Catalog Number

-

Brand Name

Walgreens

Version/Model Number

NS#3120

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

K052162,K052162

Product Code

NUC

Product Code Name

Lubricant, Personal

Public Device Record Key

a9ff16d5-76bf-40e1-bb80-5e820c3a08a9

Public Version Date

August 07, 2020

Public Version Number

2

DI Record Publish Date

August 31, 2018

Package DI Number

10311917202423

Quantity per Package

24

Contains DI Package

00311917202426

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case