GB 12264-1990
Replaced
YY/T 1839-2022
Active
Industry standards-Medicine
YY/T 1839-2022 Cardiopulmonary bypass systems—Venous bubble traps
YY/T 1839-2022 Cardiopulmonary bypass systems—Venous bubble traps
Basic Information
Standard Code:
YY/T 1839-2022
Standard Type:
Industry standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
Extracorporeal circulation, artificial organs, and prosthetic devices
ICS Name:
Surgical implants, prostheses, and orthoses
Publish Date:
2022-05-18
Implement Date:
2023-06-01
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:
28 pages
Scope
本文件规定了体外循环支持的手术过程中,用于排除静脉气泡的一次性使用无菌静脉气泡捕获器的要求和试验方法。
本文件适用于一次性使用无菌静脉气泡捕获器。
注: 需要体外循环支持的手术过程可包括心肺转流、体外膜肺氧合、活体移植静脉转流等。
Development Information
Drafting Units:
广东省医疗器械质量监督检验所、迈柯唯(上海)医疗设备有限公司、天津市塑料研究所有限公司
Drafting Persons:
徐苏华、梁泽鑫、李生霞、洪良通、聂永胜、陈华燕、柯军、何晓帆、颜林
Referenced Standards
YY/T 1556-2017 Test methods for particle contamination of infusion,transfusion and injection equipments for medical use
ISO 80369-7:2016
中华人民共和国药典
GB/T 14233.1-1998 Infusion,transfusion,injection equipment for medical use—Part 1:Chemical analysis methods
GB/T 14233.1-2008 Test methods for infusion,transfusion,injection equipments for medical use—Part 1:Chemical analysis methods
GB/T 14233.1-2022 Test methods for infusion,transfusion,injection equipments for medical use—Part 1:Chemical analysis methods
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 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
YY/T 0681.1-2009 Test methods for sterile medical device package—Part 1:Test guide for accelerated aging
YY/T 0681.1-2018 Test methods for sterile medical device package—Part 1:Test guide for accelerated aging
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 18241:2016
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