Catalog Number

-

Brand Name

CareFusion

Version/Model Number

2009101-210

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"

Yes

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

K040784,K040784,K040784

Product Code

DRX

Product Code Name

Electrode, Electrocardiograph

Public Device Record Key

b5d85f51-a14c-4b0c-92d1-9673abe20454

Public Version Date

July 06, 2018

Public Version Number

2

DI Record Publish Date

May 10, 2018

Package DI Number

28809083941356

Quantity per Package

5000

Contains DI Package

18809083941359

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton Box