Catalog Number

31439766

Brand Name

Kendall

Version/Model Number

31439766

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

July 01, 2023

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

DRX

Product Code Name

Electrode, electrocardiograph

Public Device Record Key

4e4f7d47-6444-499b-ad64-8876ef7666ce

Public Version Date

February 04, 2021

Public Version Number

6

DI Record Publish Date

September 24, 2016

Package DI Number

10884527008278

Quantity per Package

600

Contains DI Package

20884527008275

Package Discontinue Date

July 01, 2023

Package Status

In Commercial Distribution

Package Type

CASE