Duns Number:134139174
Device Description: INSPIRIS RESILIA AORTIC VALVE
Catalog Number
11500A29
Brand Name
INSPIRIS RESILIA AORTIC VALVE
Version/Model Number
11500A
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
P150048
Product Code
LWR
Product Code Name
Heart-Valve, Non-Allograft Tissue
Public Device Record Key
f90b3192-14d3-49bb-95be-0746ac3a1481
Public Version Date
February 05, 2021
Public Version Number
5
DI Record Publish Date
July 31, 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 | 5 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 643 |
| 3 | A medical device with high risk that requires premarket approval | 212 |