Duns Number:002348191
Device Description: Large-Bore Multi-Lumen Central Venous Catheterization Set with Blue FlexTip(R) Catheter fo Large-Bore Multi-Lumen Central Venous Catheterization Set with Blue FlexTip(R) Catheter for High Volume Infusions
Catalog Number
CS-12123-F
Brand Name
ARROW
Version/Model Number
IPN030068
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
K862056,K862056
Product Code
DQY
Product Code Name
Catheter, percutaneous
Public Device Record Key
64cc5979-3047-48f5-aa61-31270baa1bf1
Public Version Date
September 22, 2022
Public Version Number
6
DI Record Publish Date
June 26, 2018
Package DI Number
10801902097054
Quantity per Package
5
Contains DI Package
20801902097051
Package Discontinue Date
September 15, 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 |