Catalog Number

WRX881213

Brand Name

Walgreens

Version/Model Number

881213

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

-

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

FRO

Product Code Name

Dressing, Wound, Drug

Public Device Record Key

f9e02c89-2bd8-4a53-91c2-a86e31e25d5b

Public Version Date

November 06, 2020

Public Version Number

2

DI Record Publish Date

July 14, 2020

Package DI Number

20311917205261

Quantity per Package

6

Contains DI Package

10311917205264

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case