Catalog Number

-

Brand Name

Walgreens

Version/Model Number

749215

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

ITJ

Product Code Name

Walker, Mechanical

Public Device Record Key

f77ec995-06f6-4e7a-9ff0-412d73d647f5

Public Version Date

November 09, 2020

Public Version Number

1

DI Record Publish Date

November 01, 2020

Package DI Number

10311917214976

Quantity per Package

12

Contains DI Package

00311917214979

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case