Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

8300

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

MDM

Product Code Name

INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

Public Device Record Key

e8441054-a1f5-48b8-9f4b-c538fd071d11

Public Version Date

March 22, 2022

Public Version Number

4

DI Record Publish Date

August 20, 2016

Package DI Number

20809160023836

Quantity per Package

25

Contains DI Package

10809160023839

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-