Catalog Number

55544P

Brand Name

Kendall

Version/Model Number

55544P

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

NAD

Product Code Name

Dressing, wound, occlusive

Public Device Record Key

e107f6a4-f233-45c8-b614-3b8235b8b337

Public Version Date

July 22, 2021

Public Version Number

4

DI Record Publish Date

June 30, 2018

Package DI Number

30884521020829

Quantity per Package

50

Contains DI Package

10884521020825

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE