Duns Number:002348191
Device Description: ARROW(R) FlexBlock Continuous Peripheral Nerve Block Set
Catalog Number
FB-19611-SST
Brand Name
ARROW
Version/Model Number
IPN046026
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
-
Product Code
CAZ
Product Code Name
Anesthesia conduction kit
Public Device Record Key
0a9670d5-ee1f-48d6-8248-1d1c9cd41c16
Public Version Date
August 15, 2022
Public Version Number
4
DI Record Publish Date
September 16, 2016
Package DI Number
30801902069208
Quantity per Package
10
Contains DI Package
00801902069207
Package Discontinue Date
August 01, 2022
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 |