Catalog Number

-

Brand Name

Walgreens

Version/Model Number

725823

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)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

FNY

Product Code Name

Basin, Emesis

Public Device Record Key

fe40a7c5-0952-40b7-8417-989f00026c9d

Public Version Date

March 30, 2020

Public Version Number

1

DI Record Publish Date

March 20, 2020

Package DI Number

10311917214747

Quantity per Package

30

Contains DI Package

00311917214740

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Pack