Duns Number:964569052
Device Description: STARCLOSE SE Vascular Closure System
Catalog Number
14679-01
Brand Name
STARCLOSE SE
Version/Model Number
14679-01
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
-
Product Code
MGB
Product Code Name
DEVICE, HEMOSTASIS, VASCULAR
Public Device Record Key
bbaf5a8c-6249-4a26-878d-ce1071c48426
Public Version Date
October 21, 2020
Public Version Number
5
DI Record Publish Date
November 21, 2014
Package DI Number
28717648079461
Quantity per Package
10
Contains DI Package
08717648079467
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 3 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 964 |
| 3 | A medical device with high risk that requires premarket approval | 775 |