YY/T 0698.3-2009 English PDFUS$214.00 ยท In stock
Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email. YY/T 0698.3-2009: Packaging materials for terminal sterilized medical devices. Part 3: Paper for use in the manufacture of paper bags (specified in YY/T 0698.4) and in the manufacture of pouches and reels (specified in YY/T 0698.5). Requirements and test methods Status: Valid
Basic dataStandard ID: YY/T 0698.3-2009 (YY/T0698.3-2009)Description (Translated English): Packaging materials for terminal sterilized medical devices. Part 3: Paper for use in the manufacture of paper bags (specified in YY/T 0698.4) and in the manufacture of pouches and reels (specified in YY/T 0698.5). Requirements and test methods Sector / Industry: Medical Device & Pharmaceutical Industry Standard (Recommended) Classification of Chinese Standard: C31 Classification of International Standard: 11.080.040 Word Count Estimation: 11,185 Date of Issue: 2009-06-16 Date of Implementation: 2010-12-01 Quoted Standard: GB/T 451.2; GB/T 454; GB/T 455; GB/T 458; GB/T 465.1; GB/T 465.2; GB/T 1540; GB/T 1545; GB/T 2678.6; GB/T 7408; GB/T 7974-2002; GB/T 12914; ISO 6588-2-2005; ISO 9197; ISO 11607-1 Adopted Standard: prEN 868-3-2007, IDT Regulation (derived from): Industry standard filing Notice 2009 No. 9 Issuing agency(ies): State Food and Drug Administration Summary: This standard specifies the paper bag (YY/T 0698. 4 required), the combination of bags and coil (YY/T 0698. 5 required) paper production requirements and test methods. This part is not general requirements for ISO 11607-1 requirements increase, so that 4. 2 requirements for ISO 11607-1 can be used to demonstrate compliance with one or more of the requirements, but not all of its requirements. Paper under this Part applies to doctors for terminally sterilized medical devices packaging. YY/T 0698.3-2009: Packaging materials for terminal sterilized medical devices. Part 3: Paper for use in the manufacture of paper bags (specified in YY/T 0698.4) and in the manufacture of pouches and reels (specified in YY/T 0698.5). Requirements and test methods---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order. Packaging materials for terminal sterilized medical devices.Part 3. Paper for use in the manufacture of paper bags (specified in YY/T 0698.4) and in the manufacture of pouches and reels (specified in YY/T 0698.5) .Requirements and test methods ICS 11.080.040 C31 People's Republic of China pharmaceutical industry standards Terminally sterilized medical devices packaging materials Part 3. paper (specified YY/T 0698.4), A combination of bags and coils (YY/T 0698.5 specified) Paper production requirements and test methods Posted 2009-06-16 2010-12-01 implementation State Food and Drug Administration issued ForewordYY/T 0698 "terminally sterilized medical device packaging materials," consists of the following components. --- Part 2. Sterilization wrap material requirements and test methods; --- Part 3. paper (YY/T 0698.4 forth), a combination of bags and coils (YY/T 0698.5 forth) to produce paper Sum Test methods; --- Part 4. Paper bags - Requirements and test methods; --- Part 5. sealable bags and coil combination requirements and test methods breathable material and plastic film composition; --- Part 6. Requirements and test methods for the production of paper sterile barrier system or low temperature sterilization processes for radiation sterilization; --- Part 7. ethylene oxide or radiation sterilization production sealable adhesive paper requirements and test methods for sterile barrier system; --- Part 8. steam sterilizers repeatability requirements and test methods for sterilizing containers; --- Part 9. combination sealable bags, and the cover sheet material production without nonwovens requirements and test methods for coating polyolefin; --- Part 10. combination sealable bags, and the cover sheet material production nonwovens requirements and test methods for coating polyolefin. This section YY/T Section 30698 of. Requirements and test methods other terminally sterilized medical devices packaging material will be covered in other sections. YY/T 0698 is identical with this part prEN868-3.2007 "terminally sterilized medical device packaging material. Part 3. Bag And coil (EN868-5 specified) produced paper General requirements and test methods "(EN868-4 forth). This section of the Appendices A and B are normative appendix. This part of the National Standardization Technical Committee appliances medical infusion made. This part of the jurisdiction of the State Food and Drug Administration Jinan Medical Device Quality Supervision and Inspection Center. This