Catalog Number

-

Brand Name

Walgreens

Version/Model Number

7W926

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

K012203,K012203

Product Code

NUC

Product Code Name

Lubricant, Personal

Public Device Record Key

82eef9bf-d353-4eae-92d9-1e0492a0cfe4

Public Version Date

February 06, 2020

Public Version Number

1

DI Record Publish Date

January 29, 2020

Package DI Number

10311917206551

Quantity per Package

72

Contains DI Package

00311917206554

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

shipper