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  • National Institute for Occupational Safety and Health (NIOSH)
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    "Standard Test Procedure (STP): Determination of Remote Gauge Leak-Flow Test for Closed-Circuit, Demand and Pressure-Demand, Self-Contained Breathing Apparatus"
    Title

    "Standard Test Procedure (STP): Determination of Remote Gauge Leak-Flow Test for Closed-Circuit, Demand and Pressure-Demand, Self-Contained Breathing Apparatus"

    This test establishes the standard procedure for ensuring that the level of protection provided by the remote gauge leak flow test requirements on Closed-Circuit, Demand and Pressure-Demand, Self-Contained Breathing Apparatus (SCBA) submitted for Approval, Extension of Approval, or examined during Post-Certification Product Audits meet the certification requirements set forth in 42 CFR, Part 84, Subpart G, Section 84.63(a)(c)(d), and Subpart H, 84.82(f)(g); Volume 60, Number 110, June 8, 1995. This STP describes the Determination of Remote Gauge Leak Flow Test for Closed-Circuit, Demand and Pressure-Demand, Self-Contained Breathing Apparatus test in sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.
    Description

    This test establishes the standard procedure for ensuring that the level of protection provided by the remote gauge leak flow test requirements on Closed-Circuit, Demand and Pressure-Demand, Self-Contained Breathing Apparatus (SCBA) submitted for Approval, Extension of Approval, or examined during Post-Certification Product Audits meet the certification requirements set forth in 42 CFR, Part 84, Subpart G, Section 84.63(a)(c)(d), and Subpart H, 84.82(f)(g); Volume 60, Number 110, June 8, 1995. This STP describes the Determination of Remote Gauge Leak Flow Test for Closed-Circuit, Demand and Pressure-Demand, Self-Contained Breathing Apparatus test in sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.

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    National Institute for Occupational Safety and Health (NIOSH)
    "Standard Test Procedure (STP): Man Test Number 6 - Self-Contained Breathing Apparatus Using Liquified Gas"
    Title

    "Standard Test Procedure (STP): Man Test Number 6 - Self-Contained Breathing Apparatus Using Liquified Gas"

    This test establishes the procedures for ensuring that the level of protection provided by the Man Test Number 6 requirements on Self-Contained Breathing Apparatus (SCBA) using liquified gas submitted for Approval, Extension of Approval, or examined during Certified Product Audits, meet the minimum certification standards set forth in 42 CFR, Part 84, Subpart G, Section 84.63(a)(c)(d), and Subpart H, Sections 84.79, 84.102, and 84.103(a)(b), Volume 60, Number 110, June 8, 1995. This STP describes the Man Test Number 6 Self-Contained Breathing Apparatus Using Liquified Gas test in sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.
    Description

    This test establishes the procedures for ensuring that the level of protection provided by the Man Test Number 6 requirements on Self-Contained Breathing Apparatus (SCBA) using liquified gas submitted for Approval, Extension of Approval, or examined during Certified Product Audits, meet the minimum certification standards set forth in 42 CFR, Part 84, Subpart G, Section 84.63(a)(c)(d), and Subpart H, Sections 84.79, 84.102, and 84.103(a)(b), Volume 60, Number 110, June 8, 1995. This STP describes the Man Test Number 6 Self-Contained Breathing Apparatus Using Liquified Gas test in sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.

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  • National Institute for Occupational Safety and Health (NIOSH)
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    "Standard Test Procedure (STP): Determination of Full Facepiece, Tight-Fitting, Negative-Pressure, Air-Purifying Respirator (APR) Performance During Dynamic Testing Against the Chemical Agent Sarin (GB) Vapor"
    Title

    "Standard Test Procedure (STP): Determination of Full Facepiece, Tight-Fitting, Negative-Pressure, Air-Purifying Respirator (APR) Performance During Dynamic Testing Against the Chemical Agent Sarin (GB) Vapor"

    This test establishes the procedures for ensuring the level of respiratory protection provided under chemical, biological, radiological, and nuclear (CBRN) protection requirements for full facepiece, tight fitting, negative pressure, air-purifying respirators (APR) submitted for approval, extension of approval, or examined during certification product audits, meet the minimum certification standards set forth in Title 42 CFR, Part 84, Subpart G, Section 84.63(a)(c)(d); Federal Register Volume 60, Number 110, June 8, 1995. This STP describes the test procedure necessary to test and certify CBRN APR. This procedure is used to test CBRN APR against Sarin (GB) vapor while the respirator, as a system, is operated in a dynamic breathing mode by means of a mechanical breather pump connected to the mouth area of a given validated manikin headform. Instrumentation is integrated under this dynamic static chamber platform for the purpose of generating and controlling challenge concentrations and detecting precise agent penetration and permeation of a tested respirator system. The procedure is a separate test under the NIOSH National Personal Protective Technology Laboratory (NPPTL) heading of CET-APRS-STP-CBRN-0350 for challenge agent Sarin (GB) vapor. This procedure is designed to rigorously test the evaluated respirator as a dynamic system and generate repeatable independent pass or fail results.
    Description

    This test establishes the procedures for ensuring the level of respiratory protection provided under chemical, biological, radiological, and nuclear (CBRN) protection requirements for full facepiece, tight fitting, negative pressure, air-purifying respirators (APR) submitted for approval, extension of approval, or examined during certification product audits, meet the minimum certification standards set forth in Title 42 CFR, Part 84, Subpart G, Section 84.63(a)(c)(d); Federal Register Volume 60, Number 110, June 8, 1995. This STP describes the test procedure necessary to test and certify CBRN APR. This procedure is used to test CBRN APR against Sarin (GB) vapor while the respirator, as a system, is operated in a dynamic breathing mode by means of a mechanical breather pump connected to the mouth area of a given validated manikin headform. Instrumentation is integrated under this dynamic static chamber platform for the purpose of generating and controlling challenge concentrations and detecting precise agent penetration and permeation of a tested respirator system. The procedure is a separate test under the NIOSH National Personal Protective Technology Laboratory (NPPTL) heading of CET-APRS-STP-CBRN-0350 for challenge agent Sarin (GB) vapor. This procedure is designed to rigorously test the evaluated respirator as a dynamic system and generate repeatable independent pass or fail results.

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    "Standard Test Procedure (STP): Determination of Full-Facepiece, Tight-Fitting, Negative-Pressure, Air-Purifying Respirator (APR) Performance During Dynamic Testing Against Chemical Agent Distilled Sulfur Mustard (HD) Vapor And Liquid"
    Title

    "Standard Test Procedure (STP): Determination of Full-Facepiece, Tight-Fitting, Negative-Pressure, Air-Purifying Respirator (APR) Performance During Dynamic Testing Against Chemical Agent Distilled Sulfur Mustard (HD) Vapor And Liquid"

    This document establishes the procedures for ensuring the level of respiratory protection provided by chemical, biological, radiological, and nuclear (CBRN) protection requirements for full facepiece, tight fitting, negative pressure, P100, CBRN Capacity X, air-purifying respirator (APR) submitted for approval, extension of approval, or examined during certification product audits, meet the minimum certification standards set forth in Title 42 CFR, Part 84, Subpart G, Section 84.63(a)(c)(d) and Federal Register, Volume 60, Number 110, June 8, 1995. This STP describes a test titled “Determination Of Full Facepiece, Tight Fitting, Negative Pressure, Air-Purifying Respirator (APR) Performance During Dynamic Testing Against Chemical Agent Distilled Sulfur Mustard (HD) Vapor And Distilled Sulfur Mustard (HD) Liquid” in sufficient detail that a team of persons knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test and determine whether or not the product passes the test. The purpose of this standard test procedure (STP) is to describe the test conditions and procedures necessary to test and certify CBRN APR certification applications. A CBRN APR is a complete tight fitting and full face blank, properly outfitted with manufacturer unique components and a properly designed manufacturer specified APR canister that is installed per the manufacturer’s installation requirements outlined in current user instructions. This procedure is used to test CBRN APR systems against distilled sulfur mustard (HD) vapor and liquid physical states, while the respirator is operated in dynamic mode by means of a breather pump connected to the breathing zone of a manikin headform. Instrumentation is integrated under this static chamber platform for the purpose of generating and controlling challenge concentrations and detecting precise agent permeation and penetration of a tested respirator. This procedure is a separate test under the NIOSH NPPTL Respirator Branch, Certification, Evaluation and Testing Section (CET) heading of CET-APRS-STP-CBRN-0351 for challenge of sulfur mustard (HD) vapor and liquid. This procedure is designed to rigorously test the evaluated respirator as a dynamic breathing system and generate repeatable independent pass or fail results under laboratory conditions.
    Description

