Duns Number:002348191
Device Description: Arrow-Clark(TM) VectorFlow(TM) Antegrade Hemodialysis Catheter
Catalog Number
CS-15422-VFI
Brand Name
ARROW
Version/Model Number
IPN001388
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
K141051,K141051,K141051
Product Code
MSD
Product Code Name
Catheter, hemodialysis, implanted
Public Device Record Key
1a5812a8-528d-42a4-b7d5-f9371b103514
Public Version Date
August 31, 2022
Public Version Number
8
DI Record Publish Date
September 16, 2016
Package DI Number
40801902128681
Quantity per Package
1
Contains DI Package
30801902128684
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 | 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 |