Catalog Number

-

Brand Name

6750

Version/Model Number

Disposable ECG-EMG electrode

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

36ea1487-360b-4326-9984-f49dcaf4bea1

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

October 10, 2016

Package DI Number

00857398006288

Quantity per Package

25

Contains DI Package

10857398006117

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Bag