Catalog Number

-

Brand Name

Well at Walgreens

Version/Model Number

307762

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FQM

Product Code Name

Bandage, Elastic

Public Device Record Key

3e24bc23-aa8c-45b0-9e52-2ddfd46d6dab

Public Version Date

September 20, 2021

Public Version Number

2

DI Record Publish Date

May 22, 2020

Package DI Number

10049022739304

Quantity per Package

72

Contains DI Package

00049022739307

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

carton