Standard

NS-EN ISO 22442-2:2020

Publisert

Rettelser og tillegg kjøpes separat.

Språk
Tjenester

Omfang

This document specifies requirements for controls on the sourcing, collection, and handling (which includes storage and transport) of animals and tissues for the manufacture of medical devices utilizing materials of animal origin other than in vitro diagnostic medical devices. It applies where required by the risk management process as described in ISO 22442‑1. NOTE Selective sourcing is especially important for transmissible spongiform encephalopathy (TSE) risk management, i.e. when utilising animal tissue and/or their derivative originating from bovine, ovine and caprine species, deer, elk, mink or cats. This document does not cover the utilization of human tissues in medical devices. This document does not specify a quality management system for the control of all stages of production of medical devices.

Dokumentinformasjon

  • Standard fra SN
  • Publisert:
  • Utgave: 2020-12
  • Versjon: 1
  • Varetype: NAT
  • Products.Specs.pages
  • ICS 11.100.20
  • National Committee SN/K 115

Referanser i lov

EU lov:
Lov referanseRestriksjoner
93/42/EEC

Produktrelasjon

Produkt livssyklus