Duns Number:002348191
Device Description: Two-Lumen Peripherally Inserted Central Catheter Kit with Blue FlexTip(R) Catheter, Placem Two-Lumen Peripherally Inserted Central Catheter Kit with Blue FlexTip(R) Catheter, Placement Wire and Maximal Barrier Precautions
Catalog Number
ASK-01552-DMI
Brand Name
ARROW
Version/Model Number
IPN034178
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
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K003006,K003006
Product Code
LJT
Product Code Name
PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR
Public Device Record Key
8d3b7e45-2fc9-4f43-992b-2a9943fe0eb5
Public Version Date
February 19, 2021
Public Version Number
6
DI Record Publish Date
October 16, 2015
Package DI Number
30801902093357
Quantity per Package
5
Contains DI Package
00801902093356
Package Discontinue Date
August 14, 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 |