13.340.30 呼吸保护装置 标准查询与下载

GB/T 2626-1992 自吸过滤式防尘口罩通用技术

本标准规定了自吸过滤式防尘口罩（以下简称防尘口罩）的术语、分类、技术要求、试验方法、检验规则、标志、包装、运输、贮存和使用。 本标准适用于生产、销售和使用的各类防尘口罩。 本标准不适用于环境中氧低于18％和有毒气体使用的呼吸器。

General technical requirements for self-inhalation filtertype dust respirator

GB/T 8160-1987 矿用一氧化碳过滤式自救器试验方法

本标准适用于评价矿用一氧化碳过滤式自救器（以下简称自救器），是否符合产品标准的要求，并可作为该产品质量控制的试验手段。

Test methods of mine filter self rescuer for carbon monoxide

GB 8159-1987 矿用一氧化碳过滤式自救器

本标准适用于矿山井下个人脱险使用的防一氧化碳过滤式自救器（以下简称自救器）。

Mine filter self rescuer for carbon monoxide

GB/T 6224.3-1986 过滤式防微粒口罩死腔的试验方法

本方法用于测试口罩戴在标准头型上，口罩与头型面部间之死腔，以此来评价口罩是否符合卫生学要求及口罩设计方针。

Test method for the dead space of filtering particle respirator

GB/T 6224.2-1986 过滤式防微粒口罩过滤效率的试验方法

本方法适用于测定过滤式防微粒口罩在规定条件下的过滤效率，以评价口罩对有害微粒的防护能力。

Test method for filter efficiency of filtering particle respirator

GB/T 6224.1-1986 过滤式防微粒口罩总透漏率的试验方法

本方法用于测定防微粒口罩在人员佩戴时的总透漏率，以综合评价防微粒口罩对有害微粒的实际防护性能和口罩设计制造的质量。

Test method for total inward leakage of filtering particle respirator

GB/T 6224.4-1986 过滤式防微粒口罩对空气流呼吸阻力的试验方法

本方法用于测定防微粒口罩在规定条件下的吸气和呼气阻力。试验时把口罩戴在实验头型上，将稳定流速的空气流通过口罩，抽气所形成的负压值为口罩的吸气阻力，吹气所形成的正压值为呼气阻力，结果以Pa（mmH2O）表示。

Test method for airflow resistance of respiration of filtering particle respirator

GSO ISO 16900-1:2024 呼吸防护装置 试验方法和试验设备 第1部分：内泄漏量的测定

This document specifies the test methods for determining inward leakage of respiratory interfaces (RI) and total inward leakage of complete respiratory protective devices (RPD) using specified test agents and incorporating specified body movements, at specified metabolic work rates. These tests are conducted in laboratories using specific test agents under specified conditions and therefore do not indicate the performance of the device in actual use.

Respiratory protective devices — Methods of test and test equipment — Part 1: Determination of inward leakage

GSO ISO/TS 17420-8:2024 呼吸防护装置 性能要求 第8部分：特殊应用化学、生物、放射和核 (CBRN) 过滤和放射 核 (RN) 过滤 RPD

This document specifies the requirements for respiratory protective devices for use by workers during response to incidents involving chemical, biological radiological or nuclear (CBRN) materials used with intent to cause harm or in cases of accidental release outside traditional hazardous materials response categories. For the purposes of this document, all incidents described here are named CBRN incidents. This document is applicable to RPD for use by personnel in the following roles: —    First responders: including police, fire service, emergency medical, search and rescue, sampling and detection teams. —    Workers needed for specific roles during response (utility, transportation, service continuity). —    Medical personnel working with casualties of CBRN incidents. —    Responders to release incidents involving nuclear materials. —    Non-emergency but CBRN-related roles. —    Workers in need of protection during escape from a CBRN or radiological release incident. —    Workers in need of protection from nuclear materials. The requirements for RPD use by the following groups are not addressed by this document: —    Military personnel outside of first responder roles. —    Children. —    Animals. Requirements for the following are not covered by this document: —    Collective protection systems including ventilated casualty/body bags. —    Methods of and criteria for decontamination of RPD. —    Disposal of used equipment. This document is focused on respiratory protection requirements, but it is recognised that CBRN RPD are always used as part of an ensemble with protective clothing. The total ensemble effectiveness is not covered by this document.

Respiratory protective devices — Performance requirements — Part 8: Special application chemical, biological, radiological and nuclear (CBRN) filtering and radiological-nuclear (RN) filtering RPD

24/30471766 DC 呼吸防护装置 试验方法和试验设备 第11部分：视野的测定

Respiratory protective devices — Methods of test and test equipment - Part 11: Determination of field of vision

T/QGCML 2484-2023 Pss BG4正压氧气呼吸器更换氧气瓶技术指南

本文规定了Pss BG4正压氧气呼吸器更换氧气瓶技术指南的术语和定义、更换目的、自换和互换的概念、前提条件、操作程序、更换步骤和注意事项。 本文件适用于Pss BG4正压氧气呼吸器更换氧气瓶技术的操作及应用。

Pss BG4 Positive Pressure Oxygen Respirator Technical Guide for Replacing Oxygen Cylinders

