Duns Number:180572216
Device Description: Safety Huber Infusion Set, non-coring, 20G X 3/4, 7"tube
Catalog Number
37855
Brand Name
EXEL SecureTouch Safety Huber Infusion Set
Version/Model Number
37855
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"
Yes
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
FPA
Product Code Name
Set, Administration, Intravascular
Public Device Record Key
5586dffb-db56-46a1-9a12-735d3d96c063
Public Version Date
October 23, 2019
Public Version Number
3
DI Record Publish Date
September 23, 2016
Package DI Number
30020221378550
Quantity per Package
8
Contains DI Package
10020221378556
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 21 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 82 |