Catalog Number

-

Brand Name

United Urologics Closed System Catheter

Version/Model Number

UU16R

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

November 15, 2019

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)

Yes

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

KOD

Product Code Name

Catheter, Urological

Public Device Record Key

71a3d7cc-e4d7-43ba-9bf7-759e51e0acb1

Public Version Date

November 18, 2019

Public Version Number

3

DI Record Publish Date

March 22, 2017

Package DI Number

10818016020106

Quantity per Package

100

Contains DI Package

00818016020635

Package Discontinue Date

November 15, 2019

Package Status

Not in Commercial Distribution

Package Type

-