GB/T 12279.3-2025 English PDFUS$699.00 · In stock
Delivery: <= 5 days. True-PDF full-copy in English will be manually translated and delivered via email. GB/T 12279.3-2025: Cardiovascular implants - Cardiac valve prostheses - Part 3: Heart valve substitutes implanted by transcatheter techniques Status: Valid
Basic dataStandard ID: GB/T 12279.3-2025 (GB/T12279.3-2025)Description (Translated English): Cardiovascular implants - Cardiac valve prostheses - Part 3: Heart valve substitutes implanted by transcatheter techniques Sector / Industry: National Standard (Recommended) Classification of Chinese Standard: C45 Classification of International Standard: 11.040.40 Word Count Estimation: 34,332 Date of Issue: 2025-04-25 Date of Implementation: 2026-05-01 Issuing agency(ies): State Administration for Market Regulation, China National Standardization Administration GB/T 12279.3-2025: Cardiovascular implants - Cardiac valve prostheses - Part 3: Heart valve substitutes implanted by transcatheter techniques---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. ICS 11.040.40 CCSC45 National Standard of the People's Republic of China Cardiovascular implantable devices Artificial heart valves Part 3.Transcatheter implantable prosthetic heart valves (ISO 5840-3.2021,MOD) Released on 2025-04-25 2026-05-01 implementation State Administration for Market Regulation The National Standardization Administration issued Table of contentsPreface III Introduction V 1 Scope 1 2 Normative references 1 3 Terms and Definitions 1 4 Abbreviations 3 5 Basic Requirements 4 6 Device Description 4 6.1 General 4 6.2 Intended use 4 6.3 Design Input 4 6.4 Design Output 5 6.5 Design transfer (manufacturing verification/validation) 5 6.6 Risk Management 5 7 Design Verification/Validation 6 7.1 General requirements 6 7.2 In vitro evaluation 6 7.3 Preclinical in vivo evaluation 10 Appendix A (Informative) Description of Transcatheter Valve Systems 13 A.1 General 13 A.2 Description of transcatheter valves 13 A.3 Description of the conveying system 13 A.4 Chemical treatment, surface modification or coating 13 A.5 Component Description 13 A.6 Implantation process 13 Appendix B (Informative) Transcatheter Valve Hazard Analysis Example 14 Appendix C (Informative) Fluid Dynamics Performance Verification Guidelines --- Pulsating Flow Test 16 C.1 General 16 C.2 Pulsating flow test 16 Appendix D (Normative) Transport System Design Evaluation Requirements 21 D.1 General 21 D.2 Interaction between implant and delivery system 21 D.3 Loading instruments into the delivery system 21 D.4 Entry and release capabilities 21 Appendix E (Informative) Specific Design Test Examples 23 E.1 Bracket creep 23 E.2 Environmental degradation 23 E.3 Static pressure, "burst" test 23 E.4 Calcification 23 E.5 Particle Generation 23 E.6 Effects of post-device expansion 23 E.7 Expansion Inhomogeneity 23 E.8 Evaluation of remediation options 23 E.9 Deliberate destruction of existing devices23 Appendix F (Informative) Preclinical in vivo evaluation 24 F.1 General 24 F.2 Evaluation deployment24 Reference 26ForewordThis document is in accordance with the provisions of GB/T 1.1-2020 "Guidelines for standardization work Part 1.Structure and drafting rules for standardization documents" Drafting. This document is part 3 of GB/T 12279 Cardiovascular Implantable Devices - Artificial Heart Valves. GB/T 12279 has been published. The following parts. --- Part 1.General requirements; --- Part 2.Surgical implantable artificial heart valves; --- Part 3.Transcatheter implantable prosthetic heart valves. This document is modified to adopt ISO 5840-3.2021 “Cardiovascular implantable devices - Prosthetic heart valves - Part 3.Transcatheter implantable human heart valves” Artificial Heart Valves. This document has the following structural adjustments compared to ISO 5840-3.2021. --- Deleted 7.4 in ISO 5840-3.2021; --- Table C.1 corresponds to Table C.2 in ISO 5840-3.2021; --- Deleted Annex G and Annex H in ISO 5840-3.2021. The technical differences between this document and ISO 5840-3.2021 and their reasons are as follows. ---Replace ISO 5840-1.2021 (see Chapter 5 to Chapter 7) with the normative reference GB/T 12279.1-2024.Two documents The consistency between them is modified to adapt to my country's technical conditions and improve operability; --- Use the normative reference YY/T 0640 to replace ISO 14630 (see 7.3.1). The consistency between the two documents is equal. The same, in order to adapt to my country's technical conditions and improve operability; --- Use the normative reference GB/T 16886.2 to replace ISO 10993-2 (see 7.3.2). The consistency between the two documents is equal. The same, in order to adapt to my country's technical conditions and improve operability; --- Use the normative reference YY/T 1474 to replace IEC 62366 (see 7.3.2). The consistency between the two documents is equal. The same, in order to adapt to my country's technical conditions and improve operability; --- Deleted 7.4 Clinical Research, Appendix G (Normative) Classification of Adverse Events in Clinical Research and Related References. Avoid inconsistencies with the Technical Guidelines for Clinical Evaluation of Medical Devices. The following editorial changes were made to this document. --- In order to coordinate with the existing standards, the statement of the standard scope has been changed; --- GB 9706.1 replaces IEC 60601-1 (see D.1) and GB/T 12279.2 replaces ISO 5840-2 (see Introduction), GB/T 42062 replaces ISO 14971 (see B.1), YY0285.1 replaces ISO 10555-1 (see D.1), YY/T 0663.1 replaces ISO 25539-1 (see 7.2.6.1, D.1), YY/T 0694 replaces ASTM F2079 (see 7.2.6.5), YY/T 1660 replaces ASTM F3067 (see 7.2.6.6); --- Deleted the informative reference ASTM F2081 (see 7.2.6.3 of ISO 5840-3.2021); --- Add "The values in Tables 1 and 2 apply to new or improved human Artificial heart valves” (see 7.2.4); --- Deleted the recommended reference valve information in Table C.1 of Appendix C and the description of the reference valve in C.2.3.2; --- Deleted Appendix H TAVI and TMVI preoperative, perioperative and postoperative multimodal imaging - Examples; --- Added "Steady-state flow test" in C.2.4.2; --- Changed the "pressure condition" in Table C.3 to "pressure difference across the closed valve"; --- Added "corresponding pressure difference across the closed valve (i.e. mean reverse pressure)" in C.2.7. Please note that some of the contents of this document may involve patents. The issuing organization of this document does not assume the responsibility for identifying patents. This document is proposed by the State Food and Drug Administration. This document is under the jurisdiction of the National Technical Committee for Standardization of Surgical Implants and Orthopedic Devices (SAC/TC110). This document was drafted by. China Food and Drug Inspection Institute, National Medical Products Administration Medical Device Technical Evaluation Center, Tianjin Municipal Medical Device Quality Supervision and Inspection Center, Beijing University of Aeronautics and Astronautics, Xi'an Jiaotong University, Shanghai MicroPort Cardiovascular Technology Co., Ltd., Hangzhou Venus MedTech Co., Ltd. The main drafters of this document are. Liu Li, Huang Yuanli, Wan Chenjie, Li Chongchong, Zhang Han, Ke Linnan, Gao Guanyue, Xu Yun, Miao Hui, Zhang Zhenghui, Fan Yubo, Feng Wentao, Zhang Yang, Yan Luying, Li Feifei, Liu Meirong, Zhang Heqiang.IntroductionThis document was developed for transcatheter implantable heart valve prostheses and focuses on the types of in vitro testing and preclinical in vivo evaluations, as well as All in vitro tests, reports of preclinical in vivo evaluations, device labeling and packaging. The purpose is to clarify the procedures required before the product is marketed and to Quickly identify and manage subsequent issues. GB/T 12279 Cardiovascular implantable devices - artificial heart valves aims to provide requirements and The test method is planned to consist of three parts. --- Part 1.General requirements. The purpose is to provide general requirements for artificial heart valves. --- Part 2.Surgical implantable artificial heart valves. The purpose is to give specific requirements for surgical implantable artificial heart valves. --- Part 3.Transcatheter implantable artificial heart valve. The purpose is to give the specific Require. This document needs to be used in conjunction with GB/T 12279.1-2024 and GB/T 12279.2-2024. Cardiovascular implantable devices Artificial heart valves Part 3.Transcatheter implantable prosthetic heart valves1 ScopeThis document specifies the operating conditions and performance requirements for transcatheter implantable artificial heart valves (hereinafter referred to as transcatheter valves). A method for verifying/validating the design and manufacture of transcatheter valves through risk management has been established. Appropriate verification/validation trials are selected through risk assessment. These tests include evaluation of the physical, chemical, biological, and mechanical properties of transcatheter valves and their materials and components, as well as the Preclinical in vivo evaluation of finished valve products. This document applies to all devices intended for transcatheter valve implantation, as well as newly developed and modified transcatheter valves. Accessories, packaging, and labeling required for implantation and proper sizing of transcatheter valves. This document includes considerations for implanting transcatheter valves into pre-existing devices (eg, valve-in-valve and valve-in-annulus).2 Normative referencesThe contents of the following documents constitute essential clauses of this document through normative references in this document. For referenced documents without a date, only the version corresponding to that date applies to this document; for referenced documents without a date, the latest version (including all amendments) applies to This document. GB/T 12279.1-2024 Cardiovascular implantable devices - Artificial heart valves - Part 1.General requirements (ISO 5840-1. 2021,MOD) GB/T 16886.2 Biological evaluation of medical devices Part 2.Animal welfare requirements (GB/T 16886.2-2011, ISO 10993- 2.2006,IDT) YY/T 0640 General requirements for passive surgical implants (YY/T 0640-2016, ISO 14630.2012, IDT) YY/T 1474 Application of Medical Device Usability Engineering to Medical Devices (YY/T 1474-2016, IEC 62366.2007, IDT)3 Terms and definitionsThe terms and definitions defined in GB/T 12279.1-2024 and the following apply to this document. 3.1 acute assessment Intraoperative and immediate postoperative outcomes were evaluated for in vivo safety and efficacy. NOTE. All animals participating in acute short-term assessments were kept under general anesthesia during the study. 3.2 Chronic assessment To evaluate the chronic in vivo safety and efficacy of the drug after recovery from anesthesia in animals. NOTE. The endpoints and duration of the study were determined through risk analysis. 3.3 delivery approach The anatomical pathway used to deliver the implant to the implantation site. ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of GB/T 12279.3-2025_English be delivered?Answer: Upon your order, we will start to translate GB/T 12279.3-2025_English as soon as possible, and keep you informed of the progress. The lead time is typically 3 ~ 5 working days. The lengthier the document the longer the lead time.Question 2: Can I share the purchased PDF of GB/T 12279.3-2025_English with my colleagues?Answer: Yes. 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