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
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
Superseded by the following standards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
GB 12264-1990
Replaced
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