YY/T 1271-2016 Active Industry standards-Medicine

YY/T 1271-2016 Cardiopulmonary bypass systems—Suction catheter for single use

YY/T 1271-2016 Cardiopulmonary bypass systems—Suction catheter for single use

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/T 1271-2016
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: 8 pages

Scope

This standard specifies the classification and structure, requirements, test methods, marking, labeling, user manuals, packaging, transportation, and storage of sterile single-use suction tubes (hereinafter referred to as suction tubes).
This standard applies to suction tubes used in cardiopulmonary bypass systems for cardiovascular surgery, such as left heart deflation, suctioning to reduce pressure or left heart load, and suctioning of blood and other fluids within the surgical field of the heart.

Development Information

Word Count: 13 Thousand words Pages: 8 pages

Referenced Standards

GB/T 191-2008 Packaging—Pictorial marking for handling of goods GB/T 9969-2008 General principles for preparation of instructions for use of industrial products 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 YY/T 0149-2006 Medical instruments of stainless steel—Test methods of corrosion resistance 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

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