Duns Number:002348191
Device Description: Arrow-Howes(TM) Large-Bore Multi-Lumen Central Venous Catheterization Kit with Blue FlexTi Arrow-Howes(TM) Large-Bore Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter for High Volume Infusions
Catalog Number
AK-12123-F
Brand Name
ARROW
Version/Model Number
IPN036842
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
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K970864,K970864
Product Code
FOZ
Product Code Name
Catheter, intravascular, therapeutic, short-term less than 30 days
Public Device Record Key
7dad4687-8588-43df-a624-182633e36e64
Public Version Date
September 14, 2022
Public Version Number
6
DI Record Publish Date
December 14, 2018
Package DI Number
50801902121948
Quantity per Package
5
Contains DI Package
60801902121945
Package Discontinue Date
September 12, 2022
Package Status
Not 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 | 3195 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 13747 |
| 3 | A medical device with high risk that requires premarket approval | 3 |
| U | Unclassified | 26 |