Duns Number:002348191
Device Description: Arterial Catheterization
Catalog Number
NA-04020-X1A
Brand Name
ARROW
Version/Model Number
IPN037108
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
K810675,K810675
Product Code
DQX
Product Code Name
WIRE, GUIDE, CATHETER
Public Device Record Key
326db6ac-d996-4d36-aecc-20f3b39675a1
Public Version Date
February 08, 2022
Public Version Number
8
DI Record Publish Date
July 08, 2017
Package DI Number
20801902119920
Quantity per Package
5
Contains DI Package
30801902119927
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 |