GB 12259-1990
Abolished
YY/T 0903-2013
Active
Industry standards-Medicine
YY/T 0903-2013 Electroencephalographic biofeedback equipment
YY/T 0903-2013 Electroencephalographic biofeedback equipment
Basic Information
Standard Code:
YY/T 0903-2013
Standard Type:
Industry standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
Physiotherapy and traditional Chinese medicine instruments and equipment
ICS Name:
Treatment equipment
Publish Date:
2013-10-21
Implement Date:
2014-10-01
Pages:
11 pages
Scope
This standard specifies the definition, classification, and components of electroencephalographic biofeedback devices, as well as their requirements, test methods, inspection rules, marking, packaging, transportation, and storage.
This standard applies to electroencephalographic biofeedback devices (hereinafter referred to as "brain feedback devices").
Development Information
Referenced Standards
GB 9706.1-2007 Medical electrical equipment—Part 1:General requirements for safety
GB/T 16886.5-2003 Biological evaluation of medical devices—Part 5:Test for in vitro cytotoxicity
GB/T 16886.10-2005 Biological evaluation of medical devices—Part 10:Tests for irritation and delayed-type hypersensitivity
JJG 954-2000 Digital Electroencephalogram Mapping & Brain Electric Activity Mapping
GB/T 191-2000 Packaging—Pictorial marking for handling of goods
GB/T 191-2008 Packaging—Pictorial marking for handling of goods
GB 9706.15-1999 Medical electrical equipment—Part 1:General requirements for safety 1.Collateral standard:Safety requirements for medical electrical systems
GB 9706.15-2008 Medical electrical equipment—Part1:General requirements for safety—1.Collateral standard:Safety requirements for medical electrical systems
GB/T 14710-1993 The environmental requirements and test methods for medical electrical equipment
GB/T 14710-2009 Environmental requirement and test methods for medical electrical equipment
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
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 0466.1-2016 Medical devices—Symbols to be used with medical device labels,labelling and information to be supplied—Part 1:General requirements
YY/T 0466.1-2023 Medical devices—Symbols to be used with information to be supplied by the manufacturer—Part 1:General requirements
YY 0505-2005 Medical electrical equipment—Part 1-2:General requirements for safety—Collateral standard:Electromagnetic compatibility—Requirements and tests
YY 0505-2012 Medical electrical equipment—Part 1-2:General requirements for safety—Collateral standard:Electromagnetic compatibility—Requirements and tests
YY/T 0708-2009 Medical electrical equipment—Part 1-4:General requirements for safety—collateral standard:programmable electrical medical systems
GB/T 191-2025 Graphical symbols marking for handling and storage of packages
Related Standards
GB 12261-1990
Abolished
GB 12261-1990 Artificial heart-lung machine—Bubble oxygenator
GB 12262-1990
Abolished
GB 12262-1990 Artificial heart-lung machine—Heat exchanger
GB 2024-1994
Replaced
GB 2024-1994 Acupuncture needles
GB 10035-1994
Replaced
GB 10035-1994 The air-bag type sequential external counter-pulsation device
GB 16174.1-1996
Replaced