National Personal Protective Technology Laboratory (NPPTL)
Updated December 9, 2020
For more information on COVID-19 and PPE, please visit:
Respirator Information
Respiratory Resources for Healthcare Professionals
- Reusable Elastomeric Respirators in Health Care: Considerations for Routine and Surge Useexternal icon
- Healthcare Respiratory Protection Resources Web Page
- Healthcare Workers’ Respiratory Protection Trainingexternal icon
- NIOSH Research Highlights Importance of Rigorous Standards for Gowns Used to Protect Healthcare Workers
- Preparedness through Daily Practice: The Myths of Respiratory Protection in Healthcare
- Respiratory Protection Education & Resources Webkitexternal icon
- Implementing Hospital Respiratory Protection Programs: Strategies from the Fieldexternal icon
- Hospital Respiratory Protection Program Toolkit
News
- Read the new technical report, Filtering Facepiece Respirators with an Exhalation Valve: Measurements of Filtration Efficiency to Evaluate Their Potential for Source Control.
- View archived recording of Elastomeric Half-Mask Respirator (EHMR) Federal Register Notice (FRN) Webinarexternal icon (November 18, 2020)
- PPE CASE 2020-0113 – Filtration Efficiency Performance of Non-NIOSH-Approved International Respiratory Protective Devices: Phase Two
- View recording of Factors to Consider when Planning to Purchase Respirators from Another Country, Including KN95 Respirators from China webinar.
- FDA Emergency Use Authorizations
FDA EAUs can be found at https://www.fda.gov/emergency-preparedness-and-response/mcm-legal-regulatory-and-policy-framework/emergency-use-authorization#2019-ncovexternal icon
- NIOSH-Approved Disposable Filtering Facepiece Respirators for Use in Health Care Settings During Response to the COVID-19 Public Health Emergency
- Imported, Non-NIOSH-Approved Disposable Filtering Facepiece Respirators
- CA-2018-1010R1.0 – Interim guidance regarding applications for NIOSH Approval of Filtering Facepiece Respirators in accordance with the Food and Drug Administration (FDA) Final Order published May 17, 2018, and FDA/NIOSH MOU 225-18-006, dated November 2017 (included as a reference in this notice). Revision Supersedes the November 2018 version
- CA-2020-1030 – Requirements and Responsibilities of Approval Holders and Assignees in NIOSH Approved Respirator Private Labeling and Private Packaging Arrangements
Personal Protective Technology
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Page last reviewed: December 9, 2020
Content source: National Institute for Occupational Safety and Health