Catalog Number

-

Brand Name

3PLY SURGICAL MASK

Version/Model Number

FM-EU2001

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

QKR

Product Code Name

Face Mask Per Enforcement Policy For Face Masks And Respirators During The Declared Public Health Emergency

Public Device Record Key

496c1fdf-ee96-4f77-96a7-e84646028638

Public Version Date

March 28, 2022

Public Version Number

1

DI Record Publish Date

March 18, 2022

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-