Duns Number:002348191
Device Description: Single Shot Epidural Anesthesia Kit
Catalog Number
WA-02001
Brand Name
ARROW
Version/Model Number
IPN046774
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
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
-
Product Code
CAZ
Product Code Name
Anesthesia conduction kit
Public Device Record Key
0b0f3fd8-5002-4c0c-91e2-d6adae31cb62
Public Version Date
July 27, 2022
Public Version Number
6
DI Record Publish Date
November 07, 2018
Package DI Number
50801902014325
Quantity per Package
10
Contains DI Package
40801902014328
Package Discontinue Date
July 22, 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 |