Catalog Number

-

Brand Name

McKesson

Version/Model Number

8906

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

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

LRO

Product Code Name

General Surgery Tray

Public Device Record Key

e3db77c5-8f76-4a45-89b5-880285c6ebac

Public Version Date

June 17, 2022

Public Version Number

3

DI Record Publish Date

February 14, 2020

Package DI Number

40612479251951

Quantity per Package

50

Contains DI Package

10612479251943

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case