YY/T 1844-2022 Active Industry standards-Medicine

YY/T 1844-2022 Anaesthetic and respiratory equipment—General requirements for airways and related equipment

YY/T 1844-2022 Anaesthetic and respiratory equipment—General requirements for airways and related equipment

Publish Date: 2022-10-17 Implement Date: 2023-10-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us
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Basic Information

Standard Code: YY/T 1844-2022
Standard Type: Industry standards
Standard Status: Active
is_force_gb: no
CCS Name: Surgical room equipment
ICS Name: Anesthesia, respiration, and resuscitation equipment
Publish Date: 2022-10-17
Implement Date: 2023-10-01
Pages: 24 pages

Scope

This document specifies the general requirements for air ducts and related equipment.
This document is applicable to those devices for which this document is referenced in specific standards.

Development Information

Word Count: 42 Thousand words Pages: 24 pages

Referenced Standards

GB 9706.1-2020 Medical electrical equipment—Part 1:General requirements for basic safety and essential performance YY/T 0615.1-2007 Requirements for medical devices to be designated "STERILE"—Part 1:Requirements for terminally sterilized medical devices YY 9706.108-2021 Medical electrical equipment—Part 1-8:General requirements for basic safety and essential performance-Collateral standard:General requirements,tests and guidance for alarm systems in medical electrical equipment and medical electrical systems ISO 7396-1 ISO 10524-1 ISO 10524-3 ISO 14155:2011/Cor.1:2011 ISO 80369-7 EN 1041 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 18279.1-2015 Sterilization of health care products—Ethylene oxide—Part 1:Requirements for development,validation and routine control of a sterilization process for medical devices GB 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 YY/T 0586-2005 Medical polymer products—Test methods of radiopacity YY/T 0586-2016 Medical polymer products-Test methods of radiopacity YY/T 0882-2013 Anaesthetic and respiratory equipment—Compatibility with oxygen YY/T 0987.1-2016 Implants for surgery—Magnetic resonance compatibility—Part 1:Safety marking YY/T 0987.2-2016 Implants for surgery—Magnetic resonance compatibility—Part 2:Magnetically induced displacement force test method YY/T 0987.5-2016 Implants for surgery—Magnetic resonance compatibility—Part 5:Magnetically induced torque test method YY 9706.102-2021 Medical electrical equipment—Part 1-2:General requirements for basic safety and essential performance—Collateral standard:Electromagnetic compatibility—Requirements and tests 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

Adopt standards

ISO 18190:2016

Related Standards

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