Catalog Number

7140C

Brand Name

Kendall

Version/Model Number

7140C

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 22, 2021

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

463cb544-40a8-4a20-bcfc-683fa0b2c1fe

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

June 29, 2018

Package DI Number

20884521175348

Quantity per Package

40

Contains DI Package

10884521175341

Package Discontinue Date

February 22, 2021

Package Status

Not in Commercial Distribution

Package Type

CASE