Catalog Number

-

Brand Name

Well at Walgreens

Version/Model Number

265333

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

NAD

Product Code Name

Dressing, Wound, Occlusive

Public Device Record Key

6107348e-2252-4b42-94b6-5c34fd87b134

Public Version Date

June 19, 2020

Public Version Number

2

DI Record Publish Date

June 04, 2020

Package DI Number

10311917156962

Quantity per Package

24

Contains DI Package

00311917156965

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case Pack