Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

80075

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

6a0d65ce-71a6-4255-994a-37bb7c1a4503

Public Version Date

November 06, 2020

Public Version Number

3

DI Record Publish Date

August 20, 2016

Package DI Number

20809160021252

Quantity per Package

50

Contains DI Package

10809160021255

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-