Catalog Number

-

Brand Name

McKesson

Version/Model Number

153-152

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LRJ

Product Code Name

Disinfectant, Medical Devices

Public Device Record Key

c9524ea1-9d53-425f-bbf8-15704b245981

Public Version Date

March 19, 2021

Public Version Number

4

DI Record Publish Date

March 22, 2019

Package DI Number

00612479225824

Quantity per Package

4

Contains DI Package

00612479225817

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case