Duns Number:021717889
Device Description: Console
Catalog Number
105650
Brand Name
AngioJet® Ultra 5000A
Version/Model Number
105650-001D
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
P980037,P980037,P980037,P980037,P980037,P980037,P980037,P980037,P980037
Product Code
MCX
Product Code Name
CATHETER, CORONARY, ATHERECTOMY
Public Device Record Key
5cecbb20-2e46-4402-a7fd-59dab01f6d1f
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 22, 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 | 536 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 8659 |
| 3 | A medical device with high risk that requires premarket approval | 1821 |
| U | Unclassified | 35 |