YY 0948-2015 Active Industry standards-Medicine

YY 0948-2015 Cardiopulmonary bypass systems—Arteriovenous cannula for single use

YY 0948-2015 Cardiopulmonary bypass systems—Arteriovenous cannula for single use

Publish Date: 2015-03-02 Implement Date: 2017-01-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: YY 0948-2015
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: 2015-03-02
Implement Date: 2017-01-01
Pages: 8 pages

Scope

This standard specifies the classification and structure, requirements, test methods, marking, labeling, user's manual, packaging, transportation, and storage of sterile single-use arterial-venous catheters (hereinafter referred to as arterial-venous catheters).
This standard applies to arterial-venous catheters used in conjunction with cardiopulmonary bypass systems for drainage or infusion of blood during open-heart surgery performed in extracorporeal circulation.

Development Information

Word Count: 14 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

Related Standards

Contact Us