Duns Number:025460908
Device Description: IV EXT SET, 8", 0.4ML,NF TPORT, NF VALVE
Catalog Number
DYNDTC5082
Brand Name
Medline
Version/Model Number
DYNDTC5082
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
0a2bdc7b-ebda-4226-b7ce-574d28ddb0d1
Public Version Date
November 29, 2021
Public Version Number
4
DI Record Publish Date
November 07, 2016
Package DI Number
40884389714769
Quantity per Package
100
Contains DI Package
10884389714768
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
| 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 |