Catalog Number

6647WF

Brand Name

Kendall

Version/Model Number

6647WF

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

KGX

Product Code Name

Tape and bandage, adhesive

Public Device Record Key

68635e26-0b3a-4941-9635-8d5f0f67fd35

Public Version Date

December 22, 2021

Public Version Number

3

DI Record Publish Date

June 27, 2018

Package DI Number

30884521175772

Quantity per Package

80

Contains DI Package

10884521175778

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE