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Hlavní stránka>BS EN ISO 18113-1:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) Terms, definitions and general requirements
sklademVydáno: 2012-01-31
BS EN ISO 18113-1:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) Terms, definitions and general requirements

BS EN ISO 18113-1:2011

In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) Terms, definitions and general requirements

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Označení normy:BS EN ISO 18113-1:2011
Počet stran:62
Vydáno:2012-01-31
ISBN:978 0 580 77327 3
Status:Corrigendum
Popis

BS EN ISO 18113-1:2011


This standard BS EN ISO 18113-1:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) is classified in these ICS categories:
  • 11.100.10 In vitro diagnostic test systems

This part of ISO 18113 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.

This part of ISO 18113 does not address language requirements, since that is the domain of national laws and regulations.

This part of ISO 18113 does not apply to

  1. IVD devices for performance evaluation (e.g., for investigational use only),

  2. instrument marking,

  3. material safety data sheets.


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