Catalog Number

9231

Brand Name

Kendall

Version/Model Number

9231

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"

-

For Single-Use

Yes

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

KMF

Product Code Name

BANDAGE, LIQUID

Public Device Record Key

47f7d5f3-f8ec-4d68-8697-0105c4168d7f

Public Version Date

July 22, 2021

Public Version Number

9

DI Record Publish Date

April 27, 2015

Package DI Number

10884521024816

Quantity per Package

20

Contains DI Package

30884521024810

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE