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

Publish Date: 2024-07-08 Implement Date: 2027-07-20 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

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

Word Count: 26 Thousand words Pages: 16 pages

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

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