YY/T 0698.8-2009 English PDFUS$294.00 ยท In stock
Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email. YY/T 0698.8-2009: Packaging materials for terminally sterilized medical devices. Part 8: Re-usable sterilization containers for team sterilizers. Requirements and test methods Status: Valid
Basic dataStandard ID: YY/T 0698.8-2009 (YY/T0698.8-2009)Description (Translated English): Packaging materials for terminally sterilized medical devices. Part 8: Re-usable sterilization containers for team sterilizers. 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: 15,192 Date of Issue: 2009-06-16 Date of Implementation: 2010-12-01 Quoted Standard: GB/T 1220; GB/T 5783-2000; GB/T 15596; ISO 11607-1-2006; EN 285-2006 Adopted Standard: EN 868-8-2007, IDT Regulation (derived from): Industry standard filing Notice 2009 No. 9 Issuing agency(ies): State Food and Drug Administration Summary: This standard specifies the requirements and test methods for the repeated use of Yanhuo fire containers. This standard does not require a general requirement for ISO 11607-1. Therefore, the specific requirements in 4.2 to 4.5 may be used to confirm compliance with one or more of the requirements of ISO 11607-1, but not all of its requirements. The containers specified in this standard are intended for use as a packaging system for medical devices in the case of fire sterilizers conforming to EN 285. And then used for the transport and storage of equipment. NOTE 1 When the container is intended for use in steam sterilizers that do not comply with EN 285, the performance of the container in the specified sterilization cycle is confirmed by the user of the mountain, and other aspects of the suitability of the container to the freestyle cycle To perform a review, such as operation. Note 2: When YY/T 0698.8-2009: Packaging materials for terminally sterilized medical devices. Part 8: Re-usable sterilization containers for team sterilizers. 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 terminally sterilized medical devices.Part 8. Re-usable sterilization containers for team sterilizers.Requirements and test methods ICS 11.080.040 C31 People's Republic of China pharmaceutical industry standards Terminally sterilized medical devices packaging materials Part 8. repetitive use steam sterilizers Sterilization container requirements and test methods Posted 2009-06-16 2010-12-01 implementation State Food and Drug Administration issued ForewordYY/T 0698 is equivalent to using this part of EN868-8.2007 "terminally sterilized medical device packaging materials - Part 8. steam sterilization Used repetitive use of the sterile container requirements and test methods. " YY/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. Requirements and test methods other terminally sterilized medical devices packaging material will be covered in other sections. This section Appendix B, Appendix C, Appendix D, Appendix E, Appendix F is a normative appendix, Appendix A, Appendix G is informative 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, Shandong Xinhua Medical Instrument Co., Ltd. The main drafters of this section. Liang Jin Fang, Wu Ping, Sang Yonggang, Wang Hongmin.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 8. repetitive use steam sterilizers Sterilization container requirements and test methods1 ScopeYY/T 0698 This section provides the repetitive use of steam sterilization container requirements and test methods. This part is not general requirements for ISO 11607-1 requirements increase. Thus, in the 4.2 to 4.5 can be used to demonstrate compliance with special requirements One or more of the requirements of ISO 11607-1, but not all of its requirements. Container specified in this section are intended as medical devices in compliance with EN2852) steam sterilizer sterilization packaging system, then For transport and storage equipment. Note 1. This does not meet the EN285 container intended for steam sterilization, the container used in the performance of a predetermined sterilization cycle confirmed by the consumer, should also Other aspects of the Adaptability of the container and the sterilization cycle shall be reviewed, such as operating temperature. Note 2. When the device needs to be multi-layered package to meet the general requirements, devices are advised to use sterile packaging materials (such as the other part of the standard set forth in the material) package.2 Normative referencesThe following documents contain provisions which, through reference in this section YY 0698 constitute provisions of this section. Cited documents dated, its All subsequent amendments (excluding corrections) or revisions do not apply to this section, however, encourage an agreement under this section Parties to study the latest versions of these documents. For undated reference documents, the latest versions apply to this section. GB/T 1220 stainless steel rods GB/T 5783-2000 full thread hex head bolts (eqv ISO 4017.1999) GB/T 15596 Determination of plastic is exposed to sunlight or artificial light or natural climate color and performance changes under glass (GB/T 15596-1995, eqv ISO 4582. 1980) ISO 11607-1.2006 final packaging sterilized medical devices - Part 1. materials, sterile barrier systems and packaging systems requirements EN285.2006 sterilizer steam sterilizer large sterilizers3 Terms and DefinitionsTerms and definitions apply YY ISO 11607-1 and EN285 established/T 0698 to the present section.4 Requirements4.1 General ISO 11607-1 apply. Note 1. ISO 11607-1 specifies additional requirements in 5.1.10 reusable containers. Note 2. The following specific requirements and test methods can be used to demonstrate compliance with ISO 11607-1 one or more of the requirements, but not all of the requirements. Note 3. forming, sealing and assembly processes to confirm the requirements, see ISO 11607-2. 4.2 Structure and Design Requirements 2) conversion of the EN285 standard for our work in progress. 4.2.1 shapes and sizes 4.2.1.1 Container ships should be parallelepipedic box. Note. You can have a planar or curved arcuate corner portion is preferably circular. ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of YY/T 0698.8-2009_English be delivered?Answer: Upon your order, we will start to translate YY/T 0698.8-2009_English as soon as possible, and keep you informed of the progress. The lead time is typically 1 ~ 3 working days. 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