Duns Number:080935429
Device Description: Needleless Connector Neutral Displacement Valve with 6 IN (15.2 cm) Extension Set
Catalog Number
2001NP
Brand Name
Kendall
Version/Model Number
2001NP
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"
-
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
41c3930f-111f-4fcc-bf94-1f2237d7841e
Public Version Date
October 12, 2020
Public Version Number
7
DI Record Publish Date
September 24, 2016
Package DI Number
20884521533001
Quantity per Package
100
Contains DI Package
10884521533004
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 | 672 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1692 |
| U | Unclassified | 17 |