Catalog Number

-

Brand Name

Tab Electrodes

Version/Model Number

7126

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)

-

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

9dc54331-729e-48fe-8680-774586d4a1b6

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

November 29, 2016

Package DI Number

00616784712635

Quantity per Package

10

Contains DI Package

00616784712628

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-