Duns Number:002348191
Device Description: Maximal Barrier Precautions for High Volume Infusions. You-Bend(TM) Two-Lumen Hemodialysi Maximal Barrier Precautions for High Volume Infusions. You-Bend(TM) Two-Lumen Hemodialysis Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue(R) Catheter, Sharps Safety Features and Maximal Barrier Precautions for High Volume
Catalog Number
CDA-23122-U1A
Brand Name
ARROW
Version/Model Number
IPN032972
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
K993933,K993933
Product Code
MPB
Product Code Name
CATHETER, HEMODIALYSIS, NON-IMPLANTED
Public Device Record Key
b893b2bc-8126-4a40-b05c-801a416a4d75
Public Version Date
February 05, 2021
Public Version Number
5
DI Record Publish Date
February 03, 2017
Package DI Number
30801902096174
Quantity per Package
5
Contains DI Package
00801902096173
Package Discontinue Date
September 27, 2018
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 |