Duns Number:050636737
Device Description: Temporary non-roller type left heart support blood pump
Catalog Number
0550-0008
Brand Name
Impella
Version/Model Number
Impella 5.5 with SmartAssist Set, US
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)
Yes
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
P140003
Product Code
OZD
Product Code Name
Temporary Non-Roller Type Left Heart Support Blood Pump
Public Device Record Key
e3b8ee6f-7433-4626-b239-d82584a9c86e
Public Version Date
April 23, 2020
Public Version Number
1
DI Record Publish Date
April 15, 2020
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. | 16 |
3 | A medical device with high risk that requires premarket approval | 47 |