Duns Number:080186051
Device Description: Angio Syringe with Handi-Fil Straw; fits injector: Angiomat Illumena
Catalog Number
-
Brand Name
LF
Version/Model Number
900101
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 04, 2018
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
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
DXT
Product Code Name
Injector And Syringe, Angiographic
Public Device Record Key
31ff7442-5590-467e-bc02-4d3baa682b7e
Public Version Date
January 05, 2022
Public Version Number
5
DI Record Publish Date
September 09, 2016
Package DI Number
20746190002335
Quantity per Package
50
Contains DI Package
10746190002338
Package Discontinue Date
June 04, 2018
Package Status
Not 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 | 31 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 75 |