Duns Number:005146311
Device Description: One-Link Non-DEHP 3 Lead Standard Bore Catheter Extension Set Bonded Needle-free IV Connec One-Link Non-DEHP 3 Lead Standard Bore Catheter Extension Set Bonded Needle-free IV Connector with Neutral Fluid Displacement
Catalog Number
7N8334K
Brand Name
ONE-LINK
Version/Model Number
7N8334K
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
K132734,K132734
Product Code
FPA
Product Code Name
Set, administration, intravascular
Public Device Record Key
c6916a51-6248-4930-bd57-406f16cae8b9
Public Version Date
October 19, 2022
Public Version Number
3
DI Record Publish Date
May 22, 2018
Package DI Number
50085412613487
Quantity per Package
200
Contains DI Package
00085412613482
Package Discontinue Date
-
Package Status
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 | 3 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 358 |