Catalog Number

534696T

Brand Name

DUCOR

Version/Model Number

534696T

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

-

Product Code

DQO

Product Code Name

CATHETER, INTRAVASCULAR, DIAGNOSTIC

Public Device Record Key

a47e24a6-27bf-466b-be62-df9ddb24617c

Public Version Date

September 14, 2022

Public Version Number

5

DI Record Publish Date

August 01, 2016

Package DI Number

20705032014530

Quantity per Package

10

Contains DI Package

10705032014533

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX