NF EN 556 + A1

NF EN 556 + A1

November 1998
Standard Cancelled

Sterilization of medical devices. Requirements for terminally-sterilized medical devices to be labelled "Sterile".

Le présent document spécifie les conditions que doivent remplir les dispositifs médi caux ayant subi une stérilisation terminale pour être étiquetés "Stérile" (à l'exception des dispositifs destinés au diagnostic in vitro.

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Main informations

Collections

National standards and national normative documents

Publication date

November 1998

Number of pages

8 p.

Reference

NF EN 556 + A1

ICS Codes

11.080.01   Sterilization and disinfection in general

Classification index

S98-107

Print number

1 - 04/11/1998

European kinship

EN 556:1994
Sumary
Sterilization of medical devices. Requirements for terminally-sterilized medical devices to be labelled "Sterile".

Le présent document spécifie les conditions que doivent remplir les dispositifs médi caux ayant subi une stérilisation terminale pour être étiquetés "Stérile" (à l'exception des dispositifs destinés au diagnostic in vitro.
Replaced standards (1)
NF EN 556
February 1995
Standard Cancelled
Sterilization of medical devices. Requirements for medical devices to be labelled "sterile".

Le présent document spécifie les conditions que doivent remplir les dispositifs médicaux ayant subi une stérilisation terminale pour être étiquetés "stérile" (à l'exception des dispositifs destinés au diagnostic in vitro).

Standard replaced by (1)
NF EN 556-1
February 2002
Standard Current
Sterilization of medical devices - Requirements for medical devices to be designated STERILE - Part 1 : requirements for terminally sterilized medical devices

Le présent document spécifie les exigences pour qu'un dispositif médical qui a subi une stérilisation terminale puisse être étiqueté "STÉRILE".

Table of contents
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  • Avant-propos
  • 1 Domaine d'application
  • 2 Références normatives
  • 3 Définitions
  • 4 Exigences
  • Annexe A (informative) Bibliographie
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