Duns Number:809699023
Device Description: NAMIC Vented 72" Fluid Delivery Set with Macro Drip Chamber with 15 Micron Filter
Catalog Number
-
Brand Name
NAMIC
Version/Model Number
80029130
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
a683376f-bebf-45e7-99a3-ce59fb477312
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
September 17, 2015
Package DI Number
H965800291301
Quantity per Package
150
Contains DI Package
H965800291300
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
BOX
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 71 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1641 |