Catalog Number

-

Brand Name

Codan

Version/Model Number

BC 2003

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

10f6cc94-c6f9-4d55-b0af-5f2c864d6f20

Public Version Date

October 23, 2019

Public Version Number

3

DI Record Publish Date

September 20, 2016

Package DI Number

897891001748

Quantity per Package

1

Contains DI Package

10897891001745

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-