Duns Number:175425982
Device Description: Latex Condom 3-ct
Catalog Number
08003
Brand Name
Kimono
Version/Model Number
MicroThin Large
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
b8598c36-ca84-44e5-a7f7-89eb52a22cfd
Public Version Date
November 11, 2020
Public Version Number
4
DI Record Publish Date
September 15, 2016
Package DI Number
10116169080030
Quantity per Package
8
Contains DI Package
20016169080030
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
MASTER CARTON
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 6 |
2 | A medical device with a moderate to high risk that requires special controls. | 6 |