Catalog Number

-

Brand Name

CURE ULTRAPLUS CATHETER

Version/Model Number

ULTRAPlus10

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K080881,K080881,K080881

Product Code

KOD

Product Code Name

Catheter, Urological

Public Device Record Key

cd400e84-c23f-45ce-82db-0d460d737aae

Public Version Date

October 19, 2022

Public Version Number

2

DI Record Publish Date

April 19, 2022

Package DI Number

10815947021349

Quantity per Package

30

Contains DI Package

00815947021342

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Carton