{"product_id":"yyt0698-5-2023","title":"YY\/T 0698.5-2023 English PDF (YY\/T0698.5-2023)","description":"\u003ch1\u003eYY\/T 0698.5-2023: Packaging materials for terminal sterilized medical devices - Part 5: Sealable pouches and reels of porous materials and plastic film construction - Requirements and test methods\u003c\/h1\u003e\u003cb style=\"font-size:16px;\"\u003eDelivery:\u003c\/b\u003e 9 seconds. Download (and Email) true-PDF + Invoice.\u003cbr\u003e\u003cb style=\"font-size:16px;\"\u003eGet Quotation:\u003c\/b\u003e Click \u003ca style=\"color: blue;\" href=\"https:\/\/www.chinesestandard.net\/Cart\/Cart.aspx?YY\/T%200698.5-2023_English\" rel=\"nofollow\"\u003eYY\/T 0698.5-2023\u003c\/a\u003e (Self-service in 1-minute)\u003cbr\u003e\u003cb style=\"font-size:16px;\"\u003eNewer \/ historical versions: \u003c\/b\u003e \u003ca style=\"color: blue;\" href=\"https:\/\/www.chinesestandard.net\/PDF.aspx\/YYT0698.5-2023\"\u003eYY\/T 0698.5-2023\u003c\/a\u003e\u003ch2\u003ePreview True-PDF\u003c\/h2\u003e\u003ciframe src=\"https:\/\/www.chinesestandard.net\/Preview_PDF.aspx\/YYT0698.5-2023\" width=\"445\" height=\"600\" title=\"YY\/T 0698.5-2023 True-PDF\"\u003e\u003c\/iframe\u003e \u003cbr\u003e\u003ch2\u003eScope\u003c\/h2\u003eThis document specifies requirements and test methods for sealable pouches and reels \u003cbr\u003eof porous materials compliant with YY\/T 0698.2, 0698.3, 0698.6, 0698.7, 0698.9, or \u003cbr\u003e0698.10, and plastic film construction with Clause 4 of this document. These sealable \u003cbr\u003epouches and reels are intended to be used as sterile barrier systems and\/or packaging \u003cbr\u003esystems to maintain the sterility of finally sterilized medical devices until the point of \u003cbr\u003euse. \u003cbr\u003eIn addition to the general requirements specified in GB\/T 19633.1 and GB\/T 19633.2, \u003cbr\u003ethis document specifies the specific requirements and test methods for the materials \u003cbr\u003ecovered by this Part. \u003cbr\u003eThis document applies solely to packaging materials for single-use, terminally sterilized \u003cbr\u003emedical devices. \u003cbr\u003e\u003cbr\u003e\u003ch2\u003eBasic Data\u003c\/h2\u003e\u003ctable id=\"TableTabAbout0\" rules=\"all\" border=\"1\" style=\"font-family:Arial;font-size:Small;\"\u003e  \u003ctr id=\"TableTabRow10\"\u003e     \u003ctd id=\"TableTabCell110\" align=\"center\" font=\"bold\"\u003e \u003cb\u003eStandard ID\u003c\/b\u003e \u003c\/td\u003e    \u003ctd id=\"TableTabCell120\" align=\"center\"\u003e YY\/T 0698.5-2023 (YY\/T0698.5-2023)\u003c\/td\u003e  \u003c\/tr\u003e\n\u003ctr id=\"TableTabRow20\"\u003e     \u003ctd id=\"TableTabCell210\" align=\"center\" font=\"bold\"\u003e \u003cb\u003eDescription (Translated English)\u003c\/b\u003e \u003c\/td\u003e    \u003ctd id=\"TableTabCell220\" align=\"center\"\u003e Packaging materials for terminal sterilized medical devices - Part 5: Sealable pouches and reels of porous materials and plastic film construction - Requirements and test methods\u003c\/td\u003e  \u003c\/tr\u003e\n\u003ctr id=\"TableTabRow30\"\u003e     \u003ctd id=\"TableTabCell310\" align=\"center\" font=\"bold\"\u003e \u003cb\u003eSector \/ Industry\u003c\/b\u003e \u003c\/td\u003e    \u003ctd id=\"TableTabCell320\" align=\"center\"\u003e Medical Device and Pharmaceutical Industry Standard (Recommended)\u003c\/td\u003e  \u003c\/tr\u003e\n\u003ctr id=\"TableTabRow40\"\u003e     \u003ctd