Catalog Number

DOKHC2030SM

Brand Name

THERAFIRM SINGLES®

Version/Model Number

T500E0230

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

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

DWL

Product Code Name

Stocking, Medical Support (To Prevent Pooling Of Blood In Legs)

Public Device Record Key

1671b06a-194e-4c24-b1ff-944160461f86

Public Version Date

July 07, 2020

Public Version Number

3

DI Record Publish Date

December 31, 2018

Package DI Number

00721734150075

Quantity per Package

12

Contains DI Package

00721734050078

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX