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ΕΛΟΤ EN ISO 22442-2 Ε3

Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020)

ΕΛΟΤ EN ISO 22442-2 Ε3

Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020)

48,00 €

Abstract

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.

Info

Publication Date

2021-01-27

Greek Title

Προϊόντα για ιατρική χρήση που χρησιμοποιούν ζωικούς ιστούς και παράγωγά τους - Μέρος 2: Έλεγχος προέλευσης, συλλογής και χειρισμού

English Title

Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020)

Standard Stage

Techincal Body

Y

Related Documents

EN ISO 22442-2:2020 - Identical
ISO 22442-2:2020 - Identical
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