Duns Number:002348191
Device Description: ARROW(R) PICC powered by ARROW(R) VPS(R) Stylet
Catalog Number
CDA-35041-VPS
Brand Name
ARROW
Version/Model Number
IPN001327
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
K121941,K121941
Product Code
LJS
Product Code Name
Catheter,intravascular,therapeutic,long-term greater than 30 days
Public Device Record Key
30f34e58-c902-466b-a35d-b8472d9e7f25
Public Version Date
February 19, 2021
Public Version Number
5
DI Record Publish Date
August 15, 2017
Package DI Number
20801902126966
Quantity per Package
3
Contains DI Package
30801902126963
Package Discontinue Date
February 08, 2019
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 |