Packaging for terminally sterilized medical devices - Requirements for materials, sterile barrier systems and packaging systemsWhat is this standard about? This part of ISO 11607 specifies the requirements and test methods for materials, preformed sterile barrier systems, sterile barrier systems and packaging systems that are intended to maintain sterility of terminally sterilized medical devices until the point of use. Who is this standard for? This part of ISO 11607 is applicable to industry, to health care facilities, and wherever medical devices are placed in sterile

French and Russian

small premises covered in Clause 10 of BS 5588-11

Management review

Annex E is a non-mandatory procedure for establishing the flow resistance of a burst bursting disc assembly

This code of practice does not deal with the protection afforded to a floor by floor coverings or surface finishes

prison access/egress

This part of BS 8000 provides a context for the activities described in the individual parts

Over the past decade

Inclusion of a new enquiry case 5500/139 for the ISO 16528-2:2007 Conformance Tables

EN 60512-25-1

Retailers and users of these panels

IEC 60270:1981