Duns Number:005146311
Device Description: Non-DEHP T-Connector Extension Set, T Housing, Retractable T-Connector, Injection Site
Catalog Number
2N3343
Brand Name
INTERLINK
Version/Model Number
2N3343
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
K921899,K921899
Product Code
FPA
Product Code Name
Set, administration, intravascular
Public Device Record Key
32a54c8d-0c97-49d9-a274-bcfad1e8ac5c
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
50085412004780
Quantity per Package
200
Contains DI Package
00085412004785
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 |