Duns Number:022516829
Device Description: 6 mm X 30 mm
Catalog Number
SR-0630-CS
Brand Name
ENROUTE Transcarotid Stent
Version/Model Number
SR-0630-CS
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
P140026
Product Code
NIM
Product Code Name
Stent, Carotid
Public Device Record Key
3041d19c-14e8-4475-9625-6885e28a7971
Public Version Date
February 05, 2021
Public Version Number
5
DI Record Publish Date
July 28, 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. | 5 |
3 | A medical device with high risk that requires premarket approval | 18 |