part mainly drafted by. Shandong Province Medical Devices Product Quality Inspection Center, Shanghai Kindly Enterprise Development Group Company Limited. Participated in the drafting of this section. Shanghai Jianzhong medical equipment Packing Co., Ltd. The main drafters of this section. Yan Ning, Songlong Fu, Zhang Honghui, Wu Ping.IntroductionISO 116071) standard the general title "Packaging for terminally sterilized medical devices", consists of two parts. Part 1 of this standard specifies Expected before use to keep terminally sterilized medical devices to common sterile preformed sterile barrier systems, sterile barrier systems and packaging systems Sum test methods. Part 2 of this standard specifies validation requirements forming, sealing and assembly processes. Each sterile barrier system must meet the requirements of ISO 11607-1. YY/T 0698 standard can be used to demonstrate compliance with one or more of the requirements specified in ISO 11607-1. 1) EN868-1.1997 has been ISO 11607-1.2006 is replaced. Our correspondence with the ISO 11607 standard is GB/T 19633-2005 (ISO 11607.2003, IDT). Please note that the revision of GB/T 19633 of. Terminally sterilized medical devices packaging materials Part 3. paper (specified YY/T 0698.4), A combination of bags and coils (YY/T 0698.5 specified) Paper production requirements and test methods1 ScopeYY/T 0698 This section provides a paper bag (YY/T 0698.4 forth), a combination of bags and coils (YY/T 0698.5 prescribed) Requirements and test methods for the production of paper. This part is not general requirements for ISO 11607-1 requirements increase, so that 4.2 can be used to demonstrate compliance with requirements for One or more of the requirements of ISO 11607-1, but not all of its requirements. This Part of the paper is suitable for terminally sterilized medical devices Medical packaging. Note. For sterilization methods specified by the manufacturer.2 Normative referencesThe following documents contain provisions which, through reference YY/T 0698 and become part of the provisions of this section. For dated references, All subsequent amendments (not including errata content) or revisions do not apply to this section, however, encourage the agreement on this section Whether the parties can study the latest versions of these documents. For undated reference documents, the latest versions apply to this section. GB/T 451.2 Paper and paperboard quantitative determination (GB/T 451.2-2002, eqv ISO 536.1995) GB/T 454 Determination of bursting strength of paper (GB/T 454-2002, idt ISO 2758.2001) GB/T 455 Paper and board - Determination of tearing resistance (GB/T 455-2002, eqv ISO 1974.1990) GB/T 458 Paper and board - Determination of air permeability (GB/T 458-2008, ISO 5636-3.1992, MOD) GB/T 465.1 Paper and paperboard bursting strength after immersion in water assay (GB/T 465.1-2008, ISO 3689. 1983, IDT) GB/T 465.2 after soaking paper and board Determination of tensile strength (GB/T 465.2-2008, ISO 3781. 1983, IDT) GB/T 1540 Determination of absorbent paper and cardboard Cobb method (GB/T 1540-2002, neq ISO 535.1991) GB/T 1545 paper, paperboard and pulp extracts water acidity and alkalinity assay (GB/T 1545-2008, ISO 6588. 1981, MOD) GB/T 2678.6 paper, board and pulp - Determination of water soluble sulphates (conductometric titration) (GB/T 2678.6-1996, eqv ISO 9198. 1989) GB/T 7408 Data elements and interchange formats - Information interchange the date and time notation (GB/T 7408-2005, ISO 8601. 2000, IDT) GB/T 7974-2002 paper, paperboard and pulp brightness (whiteness) measured diffusion/vertical method (neq ISO 2470.1999) GB/T 12914 Paper and board - Determination of tensile strength (GB/T 12914-2008, ISO 1924-2.1994, MOD) ISO 6588-2.2005 Paper, board and pulp - Determination of pH of aqueous extracts - Part 2. Hot Extraction ISO 9197 Determination of paper, paperboard and pulp water-soluble chlorides Requested materials, sterile barrier systems and packaging systems. ISO 11607-1 Packaging for terminally sterilized medical devices - Part 13 Terms and DefinitionsTerms and definitions apply to the establishment of ISO 11607-1 YY/T 0698 to the present section. ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of YY/T 0698.3-2009_English be delivered?Answer: Upon your order, we will start to translate YY/T 0698.3-2009_English as soon as possible, and keep you informed of the progress. The lead time is typically 1 ~ 3 working days. The lengthier the document the longer the lead time.Question 2: Can I share the purchased PDF of YY/T 0698.3-2009_English with my colleagues?Answer: Yes. 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