Catalog Number

-

Brand Name

Codan

Version/Model Number

A 602

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

464eb464-0bbb-4971-8b00-5274cbcba749

Public Version Date

April 07, 2021

Public Version Number

4

DI Record Publish Date

October 21, 2016

Package DI Number

813153020821

Quantity per Package

1

Contains DI Package

10813153020828

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-