Duns Number:002348191
Device Description: Pressure Transduction Probe for use in conjunction with Arrow(R) Raulerson Spring-Wire Int Pressure Transduction Probe for use in conjunction with Arrow(R) Raulerson Spring-Wire Introduction Syringe
Catalog Number
AR-14703
Brand Name
ARROW
Version/Model Number
IPN032666
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
-
Product Code
DQX
Product Code Name
WIRE, GUIDE, CATHETER
Public Device Record Key
8adb3d27-bce9-49d4-8b87-db0016d96922
Public Version Date
January 25, 2021
Public Version Number
8
DI Record Publish Date
September 16, 2016
Package DI Number
20801902098188
Quantity per Package
25
Contains DI Package
00801902098184
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
| 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 |