Duns Number:320047483
Device Description: Venovo® Venous Stent System 20 mm x 160 mm (80 cm delivery catheter)
Catalog Number
VENUM20160
Brand Name
Venovo®
Version/Model Number
VENUM20160
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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"
Yes
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
QAN
Product Code Name
Stent, iliac vein
Public Device Record Key
108e8fbe-6f33-48dc-934b-3be54a4b4abc
Public Version Date
February 05, 2021
Public Version Number
2
DI Record Publish Date
March 18, 2019
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 32 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8 |
| 3 | A medical device with high risk that requires premarket approval | 174 |