Catalog Number

-

Brand Name

Medical Action Industries

Version/Model Number

69003

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

GAX

Product Code Name

TOURNIQUET, NONPNEUMATIC

Public Device Record Key

22bc11fe-de0a-480a-a808-b34c135c9fee

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

August 20, 2016

Package DI Number

20809160013073

Quantity per Package

100

Contains DI Package

10809160013076

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-