Catalog Number

510689

Brand Name

GentleCath

Version/Model Number

510689

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

K213283,K213283,K213283

Product Code

GBM

Product Code Name

Catheter, Urethral

Public Device Record Key

daa0bdf7-18ef-4695-ace3-3b15e8d3b72e

Public Version Date

July 11, 2022

Public Version Number

1

DI Record Publish Date

July 01, 2022

Package DI Number

00768455196258

Quantity per Package

30

Contains DI Package

00768455196241

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Inner Carton