FDA Reissues EUA for Certain Imported Disposable Filtering Facepiece Respirators (FFRs)

These revisions allow for emergency use of certain Non-NIOSH, Imported FFRs to remain authorized by remaining on Exhibit 1.

If your email program has trouble displaying this email, view as a webpage. FDA Reissues EUA for Certain Imported Disposable Filtering Facepiece Respirators Today, the U.S. Food and Drug Administration (FDA) reissued the Emergency Use Authorization (EUA) for imported, non-NIOSH-approved, disposable filtering facepiece respirators (FFRs)  manufactured in countries other than China. The FDA revised and reissued this EUA to authorize for emergency use only those respirators listed in the EUA's Exhibit 1 as of the date of this reissuance. Effective immediately, the FDA will no longer be reviewing requests and adding new respirator models to Exhibit 1 of this EUA. Read More Questions? If you have questions about Emergency Use Authorizations related to respirators, contact the Division of Industry and Consumer Education.

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