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

77f8abb2-ce32-4f3f-9e10-c06a1ebe42b7

Public Version Date

July 07, 2020

Public Version Number

7

DI Record Publish Date

September 24, 2016

Package DI Number

20884521015675

Quantity per Package

72

Contains DI Package

00884521015671

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE