Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

77453

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 22, 2022

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

f3944e81-5499-4631-b75f-655b4fd365c0

Public Version Date

July 25, 2022

Public Version Number

6

DI Record Publish Date

October 18, 2017

Package DI Number

20809160167073

Quantity per Package

16

Contains DI Package

10809160167076

Package Discontinue Date

July 22, 2022

Package Status

Not in Commercial Distribution

Package Type

-