1Key Takeaways
This European Standard specifies test methods and values for sealable adhesive coated paper manufactured from paper complying with EN 868-6, used as sterile barrier systems and/or packaging systems that are intended to maintain sterility of terminally sterilized medical devices to the point of use. The materials specif…
2Scope / Description
This European Standard specifies test methods and values for sealable adhesive coated paper manufactured from paper complying with EN 868-6, used as sterile barrier systems and/or packaging systems that are intended to maintain sterility of terminally sterilized medical devices to the point of use. The materials specified in this part are intended to be used for ethylene oxide or irradiation sterilization. Other than the general requirements as specified in EN ISO 11607-1 and EN ISO 11607-2 this part of EN 868 specifies materials, test methods and values that are specific to the products covered by this European Standard. The materials specified in this part of EN 868 are intended for single use only.
5Citation Network
Standards that cite EN 868-7:2017
Referenced by EN 868-7:2017
93/42/EWG-1993
EN 1041:2008
EN 20187:1993
EN ISO 11607-1/A1:2014
EN ISO 11607-1:2009
EN ISO 11607-2:2006
EN ISO 1924-2:2008
EN ISO 1974:2012
6Frequently Asked Questions
What is EN 868-7:2017?
EN 868-7:2017 — Packaging for terminally sterilized medical devices - Part 7: Adhesive coated paper for low temperature sterilization processes - Requirements and test methods is an international standard developed by European Committee for Standardization (CEN). This European Standard specifies test methods and values for sealable adhesive coated paper manufactured from paper complying with EN 868-6, used as sterile barrier systems and/or packaging systems that are intended to maintain sterility of...
What does EN 868-7:2017 cover?
This standard covers: This European Standard specifies test methods and values for sealable adhesive coated paper manufactured from paper complying with EN 868-6, used as sterile barrier systems and/or packaging systems that are intended to maintain sterility of terminally sterilized medical devices to the point of use....
Who should use this standard?
This standard is intended for organizations, professionals, and stakeholders involved in various industries and sectors. It is applicable to manufacturers, service providers, regulatory bodies, and certification organizations.
What is the latest version of EN 868-7:2017?
The current published version is EN 868-7:2017, published on 2017-02. Always check for amendments or pending revisions.
How do I purchase EN 868-7:2017?
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