Catalog Number

-

Brand Name

DUREX Pleasure Pack Condom

Version/Model Number

Condom

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

HIS

Product Code Name

CONDOM

Public Device Record Key

bcad3fdb-8c7a-48ab-bd44-8e3049d17b8a

Public Version Date

July 27, 2020

Public Version Number

6

DI Record Publish Date

September 20, 2016

Package DI Number

20302340302191

Quantity per Package

6

Contains DI Package

10302340302194

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case