Duns Number:967358115
Catalog Number
VH0808040
Brand Name
GORE VIABIL Biliary Endoprosthesis
Version/Model Number
VH0808040
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"
-
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
K081184
Product Code
FGE
Product Code Name
Catheter, Biliary, Diagnostic
Public Device Record Key
737c188d-fd22-4776-b660-29d80fc49a3b
Public Version Date
July 22, 2021
Public Version Number
6
DI Record Publish Date
March 07, 2016
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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 561 |
3 | A medical device with high risk that requires premarket approval | 623 |