Catalog Number

7115

Brand Name

T.E.D.

Version/Model Number

7115

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"

-

For Single-Use

-

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

DWL

Product Code Name

Stocking, medical support (to prevent pooling of blood in legs)

Public Device Record Key

ace2a7a2-33b6-450e-aebf-af00367b4159

Public Version Date

July 07, 2020

Public Version Number

7

DI Record Publish Date

May 26, 2017

Package DI Number

30884521025091

Quantity per Package

72

Contains DI Package

10884521025097

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE