Duns Number:961027315
Device Description: SPONGE GAUZE 2X2IN 3 PLY NONWOVEN ALL PURPOSE NONSTERILE
Catalog Number
C-NWS223
Brand Name
CARDINAL HEALTH
Version/Model Number
C-NWS223
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
December 31, 2023
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)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
NAB
Product Code Name
Gauze / sponge,nonresorbable for external use
Public Device Record Key
ba5d3cf7-194e-4d92-a141-6c6f8e966b3d
Public Version Date
February 24, 2022
Public Version Number
2
DI Record Publish Date
July 12, 2019
Package DI Number
50885380130913
Quantity per Package
25
Contains DI Package
20885380130912
Package Discontinue Date
December 31, 2023
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 | 101686 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 139430 |
| 3 | A medical device with high risk that requires premarket approval | 8 |
| U | Unclassified | 40 |