Catalog Number

239010NA

Brand Name

Actreen®

Version/Model Number

239010NA

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

GBM

Product Code Name

CATHETER, URETHRAL

Public Device Record Key

c918ce48-3d88-4016-8101-63c39083a00c

Public Version Date

June 03, 2022

Public Version Number

6

DI Record Publish Date

March 26, 2017

Package DI Number

04046964612886

Quantity per Package

18

Contains DI Package

04046964612879

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton