SSH EN ISO 11607-1:2017

Ambalazhimi për pajisje mjekësore të sterilizuara në fazën përfundimtare - Pjesa 1: Kërkesat për materialet, sistemet e barrierave sterile dhe sistemet e ambalazhimit (ISO 11607-1: 2006, përfshirë Amd 1: 2014)

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006, including Amd 1:2014)

Scope

ISO 11607-1:2006 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.
ISO 11607-1:2006 is applicable to industry, to health care facilities, and wherever medical devices are placed in sterile barrier systems and sterilized.
ISO 11607-1:2006 does not cover all requirements for sterile barrier systems and packaging systems for medical devices that are manufactured aseptically. Additional requirements might also be necessary for drug/device combinations.
ISO 11607-1:2006 does not describe a quality assurance system for control of all stages of manufacture.

Related directives

Directives related to this standards.