Duns Number:002348191
Device Description: ARROW(R) UltraQuik(R) Ultrasound Peripheral Nerve Block Needle
Catalog Number
AB-21150-US
Brand Name
ARROW
Version/Model Number
IPN045598
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
CAZ
Product Code Name
Anesthesia conduction kit
Public Device Record Key
bc0af608-2eb0-4685-ab5c-7b8d6a7d705d
Public Version Date
September 03, 2021
Public Version Number
7
DI Record Publish Date
September 16, 2016
Package DI Number
30801902077838
Quantity per Package
25
Contains DI Package
00801902077837
Package Discontinue Date
September 02, 2021
Package Status
Not 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 |