Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

76771

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

KDD

Product Code Name

Kit, surgical instrument, disposable

Public Device Record Key

be35008c-872d-4932-9b63-1076457b03b6

Public Version Date

June 17, 2022

Public Version Number

5

DI Record Publish Date

January 30, 2017

Package DI Number

20809160124601

Quantity per Package

20

Contains DI Package

10809160124604

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-