YY 0487-2004 Replaced Industry standards-Medicine

YY 0487-2004 Sterrile,single-use hydrocephalus shunts and components

YY 0487-2004 Sterrile,single-use hydrocephalus shunts and components

Publish Date: 2004-07-16 Implement Date: 2005-08-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: YY 0487-2004
Standard Type: Industry standards
Standard Status: Replaced
is_force_gb: no
CCS Name: Medical hygiene products
ICS Name: Surgical implants, prostheses, and orthoses
Publish Date: 2004-07-16
Implement Date: 2005-08-01
Pages: 16 pages

Scope

This standard specifies the requirements for single-use sterile hydrocephalus shunts and their components. This standard applies to, but is not limited to: a) Completed single-use sterile hydrocephalus shunts; b) Completed multi-use sterile hydrocephalus shunts, supplied assembled by the manufacturer, or supplied in kits for assembly by doctors; c) Components of sterile single-use shunts (individually or in combination), such as valves, valved catheters (with valved catheters), inlet catheters or outlet catheters (such as arterial catheters, peritoneal catheters, venous catheters), connectors, implantable auxiliary devices (such as anti-siphon devices, measuring devices and reservoirs, perfusion devices).

Development Information

Word Count: 28 Thousand words Pages: 16 pages

Superseded by the following standards

Referenced Standards

YY 0466-2003 Medical devices—Symbols to be used with medical device labels,labelling and information to be supplied ASTM F 640:1979 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 18278-2000 Sterilization of health care products—Requirements for validation and routine control—Industrial moist heat sterilization GB 18278.1-2015 Sterilization of health care products—Moist heat—Part 1:Requirements for the development, validation and routine control of a sterilization process for medical devices 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 7197:199

Related Standards

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