    This document establishes the procedures for ensuring the level of respiratory protection provided by chemical, biological, radiological, and nuclear (CBRN) protection requirements for full facepiece, tight fitting, negative pressure, P100, CBRN Capacity X, air-purifying respirator (APR) submitted for approval, extension of approval, or examined during certification product audits, meet the minimum certification standards set forth in Title 42 CFR, Part 84, Subpart G, Section 84.63(a)(c)(d) and Federal Register, Volume 60, Number 110, June 8, 1995. This STP describes a test titled “Determination Of Full Facepiece, Tight Fitting, Negative Pressure, Air-Purifying Respirator (APR) Performance During Dynamic Testing Against Chemical Agent Distilled Sulfur Mustard (HD) Vapor And Distilled Sulfur Mustard (HD) Liquid” in sufficient detail that a team of persons knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test and determine whether or not the product passes the test. The purpose of this standard test procedure (STP) is to describe the test conditions and procedures necessary to test and certify CBRN APR certification applications. A CBRN APR is a complete tight fitting and full face blank, properly outfitted with manufacturer unique components and a properly designed manufacturer specified APR canister that is installed per the manufacturer’s installation requirements outlined in current user instructions. This procedure is used to test CBRN APR systems against distilled sulfur mustard (HD) vapor and liquid physical states, while the respirator is operated in dynamic mode by means of a breather pump connected to the breathing zone of a manikin headform. Instrumentation is integrated under this static chamber platform for the purpose of generating and controlling challenge concentrations and detecting precise agent permeation and penetration of a tested respirator. This procedure is a separate test under the NIOSH NPPTL Respirator Branch, Certification, Evaluation and Testing Section (CET) heading of CET-APRS-STP-CBRN-0351 for challenge of sulfur mustard (HD) vapor and liquid. This procedure is designed to rigorously test the evaluated respirator as a dynamic breathing system and generate repeatable independent pass or fail results under laboratory conditions.

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    National Institute for Occupational Safety and Health (NIOSH)
    "Standard Test Procedure (STP): Determination of Particulate Filter Penetration: Powered Air-Purifying Respirators (PAPR)"
    Title

    "Standard Test Procedure (STP): Determination of Particulate Filter Penetration: Powered Air-Purifying Respirators (PAPR)"

    This test establishes the procedure for ensuring that the level of protection provided by powered air-purifying respirator filters submitted for Approval, or examined during Certified Product Audits, meet the filter penetration requirements set forth in 42 CFR, Part 84, Subpart G, Section 84.63(a)(c)(d) and Subpart KK, Section 84.1151(a)(c), except that flow requirements of Section 84.1151(a)(c) are not used. In their place, flow requirements specified in Section 84.1156(c)(2) are applied. This is done in order that PAPR filters are tested, to the extent possible, at the minimum required air flow rate of the PAPR. This STP describes the Determination of Particulate Filter Penetration Test, Powered Air-purifying Respirator Filters Test in sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.
    Description

    This test establishes the procedure for ensuring that the level of protection provided by powered air-purifying respirator filters submitted for Approval, or examined during Certified Product Audits, meet the filter penetration requirements set forth in 42 CFR, Part 84, Subpart G, Section 84.63(a)(c)(d) and Subpart KK, Section 84.1151(a)(c), except that flow requirements of Section 84.1151(a)(c) are not used. In their place, flow requirements specified in Section 84.1156(c)(2) are applied. This is done in order that PAPR filters are tested, to the extent possible, at the minimum required air flow rate of the PAPR. This STP describes the Determination of Particulate Filter Penetration Test, Powered Air-purifying Respirator Filters Test in sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.

