Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

44212

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

NAB

Product Code Name

Gauze/sponge,nonresorbable for external use

Public Device Record Key

3878b579-0270-4055-b348-9f6f2e059049

Public Version Date

August 24, 2021

Public Version Number

3

DI Record Publish Date

August 20, 2016

Package DI Number

30809160000933

Quantity per Package

25

Contains DI Package

10809160000939

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-