Catalog Number

3130LF

Brand Name

T.E.D.

Version/Model Number

3130LF

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

July 01, 2023

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

0d5618a0-f6ff-4bb3-88f0-7b2a1f729e04

Public Version Date

November 26, 2020

Public Version Number

8

DI Record Publish Date

September 24, 2016

Package DI Number

20884521001630

Quantity per Package

36

Contains DI Package

00884521001636

Package Discontinue Date

July 01, 2023

Package Status

In Commercial Distribution

Package Type

CASE