T/QGCML 2483-2023 Pss BG4正压氧气呼吸器更换HY2(ZYHS120)正压氧气呼吸器技术指南

本文件规定了HY2(ZYHS120)正压氧气呼吸器的术语与定义、适用环境、技术参数、仪器结构、操作人员要求、更换流程、保养及注意事项。 本文件适用于HY2(ZYHS120)正压氧气呼吸器的技术指南的推广及应用。

Pss BG4 Positive Pressure Oxygen Respirator Replacement HY2 (ZYHS120) Positive Pressure Oxygen Respirator Technical Guide

ASTM F3387-23 呼吸防护标准实施规程

Standard Practice for Respiratory Protection

T/SXJP 060-2023 大眼窗防毒面具

3 术语和定义 GB/T 12903 界定的以及下列术语和定义适用于本文件。 3.1 大眼窗防毒面具 靠佩戴者自主呼吸克服部件阻力，防御有毒、有害气体或蒸气、颗粒物（如毒烟、毒雾） 等危害其呼气系统或眼面部的净气式大眼窗防护用品。 [来源：GB 2890-2022，3.1 有修改] 4 要求 4.1 面罩性能 4.3 其他技术要素 4.3.1 面罩视野 a）总视野：≥70% b) 双目视野≥56% c) 下方视野≥35° 4.3.2 镜片透光率 不小于89% 4.4 装配气密性 面罩在（1900-2300）Pa压力下，水下30s内不出现连续气泡。 4.5 其它

Gas mask with large eye window

23/30471849 DC BS 8647 呼吸设备 全脸呼吸管面罩 规格及测试方法

BS 8647. Respiratory equipment. Full-face snorkel masks. Specification and test method

EN 134:2023 呼吸保护装置.元部件命名

This document specifies the nomenclature for typical components of respiratory protective devices. It does not specify which or how many components are used and where they are located in the apparatus. The illustrations used are given as examples only for the identification of the different parts and the corresponding terms for facilitating the application. The terms and definitions used are given in EN ISO 16972:2020 and EN 135:1998. The terms are given in the three official CEN languages.

Respiratory protective devices - Nomenclature of components

GSO 2707:2023 非医用口罩

  Scope is not provided for this standard

The non-Medical Masks

ASTM E2952-23 空气净化呼吸防护烟雾逃生装置 (RPED) 标准规范

1.1 This specification covers the minimum requirements for the design, performance, testing, and certification of airpurifying respiratory protective smoke escape devices for immediate emergency evacuation without entry/re-entry. 1.2 The purpose of this specification shall be to provide minimum requirements for respiratory protective escape devices that provide limited protection for 15 min for escape from the by-products of fire, including particulate matter, carbon monoxide, other toxic gases, and the effects of radiant heat. 1.3 The requirements of this specification specify an airpurifying respiratory protective escape device with a laboratory-tested 15-min service life intended to provide head, eye, and respiratory protection from particulate matter, irritants, and toxic gases and vapors commonly produced by fire. 1.4 Controlled laboratory tests that are used to determine compliance with the performance requirements of this specification shall not be deemed as establishing performance levels for all situations to which individuals can be exposed. 1.5 This specification shall not apply to the requirements for provision, installation, or use of air-purifying respiratory protective smoke escape devices. 1.6 This specification shall not apply to respiratory protective escape devices intended for use in circumstances in which an oxygen deficiency (oxygen less than 19.5 % by volume) exists or might exist. 1.7 This specification is not intended to be used as a detailed manufacturing or purchase specification, but shall be permitted to be referenced as a minimum requirement in purchase specifications. 1.8 The conformity assessment requirements of Guide F3050, Model C, shall apply to the certification of products in accordance with this specification. 1.9 Units—The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.10 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use. 1.11 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.

Standard Specification for Air-Purifying Respiratory Protective Smoke Escape Devices (RPED)

BS ISO 16976-7:2023 呼吸防护装置 人为因素 听力和言语

1   Scope This document contains information related to the interaction between respiratory protective devices and the human body functions of hearing and speech.

Respiratory protective devices. Human factors - Hearing and speech

ASTM F3502-23a 屏障表面覆盖物的标准规范

1.1 This specification is intended to help ensure barrier face coverings meeting the stated requirements provide (1) a means of source control for individual wearers by reducing expelled aerosols from the wearer’s nose and mouth into the air; and (2) a degree of particulate filtration that potentially reduces the amount of aerosols inhaled by the wearer. NOTE 1—The source control/protection provided by barrier face coverings depends on several factors not considered in this specification, such as material degradation from wearer challenges including perspiration, talking, sneezing, and the length of time the barrier face covering is worn. Further research is needed to expand the evidence base for the protective effect of face coverings and, in particular, to identify the combinations of materials that maximize both their blocking and filtering effectiveness, as well as fit, comfort, durability, and consumer appeal. (https:// www.cdc.gov/coronavirus/2019-ncov/more/masking-science-sarscov2.html.) NOTE 2—There are currently no established methods for measuring outward leakage from a barrier face covering, medical mask, or respirator. 1 This specification is under the jurisdiction of ASTM Committee F23 on Personal Protective Clothing and Equipment and is the direct responsibility of Subcommittee F23.65 on Respiratory. Current edition approved April 1, 2023. Published April 2023. Originally approved in 2021. Last previous edition approved in 2023 as F3502 – 23. DOI: 10.1520/F3502-23A. Copyright © ASTM International, 100 Barr Harbor Drive, PO Box C700, West Conshohocken, PA 19428-2959. United States This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee. 1 Nothing in this specification addresses or implies a quantitative assessment of outward leakage and no claims can be made about the degree to which a barrier face covering reduces expired human-generated aerosols. 1.2 This specification establishes minimum design, performance (testing), labeling, user instruction, reporting and classification, and conformity assessment requirements for barrier face coverings. 1.2.1 Design criteria include setting minimum areas of face coverage over the wearer’s nose and mouth, prohibiting open vents or valves, requiring a means for retaining the barrier face covering on the wearer’s head, and providing a representation of product sizing. Manufacturers are further required to perform a design analysis for assessing leakage of exhaled air from the barrier face covering where the general approach is described in the product report. Manufacturers are permitted to conduct quantitative testing as specified in this specification to supplement the design analysis. Accessories, such as braces or other devices that allow the barrier face covering to better conform to the wearer’s face, are addressed as part of this specification if used for the purpose of reducing leakage. 1.2.2 Performance and testing criteria define minimum barrier face covering filtration efficiency and airflow resistance performance properties. Sub-micron particulate filtration efficiency represents the ability to capture and reduce respirable aerosols that potentially contain viruses and bacteria. Airflow resistance represents the wearer’s ease of breathing or breathability while wearing the barrier face covering. The impact of repeated cleaning or laundering on continued performance is applied for measuring performance properties for those barrier face coverings that are intended for reuse. Manufacturers are permitted to also provide test results for bacterial filtration efficiency (BFE) as supplemental information to the mandatory performance measurement of sub-micron particulate filtration efficiency. NOTE 3—The principal performance criteria for barrier face covering determined by testing are sub-micron particle filtration efficiency and airflow resistance. Quantitative leakage assessment testing is optional for information purposes and is not required. This testing is not likely to be representative of outward leakage from the barrier face covering and should not be claimed to represent the amount of source control offered by the face covering. Bacterial filtration efficiency testing is also optional and not required. It is significantly different than sub-micron filtration efficiency, and the results of BFE testing cannot be interchanged or directly compared. 1.2.3 Labeling requirements specify the minimum content for labels that appear on the barrier face covering, its immediate packaging, and if different, point-of-sale packaging. 1.2.4 User instructions are required to guide selection and sizing, proper use (positioning and adjustment), and care including cleaning or laundering if product reuse is intended; inform on product cautions and limitations; and describe product replacement and disposal procedures. 1.2.5 Conformity assessment is demonstrated with a Supplier Declaration of Conformity (SDOC) following Guide F3050, Annex A3, Model A. The SDOC states that each barrier face covering labeled as compliant has met all of the requirements of this specification including design criteria, performance criteria, test methods, labeling, and user information. Additionally, conformance to this specification requires that sub-micron particulate filtration efficiency and airflow resistance tests have been performed by a laboratory accredited for conducting these tests. NOTE 4—This specification does not provide for any form of provisional, limited, or partial conformance of barrier face coverings since their compliance with this specification is a function of meeting all performance requirements, including specific filtration efficiency and breathability requirements, as well as all applicable design, labeling, reporting, and user information requirements. 1.3 This specification addresses barrier face coverings that are either disposable or reusable. 1.4 This specification does not address the unique additional performance attributes of barrier face coverings that exist for certain applications, such as flame-resistant apparel used in environments where there are flame, high heat, electrical arc, or related hazards, but does recommend that barrier face coverings also conform to other standards as applicable. 1.5 This specification does not address the use of antimicrobial or antiviral materials, finishes, or mechanisms, nor the use of drugs, biologics, or nanoparticles in barrier face coverings. This specification also does not address the efficacy of cleaning agents or other chemicals for cleaning, disinfecting, or sanitizing barrier face coverings. NOTE 5—Claims made about the use of antimicrobial materials, finishes, or mechanisms; or the use of drugs, biologics, or nanoparticles in any product subject the manufacturer to regulatory oversight by government agencies, including the U.S. Food and Drug Administration in the United States, which applies additional safety and efficacy requirements to these products. See 5.1.2 for the requirement of nontoxic and nonirritating materials used in the construction of barrier face coverings. 1.6 This specification does not address requirements for medical face masks, which are covered in Specification F2100. 1.7 Nothing in this specification is intended to contradict or replace criteria that are established in 42 CFR Part 84 for air-purifying respirators or requirements for use of respirators in accordance with 29 CFR 1910.134. 1.8 Nothing in this specification is intended to imply that barrier face coverings qualify as approved respiratory protection devices or have FDA clearance for use in a healthcare setting. 1.9 Nothing in this specification is intended to imply that barrier face coverings should be placed on very young children (

Standard Specification for Barrier Face Coverings