Catalog Number

-

Brand Name

McKesson

Version/Model Number

84-33

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)

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

20f3e01c-21a1-474a-91a3-a07075516acc

Public Version Date

July 07, 2020

Public Version Number

4

DI Record Publish Date

December 09, 2016

Package DI Number

40612479102581

Quantity per Package

12

Contains DI Package

10612479102573

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case