Duns Number:219322575
Catalog Number
31-473670
Brand Name
ALLIANCE FEMORAL BROACH PROVISIONAL
Version/Model Number
31-473670
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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
-
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
HTQ
Product Code Name
BROACH
Public Device Record Key
794ff962-50d4-4b91-9fdf-a8b36de63d73
Public Version Date
February 07, 2019
Public Version Number
4
DI Record Publish Date
July 28, 2017
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 | 796 |
2 | A medical device with a moderate to high risk that requires special controls. | 137 |
3 | A medical device with high risk that requires premarket approval | 261 |