Packaging for terminally sterilized medical devices - Re-usable sterilization containers for steam sterilizers conforming to EN 285. Requirements and test methods Ingestion-build-146508

Packaging for terminally sterilized medical devices - Re-usable sterilization containers for steam sterilizers conforming to EN 285. Requirements and test methods Ingestion-build-146508What is this standard about? This document specifies test methods and values for re usable containers used as sterile barrier systems that are intended to maintain sterility of terminally sterilized medical devices to the point of use. These containers are intended to be used in steam sterilizers conforming to EN 285. Other than the general requirements as specified in EN ISO 116071 and EN ISO 116072 this part of EN 868 specifies materials, test

Evaluation of results

— drag augers

BS ISO 5208:2008 Industrial valves

ISO 5834-2 assists you with minimum requirements and test methods for manufacturing and evaluation of moulded forms made from ultra-high-molecular-weight polyethylene for use in surgical plants

for use as a link bridge

Note: BS EN 707 does not apply to -

He is also a member of two ISO Technical Committees responsible for technical product documentation and dimensional and geometrical product specification and verification

yet are specifically adapted to the requirements of a particular application environment

While the recommendations given in this part of BS EN ISO 9241 apply to a wide range of available front-end technologies

networked systems have become common

— or semi-trailer mounted

and EN 928 especially considering the nature and use of IVD MDs