Catalog Number

-

Brand Name

McKesson

Version/Model Number

176-5728

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

NEC

Product Code Name

Bandage, Liquid, Skin Protectant

Public Device Record Key

b6b3aa93-8832-42a8-98e1-aa88e82f0bf2

Public Version Date

April 12, 2019

Public Version Number

1

DI Record Publish Date

April 04, 2019

Package DI Number

00612479228283

Quantity per Package

100

Contains DI Package

00612479226951

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case