Duns Number:372587696
Device Description: Partially Absorbable Hernia Repair Device
Catalog Number
UPLUG406
Brand Name
ULTRAPRO COMFORT PLUG
Version/Model Number
UPLUG406
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 22, 2020
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)
-
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
FTL
Product Code Name
Mesh, surgical, polymeric
Public Device Record Key
a44b2b3c-5ccc-479f-8a3d-3a4d984fb6a3
Public Version Date
June 10, 2022
Public Version Number
8
DI Record Publish Date
September 01, 2015
Package DI Number
20705031233246
Quantity per Package
6
Contains DI Package
10705031233249
Package Discontinue Date
May 22, 2020
Package Status
Not in Commercial Distribution
Package Type
BOX
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 84 |