YY 0604-2016 Active Industry standards-Medicine

YY 0604-2016 Cardiopulmonary bypass systems—Blood-gas exchangers(oxygenators)

YY 0604-2016 Cardiopulmonary bypass systems—Blood-gas exchangers(oxygenators)

Publish Date: 2016-03-23 Implement Date: 2018-01-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: YY 0604-2016
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: 2016-03-23
Implement Date: 2018-01-01
Pages: 16 pages

Scope

This standard specifies the requirements for blood gas exchangers (oxygenators) used in sterile, single-use cardiopulmonary bypass systems (hereinafter referred to as oxygenators). These devices are used to supply oxygen to human blood and remove carbon dioxide from the blood (extracorporeal circulation devices that assist or replace the respiratory function of the lungs).
This standard also applies to heat exchangers that are an integral part of oxygenators.
This standard does not apply to:
——implantable oxygenators;
——liquid oxygenators;
——extracorporeal circulation pipes;
——separate heat exchangers;
——separate accessories.

Development Information

Word Count: 26 Thousand words Pages: 16 pages

Replace the following standards

Referenced Standards

GB/T 14233.1-2008 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 GB 19335-2003 Blood flow products for single use—General specification GB/T 19633-2005 Packaging for terminally sterilized medical devices YY/T 0466.1-2009 Medical devices—Symbols to be used with medical device labels, labelling and information to be supplied—Part 1:General requirements YY/T 0681.1-2009 Test methods for sterile medical device package—Part 1:Test guide for accelerated aging 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 18279-2000 Medical devices—Validation and routine control of ethylene oxide sterilization GB 18279-2023 Sterilization of health-care products—Ethylene oxide—Requirements for the development,validation and routine control of a sterilization process for medical devices 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/T 18279.2-2015 Sterilization of health care products—Part 2:Guidance on the application of GB 18279.1 GB 18280-2000 Sterilization of health care products—Requirement for validation and routine control—Radiation sterilization 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 18280.2-2015 Sterilization of health care products—Radiation—Part 2:Establishing the sterilization dose GB/T 18280.3-2015 Sterilization of health care products—Radiation—Part 3:Guidance on dosimetric aspects GB/T 18280.2-2025 Sterilization of health care products—Radiation—Part 2:Establishing the sterilization dose 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 GB/T 18280.3-2025 Sterilization of health care products—Radiation—Part 3:Guidance on dosimetric aspects of development,validation and routine control

Adopt standards

ISO 7199:2009

Related Standards

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