Catalog Number

-

Brand Name

Well at Walgreens

Version/Model Number

995034

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

NAB

Product Code Name

Gauze / Sponge,Nonresorbable For External Use

Public Device Record Key

275cd375-1fe5-46ac-825e-2c1572cfd6cf

Public Version Date

August 24, 2021

Public Version Number

2

DI Record Publish Date

June 04, 2020

Package DI Number

10311917194445

Quantity per Package

48

Contains DI Package

00311917194448

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case