Duns Number:096372255
Device Description: Bifurcated 72" IV Set, Vented Bulk NS
Catalog Number
-
Brand Name
DeRoyal
Version/Model Number
35-530003
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)
-
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
d1eaf813-f4cd-476b-b5b7-2f1268bd8ca2
Public Version Date
April 07, 2021
Public Version Number
4
DI Record Publish Date
September 12, 2016
Package DI Number
50749756787630
Quantity per Package
50
Contains DI Package
00749756787635
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 | 7041 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 4913 |
| U | Unclassified | 3 |