Duns Number:005146311
Device Description: Solution Set, Injection Site, Lever Lock Cannula, Male Luer Lock Adapter with Retractable Solution Set, Injection Site, Lever Lock Cannula, Male Luer Lock Adapter with Retractable Collar
Catalog Number
2C6402
Brand Name
INTERLINK
Version/Model Number
2C6402
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
K123868,K123868
Product Code
FPA
Product Code Name
Set, administration, intravascular
Public Device Record Key
0bd57cc8-f4df-44bf-a070-a11ba91fc5e7
Public Version Date
April 07, 2021
Public Version Number
5
DI Record Publish Date
September 24, 2016
Package DI Number
50085412002120
Quantity per Package
48
Contains DI Package
00085412002125
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 |