Duns Number:025460908
Device Description: NF CONNECTOR, NEUTRAL DISPLACEMENT
Catalog Number
DYNDTNV200
Brand Name
MEDLINE
Version/Model Number
DYNDTNV200
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
42b96c13-533e-4487-88cb-0e6dfdf8ec69
Public Version Date
April 07, 2021
Public Version Number
2
DI Record Publish Date
April 16, 2020
Package DI Number
20193489194200
Quantity per Package
200
Contains DI Package
10193489194203
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 | 38540 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 85094 |
| 3 | A medical device with high risk that requires premarket approval | 2 |
| U | Unclassified | 7 |