id=\"TableTabCell410\" align=\"center\" font=\"bold\"\u003e \u003cb\u003eClassification of Chinese Standard\u003c\/b\u003e \u003c\/td\u003e    \u003ctd id=\"TableTabCell420\" align=\"center\"\u003e C31\u003c\/td\u003e  \u003c\/tr\u003e\n\u003ctr id=\"TableTabRow50\"\u003e     \u003ctd id=\"TableTabCell510\" align=\"center\" font=\"bold\"\u003e \u003cb\u003eClassification of International Standard\u003c\/b\u003e \u003c\/td\u003e    \u003ctd id=\"TableTabCell520\" align=\"center\"\u003e 11.080.040\u003c\/td\u003e  \u003c\/tr\u003e\n\u003ctr id=\"TableTabRow60\"\u003e     \u003ctd id=\"TableTabCell610\" align=\"center\" font=\"bold\"\u003e \u003cb\u003eWord Count Estimation\u003c\/b\u003e \u003c\/td\u003e    \u003ctd id=\"TableTabCell620\" align=\"center\"\u003e 20,222\u003c\/td\u003e  \u003c\/tr\u003e\n\u003ctr id=\"TableTabRow70\"\u003e     \u003ctd id=\"TableTabCell710\" align=\"center\" font=\"bold\"\u003e \u003cb\u003eDate of Issue\u003c\/b\u003e \u003c\/td\u003e    \u003ctd id=\"TableTabCell720\" align=\"center\"\u003e 2023-09-05\u003c\/td\u003e  \u003c\/tr\u003e\n\u003ctr id=\"TableTabRow80\"\u003e     \u003ctd id=\"TableTabCell810\" align=\"center\" font=\"bold\"\u003e \u003cb\u003eDate of Implementation\u003c\/b\u003e \u003c\/td\u003e    \u003ctd id=\"TableTabCell820\" align=\"center\"\u003e 2024-09-15\u003c\/td\u003e  \u003c\/tr\u003e\n\u003ctr id=\"TableTabRow90\"\u003e     \u003ctd id=\"TableTabCell910\" align=\"center\" font=\"bold\"\u003e \u003cb\u003eOlder Standard (superseded by this standard)\u003c\/b\u003e \u003c\/td\u003e    \u003ctd id=\"TableTabCell920\" align=\"center\"\u003e YY\/T 0698.5-2009\u003c\/td\u003e  \u003c\/tr\u003e\n\u003ctr id=\"TableTabRow100\"\u003e     \u003ctd id=\"TableTabCell1010\" align=\"center\" font=\"bold\"\u003e \u003cb\u003eIssuing agency(ies)\u003c\/b\u003e \u003c\/td\u003e    \u003ctd id=\"TableTabCell1020\" align=\"center\"\u003e State Drug Administration\u003c\/td\u003e  \u003c\/tr\u003e\n\u003ctr id=\"TableTabRow110\"\u003e     \u003ctd id=\"TableTabCell1110\" align=\"center\" font=\"bold\"\u003e \u003cb\u003eSummary\u003c\/b\u003e \u003c\/td\u003e    \u003ctd id=\"TableTabCell1120\" align=\"center\"\u003e This standard specifies the requirements and test methods for sealable combination bags and rolls composed of breathable materials that comply with YY\/T 0698.2, 0698.3, 0698.6, 0698.7, 0698.9 or 0698.10 and plastic films that comply with Clause 4 of this document. These sealable combination bags and rolls can be used as sterile barrier systems and\/or packaging systems to maintain the sterility of terminally sterilized medical devices until use. In addition to the general requirements specified in GB\/T 19633.1 and GB\/T 19633.2, this standard specifies specific requirements and test methods for the materials covered by this part. This document applies only to packaging materials for single-use terminally sterilized medical devices.\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/table\u003e\u003cbr\u003e\u003cbr\u003e","brand":"www.ChineseStandard.us -- Field Test Asia Pte. Ltd.","offers":[{"title":"Default Title","offer_id":53335609999674,"sku":null,"price":260.0,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0821\/5737\/1706\/files\/YYT0698.5-2023EN.1_2e47b3cc-e3bc-4535-9118-5cce29387dfd.jpg?v=1776524351","url":"https:\/\/www.chinesestandard.us\/products\/yyt0698-5-2023","provider":"www.ChineseStandard.us (www.ChineseStandard.net)","version":"1.0","type":"link"}