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    "Determination of Exhalation Resistance Test, Air-Purifying Respirators Standard Test Procedure (STP)"
    Title

    "Determination of Exhalation Resistance Test, Air-Purifying Respirators Standard Test Procedure (STP)"

    This document establishes the procedure for ensuring that the performance exhibited by air purifying respirators (APRs) submitted for Approval, Extension of Approval, or examined during Certified Product Audits, meets the minimum exhalation resistance requirements set forth in 42CFR, Part 84, Subpart I, Section 84.122; Subpart K, Section 84.172; Subpart L, Section 84.203;the Statement of Standard for Chemical, Biological, Radiological and Nuclear (CBRN) Full-Facepiece Air-Purifying Respirator (APR) Revision 2 dated 4-4-2003; and the Statement of Standard for Chemical, Biological, Radiological and Nuclear (CBRN) Air-Purifying Escape Respirator (APER) dated 9-30-2003. This STP describes the Determination of Exhalation Resistance Test, Air-purifying Respirators Test in Sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.

    Description

    This document establishes the procedure for ensuring that the performance exhibited by air purifying respirators (APRs) submitted for Approval, Extension of Approval, or examined during Certified Product Audits, meets the minimum exhalation resistance requirements set forth in 42CFR, Part 84, Subpart I, Section 84.122; Subpart K, Section 84.172; Subpart L, Section 84.203;the Statement of Standard for Chemical, Biological, Radiological and Nuclear (CBRN) Full-Facepiece Air-Purifying Respirator (APR) Revision 2 dated 4-4-2003; and the Statement of Standard for Chemical, Biological, Radiological and Nuclear (CBRN) Air-Purifying Escape Respirator (APER) dated 9-30-2003. This STP describes the Determination of Exhalation Resistance Test, Air-purifying Respirators Test in Sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.

    • Status: Current
    • Standard Type(s): Test Method
    • Hazard Type(s): Inhalation
    • PPE Type(s): Respirators, General
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    National Institute for Occupational Safety and Health (NIOSH)
    "Determination of Exhalation Valve Leakage Test, Air-Purifying Respirators Standard Test Procedure (STP)"
    Title

    "Determination of Exhalation Valve Leakage Test, Air-Purifying Respirators Standard Test Procedure (STP)"

    This document establishes the testing procedure for ensuring that exhalation valves included as part of air-purifying, or air-supplied respirators submitted for Approval, Extension of Approval or examined during Certified Product Audits, meet the minimum certification standards for leakage set forth in 42 CFR Part 84, Subpart H, Section 84.92, Subpart I, Section 84.123, Subpart J, Section 84.158, Subpart K, Section 84.173, Subpart L, Section 84.204.This STP describes the Determination of Exhalation Valve Leakage Test, Air-purifying Respirators in sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.

    Description

    This document establishes the testing procedure for ensuring that exhalation valves included as part of air-purifying, or air-supplied respirators submitted for Approval, Extension of Approval or examined during Certified Product Audits, meet the minimum certification standards for leakage set forth in 42 CFR Part 84, Subpart H, Section 84.92, Subpart I, Section 84.123, Subpart J, Section 84.158, Subpart K, Section 84.173, Subpart L, Section 84.204.This STP describes the Determination of Exhalation Valve Leakage Test, Air-purifying Respirators in sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.

    • Status: Current
    • Standard Type(s): Test Method
    • Hazard Type(s): Inhalation
    • PPE Type(s): Respirators, General
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    "Determination Of Qualitative Isoamyl Acetate (IAA) Facepiece Fit Test, Air-Purifying and Air-Supplied Respirators Standard Test Procedure (STP)"
    Title

    "Determination Of Qualitative Isoamyl Acetate (IAA) Facepiece Fit Test, Air-Purifying and Air-Supplied Respirators Standard Test Procedure (STP)"

    This document establishes the procedure for ensuring that the level of protection provided by the Isoamyl Acetate facepiece fit test requirements on air-purifying respirators (APRs) submitted for Approval or Extension of Approval meet the minimum certification standards set forth in 42 CFR Part 84, Subpart G, Section 84.63(a)(c), Subpart I, Section 84.124, Subpart K, Section 84.176, and Subpart L, Section 84.205. This standard testing procedure (STP) describes the determination of qualitative isoamyl acetate (IAA) facepiece fit test APRs in sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.

