100.99 Other standards related to laboratory medicine
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