Catalog Number

-

Brand Name

Mckesson

Version/Model Number

30323

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

14b545a2-6451-42e5-8d6d-f7ac7e96f761

Public Version Date

December 02, 2020

Public Version Number

1

DI Record Publish Date

November 24, 2020

Package DI Number

00612479257580

Quantity per Package

6

Contains DI Package

00612479257573

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case