Catalog Number

6392

Brand Name

MC3

Version/Model Number

6392

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K132451,K132451,K132451

Product Code

DWF

Product Code Name

Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

Public Device Record Key

cf3ba00a-817d-47fa-86e7-b206279b247c

Public Version Date

August 05, 2022

Public Version Number

4

DI Record Publish Date

January 10, 2018

Package DI Number

20854916006694

Quantity per Package

10

Contains DI Package

10854916006680

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-