    Description

    This document establishes the procedure for ensuring that the level of protection provided by the Isoamyl Acetate facepiece fit test requirements on air-purifying respirators (APRs) submitted for Approval or Extension of Approval meet the minimum certification standards set forth in 42 CFR Part 84, Subpart G, Section 84.63(a)(c), Subpart I, Section 84.124, Subpart K, Section 84.176, and Subpart L, Section 84.205. This standard testing procedure (STP) describes the determination of qualitative isoamyl acetate (IAA) facepiece fit test APRs in sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.

    • Status: Current
    • Standard Type(s): Test Method
    • Hazard Type(s): Inhalation
    • PPE Type(s): Respirators, General
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    "Determination of Inhalation Resistance Test, Air-Purifying Respirators Standard Test Procedure (STP)"
    Title

    "Determination of Inhalation Resistance Test, Air-Purifying Respirators Standard Test Procedure (STP)"

    This document establishes the procedure for ensuring that the inhalation breathing resistance of chemical cartridge respirators, particulate respirators, gas masks, and tight-fitting powered air-purifying respirators (APRs) submitted for Approval, Extension of Approval, or examined during Certified Product Audits, meets the minimum inhalation resistance requirements set forth in 42CFR, Part 84, Subpart I, Section 84.122, Subpart K, Section 84.172, Subpart L, Section 84.203the Statement of Standard for Chemical, Biological, Radiological and Nuclear (CBRN) Full-Facepiece Air-Purifying Respirator (APR) Revision 2 dated 4-4-2003, and the Statement of Standard for Chemical, Biological, Radiological and Nuclear (CBRN) Air-Purifying Escape Respirator (APER) dated 9-30-2003.This STP describes the Determination of Inhalation Resistance Test, Air-Purifying Respirators Test in sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.

    Description

    This document establishes the procedure for ensuring that the inhalation breathing resistance of chemical cartridge respirators, particulate respirators, gas masks, and tight-fitting powered air-purifying respirators (APRs) submitted for Approval, Extension of Approval, or examined during Certified Product Audits, meets the minimum inhalation resistance requirements set forth in 42CFR, Part 84, Subpart I, Section 84.122, Subpart K, Section 84.172, Subpart L, Section 84.203the Statement of Standard for Chemical, Biological, Radiological and Nuclear (CBRN) Full-Facepiece Air-Purifying Respirator (APR) Revision 2 dated 4-4-2003, and the Statement of Standard for Chemical, Biological, Radiological and Nuclear (CBRN) Air-Purifying Escape Respirator (APER) dated 9-30-2003.This STP describes the Determination of Inhalation Resistance Test, Air-Purifying Respirators Test in sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.

    • Status: Current
    • Standard Type(s): Test Method
    • Hazard Type(s): Inhalation
    • PPE Type(s): Respirators, General
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    "Standard Test Procedure (STP): Determination of Ammonia Service-Life Test, Air-Purifying Respirators with Cartridges"
    Title

    "Standard Test Procedure (STP): Determination of Ammonia Service-Life Test, Air-Purifying Respirators with Cartridges"

    This test establishes the procedure for ensuring that the level of protection provided by air-purifying respirators with cartridges submitted for Approval, Extension of Approval, or examined during Certified Product Audits, meet the minimum certification standards set forth in 42 CFR 84, Subpart L, Section 84.207. This STP describes the Determination of Ammonia Service Life Test, Air-Purifying Respirators with cartridges test in Sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.
    Description

    This test establishes the procedure for ensuring that the level of protection provided by air-purifying respirators with cartridges submitted for Approval, Extension of Approval, or examined during Certified Product Audits, meet the minimum certification standards set forth in 42 CFR 84, Subpart L, Section 84.207. This STP describes the Determination of Ammonia Service Life Test, Air-Purifying Respirators with cartridges test in Sufficient detail that a person knowledgeable in the appropriate technical field can select equipment with the necessary resolution, conduct the test, and determine whether or not the product passes the test.

    • Status: Current
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