Standard

NS-EN 556-1:2001

Tilbaketrukket

Merknad: Denne standarden har en ny utgave: NS-EN 556-1:2024

Forhåndsvisning

Rettelser og tillegg kjøpes separat.

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Omfang

This European Standard specifies the requirements for a terminally-sterilized medical device to be designated 'STERILE'. Part 2 of this European Standard specifies the requirements for an aseptically processed medical device to be designated "STERILE". NOTE For the purpose of the EU Directive(s) for medical devices (see Bibliography), designation of a medical device as 'STERILE' is only permissible when a validated sterilization process has been applied. Requirements for validation and routine control of processes for the sterilization of medical devices are specified in EN 550, EN 552, EN 554, EN ISO 14160 and EN ISO 14937.

Dokumentinformasjon

  • Standard fra SN
  • Publisert:
  • Tilbaketrukket:
  • Utgave: 2001-10
  • Versjon: 1
  • Varetype: NAT
  • ICS 11.080.01
  • National Committee CEN/TC 204

Referanser i lov

EU lov: 90/385/EEC, 93/42/EEC, 98/79/EC

Produktrelasjon

Produkt livssyklus