Catalog Number

8887660143

Brand Name

Dover

Version/Model Number

8887660143

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)

Yes

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

ff9fc211-fdf5-4dc0-bbd3-60c93b27368d

Public Version Date

June 19, 2020

Public Version Number

7

DI Record Publish Date

September 24, 2016

Package DI Number

20884521019789

Quantity per Package

100

Contains DI Package

10884521019782

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE