Duns Number:002348191
Device Description: Three-Lumen CVC
Catalog Number
CS-12553-J
Brand Name
ARROW
Version/Model Number
IPN033015
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
a5d334e0-4717-4ee1-8096-03a4fd7e2531
Public Version Date
October 01, 2021
Public Version Number
5
DI Record Publish Date
June 05, 2018
Package DI Number
20801913122896
Quantity per Package
5
Contains DI Package
30801913122893
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 |