Duns Number:002348191
Device Description: SureBlock(R) Spinal Anesthesia Kit with 0.75% Bupivacaine and 8.25% Dextrose
Catalog Number
ASK-24090-SA
Brand Name
ARROW
Version/Model Number
IPN922632
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"
-
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
K911260,K911260
Product Code
BSP
Product Code Name
NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)
Public Device Record Key
fa3e100d-34da-4944-9d4f-2522131f6831
Public Version Date
October 17, 2022
Public Version Number
2
DI Record Publish Date
August 24, 2021
Package DI Number
20801902202288
Quantity per Package
5
Contains DI Package
10801902202281
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 |