Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

79782

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KDD

Product Code Name

Kit, surgical instrument, disposable

Public Device Record Key

06c65487-c096-4862-b446-bbe53356b725

Public Version Date

June 17, 2022

Public Version Number

3

DI Record Publish Date

May 04, 2020

Package DI Number

20809160283247

Quantity per Package

10

Contains DI Package

10809160283240

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-