Catalog Number

-

Brand Name

Codan

Version/Model Number

BC 231

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"

Yes

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

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

fdfe36c2-c58e-44cf-96b7-8b53908739df

Public Version Date

April 07, 2021

Public Version Number

4

DI Record Publish Date

May 31, 2017

Package DI Number

00813153021033

Quantity per Package

1

Contains DI Package

10813153021030

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-