Catalog Number

431612

Brand Name

Bard® Interglide™ Intermittent Catheter

Version/Model Number

431612

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

KOD

Product Code Name

CATHETER, UROLOGICAL

Public Device Record Key

a7b9b5c4-4f49-4731-9a4a-5eee04c6d485

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

July 23, 2016

Package DI Number

10801741078023

Quantity per Package

25

Contains DI Package

00801741078026

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA