Duns Number:002348191
Device Description: Two-Lumen Central Venous Catheterization Set with Blue FlexTip(R) Catheter
Catalog Number
CS-16702
Brand Name
ARROW
Version/Model Number
IPN036027
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
October 05, 2016
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
20418c5a-fb27-4374-8054-42444d2c867a
Public Version Date
February 19, 2021
Public Version Number
5
DI Record Publish Date
September 16, 2016
Package DI Number
40801935123004
Quantity per Package
5
Contains DI Package
10801934123004
Package Discontinue Date
October 05, 2016
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 |