YY/T 1685-2020 Active Industry standards-Medicine

YY/T 1685-2020 Pneumatic impulse oscillation equipment for sputum excretion

YY/T 1685-2020 Pneumatic impulse oscillation equipment for sputum excretion

Publish Date: 2020-02-21 Implement Date: 2021-01-01 For services related to genuine standard inquiry, procurement, translation, and other related services in China, please Contact Us

Basic Information

Standard Code: YY/T 1685-2020

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: 2020-02-21

Implement Date: 2021-01-01

Pages: 8 pages

Scope

This standard specifies the terms and definitions, classification and composition, requirements, and test methods for pneumatic pulse oscillation expectoration equipment (hereinafter referred to as the equipment).
This standard applies to equipment that uses pulse airflow generated by an air pulse airflow generator, which is delivered through an air supply hose into an inflatable airbag to act on the chest cavity and assist in the removal of respiratory tract secretions. For a multi-functional device (such as those with nebulizer functions), the content specified in this standard only applies to the expectoration function based on the pneumatic pulse oscillation principle of the device. Other functions, if there are corresponding national standards and/or industry standards, should also comply with the requirements of other relevant standards.
This standard does not apply to vibration percussion expectoration machines.

Development Information

Word Count: 12 Thousand words Pages: 8 pages

Referenced Standards

GB 9706.1-1995 Medical electrical equipment—Part 1:General requirements for safety GB 9706.1-2007 Medical electrical equipment—Part 1:General requirements for safety GB 9706.1-2020 Medical electrical equipment—Part 1:General requirements for basic safety and essential performance 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 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

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