Duns Number:809699023
Device Description: NAMIC Angiographic 12 ml Control Syringe
Catalog Number
-
Brand Name
NAMIC
Version/Model Number
80087003
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
4efdd293-fc17-4720-a38d-04390cc53fd9
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
September 17, 2015
Package DI Number
H749800870031
Quantity per Package
50
Contains DI Package
H749800870030
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
BOX
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 71 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1641 |