Catalog Number

-

Brand Name

Covidien

Version/Model Number

33145

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 31, 2019

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

IKD

Product Code Name

Cable, Electrode

Public Device Record Key

25dde745-26ee-491a-8bce-36e47f0b6401

Public Version Date

March 19, 2021

Public Version Number

3

DI Record Publish Date

September 24, 2016

Package DI Number

50817357022075

Quantity per Package

10

Contains DI Package

30817357022071

Package Discontinue Date

March 19, 2021

Package Status

Not in Commercial Distribution

Package Type

Case