Catalog Number

-

Brand Name

McKesson

Version/Model Number

30321

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"

Yes

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

-

Product Code

LRR

Product Code Name

First Aid Kit With Drug

Public Device Record Key

91bb0e94-a8bb-431a-b4fc-90a9c3fe10e9

Public Version Date

June 29, 2022

Public Version Number

1

DI Record Publish Date

June 21, 2022

Package DI Number

00612479257542

Quantity per Package

12

Contains DI Package

00612479257535

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case