YY/T 1745-2021 Active Industry standards-Medicine

YY/T 1745-2021 Automated feces analyzer

YY/T 1745-2021 Automated feces analyzer

Publish Date: 2021-09-06 Implement Date: 2022-09-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: YY/T 1745-2021
Standard Type: Industry standards
Standard Status: Active
is_force_gb: no
CCS Name: Medical laboratory equipment
ICS Name: Laboratory medicine
Publish Date: 2021-09-06
Implement Date: 2022-09-01
Pages: 12 pages

Scope

This standard specifies the terms and definitions, requirements, test methods, marking, labels and instructions, packaging, transportation, and storage of automatic stool analyzers.
This standard applies to automatic or manually assisted analysis of physiological indicators and morphological components of human stool samples, and to automatic stool analyzers that provide real-time images of morphological components and other relevant information.

Development Information

Word Count: 16 Thousand words Pages: 12 pages

Referenced Standards

GB/T 14710-2009 Environmental requirement and test methods for medical electrical equipment GB/T 18268.1-2010 Electrical equipment for measurement,control and laboratory use—EMC requirements—Part 1:General requirements GB/T 18268.26-2010 Electrical equipment for measurement,control and laboratory use—EMC requirements—Part 26:Particular requirements—In vitro diagnostic (IVD) medical equipment GB/T 191-2000 Packaging—Pictorial marking for handling of goods GB/T 191-2008 Packaging—Pictorial marking for handling of goods GB 4793.1-1995 Safety requirements for electrical equipment for measurement, control, and laboratory use Part 1:General requirements GB 4793.1-2007 Safety requirements for electrical equipment for measurement, control, and laboratory use—Part 1:General requirements GB 4793.9-2013 Safety requirements for electrical equipment for measurement,control and laboratory use—Part 9:Particular requirements for automatic and semi-automatic laboratory equipment for analysis and other purposes GB 4943.1-2011 Information technology equipment—Safety—Part 1:General requirements GB 4943.1-2022 Audio/video,information and communication technology equipment—Part 1:Safety requirements GB 9254-1998 Information technology equipment—Radio disturbance characteristics—Limits and methods of measurement GB/T 9254-2008 Information technology equipment—Radio disturbance characteristics—Limits and methods of measurement GB/T 9254.1-2021 Information technology equipment,multimedia equipment and receivers—Electromagnetic compatibility—Part 1:Emission requirements GB/T 9254.2-2021 Information technology equipment,multimedia equipment and receivers—Electromagnetic compatibility—Part 2:Immunity requirements GB 17625.1-2003 Electromagnetic compatibility—limits—Limits—for harmonic current emissions(equipment input current≤16A per phase GB 17625.1-2012 Electromagnetic compatibility—Limits—Limits for harmonic current emissions(equipment input current ≤16 A per phase) GB 17625.1-2022 Electromagnetic compatibility—Limits—Part 1:Limits for harmonic current emissions(equipment input current ≤16 A per phase) GB/T 29791.3-2013 In vitro diagnostic medical devices—Information supplied by the manufacturer(labelling)—Part 3:In vitro diagnostic instruments for professional use 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 0648-2008 Safety requirements for electrical equipment for measurement,control and laboratory use—Part 2-101:Particular requirements for in vitro diagnostic (IVD) medical equipment GB/T 191-2025 Graphical symbols marking for handling and storage of packages YY/T 0648-2025 Safety requirements for electrical equipment for measurement,control,and laboratory use—Part 2-101:Particular requirements for in vitro diagnostic (IVD)medical equipment

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