Catalog Number

-

Brand Name

DUREX Extra Sensitive 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

K980319,K980319,K980319,K980319

Product Code

HIS

Product Code Name

CONDOM

Public Device Record Key

870c218c-cd90-4e3e-9f9f-87fb9773d2fd

Public Version Date

October 17, 2019

Public Version Number

6

DI Record Publish Date

September 20, 2016

Package DI Number

20302340129002

Quantity per Package

24

Contains DI Package

10302340129005

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case