Catalog Number

-

Brand Name

Covidien

Version/Model Number

33145T

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 10, 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

c49e88ad-3bc7-4211-975d-2595daf8b8c4

Public Version Date

March 19, 2021

Public Version Number

3

DI Record Publish Date

September 30, 2016

Package DI Number

30817357020640

Quantity per Package

10

Contains DI Package

10817357020646

Package Discontinue Date

March 19, 2021

Package Status

Not in Commercial Distribution

Package Type

Box