Catalog Number

-

Brand Name

DUREX Invisible 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

53fe8f48-e199-4c2a-8120-a03b1c751a04

Public Version Date

December 13, 2018

Public Version Number

4

DI Record Publish Date

September 20, 2016

Package DI Number

20302340912772

Quantity per Package

16

Contains DI Package

10302340912775

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case