GB 12264-1990
Replaced
YY 0603-2024
Pending
Industry standards-Medicine
YY 0603-2024 Cardiopulmonary bypass systems—Hard-shell cardiotomy/venous reservoir systems(with/without filter) and soft venous reservoir bags
YY 0603-2024 Cardiopulmonary bypass systems—Hard-shell cardiotomy/venous reservoir systems(with/without filter) and soft venous reservoir bags
Basic Information
Standard Code:
YY 0603-2024
Standard Type:
Industry standards
Standard Status:
Pending
is_force_gb:
no
CCS Name:
Extracorporeal circulation, artificial organs, and prosthetic devices
ICS Name:
Surgical implants, prostheses, and orthoses
Publish Date:
2024-07-08
Implement Date:
2027-07-20
Publisher:
国家药品监督管理局
Technical Committee:
全国医用体外循环设备标准化技术委员会(SAC/TC 158)
Pages:
16 pages
Scope
本文件规定了无菌、一次性使用的体外循环心脏手术硬壳贮血器、硬壳静脉贮血器系统(带或不带过滤器)和静脉贮血软袋(简称贮血器)的要求,描述了相应的试验方法。贮血器拟供进行心肺转流手术(CPB)时贮血使用。本文件仅适用于多功能系统的贮血器,该系统可能有整体化部件,如血气交换器(氧合器),血液过滤器,祛泡器,血泵等。
Development Information
Replace the following standards
Referenced Standards
GB/T 14233.1-2022 Test methods for infusion,transfusion,injection equipments for medical use—Part 1:Chemical analysis methods
GB/T 14233.2-2005 Test methods for infusion,transfusion,injection equipment for medical use—Part 2:Biological test methods
YY 0580-2024 Cardiovascular implants and artificial organs—Cardiopulmonary bypass systems—Arterial blood line filters
YY/T 0681.1-2018 Test methods for sterile medical device package—Part 1:Test guide for accelerated aging
《中华人民共和国药典》2020年版四部
GB/T 16886.1-2001 Biological evaluation of medical devices—Part 1:Evaluation and testing
GB/T 16886.1-2011 Biological evaluation of medical devices—Part 1:Evaluation and testing within a risk management process
GB/T 16886.1-2022 Biological evaluation of medical devices—Part 1:Evaluation and testing within a risk management process
GB/T 16886.11-1997 Biological evaluation of medical devices—Part 11:Tests for systemic toxicity
GB/T 16886.11-2011 Biological evaluation of medical devices—Part 11:Tests for systemic toxicity
GB/T 16886.11-2021 Biological evaluation of medical devices—Part 11:Tests for systemic toxicity
GB/T 16886.12-2000 Biological evaluation of medical devices—Part 12:Sample preparation and reference materials
GB/T 16886.12-2005 Biological evaluation of medical devices—Part 12:Sample preparation and reference materials
GB/T 16886.12-2017 Biological evaluation of medical devices—Part 12:Sample preparation and reference materials
GB/T 16886.12-2023 Biological evaluation of medical devices—Part 12:Sample preparation and reference materials
GB 18279.1-2015 Sterilization of health care products—Ethylene oxide—Part 1:Requirements for development,validation and routine control of a sterilization process for medical devices
GB 18280.1-2015 Sterilization of health care products—Radiation—Part 1:Requirements for development,validation and routine control of a sterilization process for medical devices
GB/T 19974-2005 Sterilization of health care products—General requirement for characterization of a sterilization agent and the development, validation and routine control of a sterilization process for medical devices
GB/T 19974-2018 Sterilization of health care products—General requirement for characterization of a sterilization agent and the development, validation and routine control of a sterilization process for medical devices
GB 18280.1-2025 Sterilization of health care products—Radiation—Part 1:Requirements for the development,validation and routine control of a sterilization process for medical devices
Adopt standards
ISO 15674:2016
Related Standards
GB 12279-1990
Replaced
GB 12279-1990 Cardiac valve prostheses general technical specification
GB 12417-1990
Replaced
GB 12417-1990 The general technological conditions of surgical metal implant
GB/T 13461-1992
Replaced
GB/T 13461-1992 Synthetic resin blow knee prostheses
GB/T 14191-1993
Replaced
GB/T 14191-1993 Terminology for prosthetics and orthotics
GB 14722-1993
Replaced