Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

12-728-09

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

5d815b0f-5e19-4c03-80a3-6064eb2322c3

Public Version Date

August 24, 2021

Public Version Number

3

DI Record Publish Date

August 20, 2016

Package DI Number

20809160004231

Quantity per Package

10

Contains DI Package

10809160004234

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-