YY/T 0682-2008 English PDFUS$134.00 ยท In stock
Delivery: <= 3 days. True-PDF full-copy in English will be manually translated and delivered via email. YY/T 0682-2008: Implants for surgery. Minimum data sets for surgical implants Status: Valid
Basic dataStandard ID: YY/T 0682-2008 (YY/T0682-2008)Description (Translated English): Implants for surgery. Minimum data sets for surgical implants Sector / Industry: Medical Device & Pharmaceutical Industry Standard (Recommended) Classification of Chinese Standard: C35 Classification of International Standard: 11.040.40 Word Count Estimation: 7,794 Date of Issue: 2008-10-17 Date of Implementation: 2010-01-01 Quoted Standard: GB/T 19000-2000; YY/T 0287 Adopted Standard: ISO 16054-2000, IDT Regulation (derived from): SFDA [2008] No. 605 Issuing agency(ies): State Food and Drug Administration Summary: This standard specifies the order to implant registration, tracking and analysis for the purpose of removing surgical implants with a minimum data base, and its role is to facilitate the recording and international exchange of information. Group minimum data collection requirements to the implant for the purpose of tracking, so that when the device defect unexpected event occurs, the patient can track the defective device and recall. Group also meets the minimum information for the purpose to remove the analysis and research-extension data base for the purpose of cross-reference between the core data requirements. This standard applies to implantable medical devices (implants over 30d) manufacturers and distributors, as well as perform implant operations hospitals and other medical institutions. This standard specifies the specific requirements of data items, these items should be implantable medical device manufacturers and distributors, hospitals and other medical institutions at any time after implantation and when removing documented. YY/T 0682-2008: Implants for surgery. Minimum data sets for surgical implants---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.Implants for surgery.Minimum data sets for surgical implants ICS 11.040.40 C35 People's Republic of China pharmaceutical industry standards YY/T 0682-2008/ISO 16054.2000 Surgical implants Surgical implants with minimal data group (ISO 16054.2000, IDT) Posted 2008-10-17 2010-01-01 implementation State Food and Drug Administration issued ForewordThis standard is identical with ISO 16054.2000 "Surgical implants Surgical implants with minimal information group." Appendix A of this standard is an informative annex. This standard by the national surgical implants and orthopedic instruments Standardization Technical Committee (SAC/TC110) and focal points. This standard was drafted. Tianjin, the State Food and Drug Administration Medical Device Quality Supervision and Inspection Center. The main drafters of this standard. Li Libin, Sun Huili, PROCEEDINGS, Furui Zhi. YY/T 0682-2008/ISO 16054.2000 Surgical implants Surgical implants with minimal data group1 ScopeThis standard defines an implant registration, tracking and analysis for the purpose of removing the surgical implant with minimal data group, whose role is to facilitate record And recording data on international exchange. The minimum data collection requirements to the group for the purpose of tracking implant, so that when something unexpected equipment defects When members occurs, the patient can track and recall defective devices. Groups also meet the minimum information to take out for the purpose of analysis and research - Mutual core information requirements for reference purposes between extended data base. This standard applies to implantable medical devices (implants than 30d) manufacturers and distributors, as well as to perform the implantation procedure and its hospitals His medical institutions. This standard specifies the requirements for specific information on the project, these data items by manufacturers and distributors of implantable medical devices Providers, hospitals and other medical institutions to be recorded when the implant removed and after any time. This standard is intended to define to record all events inserted and removed a minimum data base, while also providing quick inquiry with a specific patient groups The implant associated data in order to track the patient, the particular patient population refers to specific patients receiving implantable device or a group of devices overall. This standard is not to collect information for the purpose of specific medical practitioners, the medical institutions or the manufacturer, but rather to track patients for the purpose. Note. Users of this standard should ensure compliance with the data storage process involving national standards or laws and regulations.2 Normative referencesThe following documents contain provisions which, through reference in this standard and become the standard terms. For dated references, subsequent Amendments (not including errata content) or revisions do not apply to this standard, however, encourage the parties to the agreement are based on research Whether the latest versions of these documents. For undated reference documents, the latest versions apply to this standard. GB/T 19000-2000 Quality Management System - Fundamentals and vocabulary (idt ISO 9000.2000) YY/T 0287 medical device quality management system for regulatory requirements (YY/T 0287-2003, ISO 13485.2003, IDT)3 Terms and DefinitionsYY/T 0287 and the following terms and definitions and GB/T 19000-20003.1 established in applicable to this standard. 3.1 The method of any surgically implanted whole or in part, or to rely on the method of implanting the medical intervention body lumen, epithelial or substituted Ocular surfaces or surfaces; and retained at least 30 days after surgery and the only reliable method of removing a medical intervention or the passive or active treatment Treatment equipment. Note. YY/T 0287 in the active implantable medical device is separated from the definition of an implantable medical device out and given a separate definition. The standard fixed Meaning different from the definition of YY/T 0287, because it will implantable medical devices and active implantable medical devices defined separately into a single definition. 3.2 Implantable medical devices Surgery is performed when the behavior of the following operations. --- All implanted in the body, or --- Used to replace an epithelial surface or the surface of the eye, or --- Portion of the implant body. Implant surgery retain at least 30d and can only rely on medical or surgical intervention to remove. YY/T 0682-2008/ISO 16054.2000 ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of YY/T 0682-2008_English be delivered?Answer: Upon your order, we will start to translate YY/T 0682-2008_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 0682-2008_English with my colleagues?Answer: Yes. The purchased PDF of YY/T 0682-2008_English will be deemed to be sold to your employer/organization who actually pays for it, including your colleagues and your employer's intranet.Question 3: Does the price include tax/VAT?Answer: Yes. Our tax invoice, downloaded/delivered in 9 seconds, includes all tax/VAT and complies with 100+ countries' tax regulations (tax exempted in 100+ countries) -- See Avoidance of Double Taxation Agreements (DTAs): List of DTAs signed between Singapore and 100+ countriesQuestion 4: Do you accept my currency other than USD?Answer: Yes. If you need your currency to be printed on the invoice, please write an email to Sales@ChineseStandard.net. In 2 working-hours, we will create a special link for you to pay in any currencies. Otherwise, follow the normal steps: Add to Cart -- Checkout -- Select your currency to pay. |
