Catalog Number

943685

Brand Name

Well at Walgreens

Version/Model Number

18704

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

Yes

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

K060145,K060145

Product Code

NUC

Product Code Name

Lubricant, Personal

Public Device Record Key

525a8f7f-6278-460a-879f-e8743b37d57c

Public Version Date

August 07, 2020

Public Version Number

7

DI Record Publish Date

November 16, 2016

Package DI Number

10311917187041

Quantity per Package

24

Contains DI Package

00311917187044

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case