Catalog Number

IS5-90-30/A

Brand Name

Fountain®

Version/Model Number

00884450028230

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

-

Product Code

KRA

Product Code Name

Catheter, continuous flush

Public Device Record Key

f272114f-fca3-4b22-8078-6640d382d7dd

Public Version Date

June 10, 2022

Public Version Number

7

DI Record Publish Date

September 23, 2016

Package DI Number

10884450028237

Quantity per Package

5

Contains DI Package

00884450028230

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-