Catalog Number

-

Brand Name

McKesson

Version/Model Number

2069

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

ITG

Product Code Name

Bandage, Cast

Public Device Record Key

745ff2ec-04a3-4705-819c-319c8a27c16d

Public Version Date

December 08, 2021

Public Version Number

3

DI Record Publish Date

July 15, 2020

Package DI Number

20612479192663

Quantity per Package

12

Contains DI Package

10612479192659

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box