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01 · ABSTRACT

Abstract

Sterile barrier systems play a fundamental role in ensuring patient safety by maintaining the sterility of medical devices from sterilization through point-of-use. International standards such as EN ISO 11607 emphasize the importance of package integrity, microbial barrier performance, and compatibility with sterilization processes. However, healthcare providers continue to face escalating costs associated with sterile packaging materials and sterilization operations. Traditional sterilization pouches often utilize large areas of expensive breathable material to facilitate sterilant penetration. While effective, this design can significantly increase packaging costs, particularly for high-volume users such as hospitals, central sterile supply departments (CSSDs), and medical device manufacturers.
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02 · OJS METADATA

Keywords

SterilizatiomautoclavesteamEthylene oxideSterilization Barrier systemCost reduction packagingISO 13485Medical Grade PaperDupont TyvekPlasma sterilizationGamma Sterilization
03 · PUBLICATION RECORD

Article details

JournalMedical Research Archives
IssueVol 14 No 8 (2026): Vol 14 Issue 8 August 2026
SectionArticles
Published31 August 2026
DOI10.18103/mra.2026.0475
ISSN2375-1924
04 · RIGHTS & REUSE

Rights & reuse

This article is published under a Creative Commons Attribution License (CC BY 3.0) and may be shared or distributed by anyone as long as attribution is given to the journal.

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