Duns Number:961027315
Device Description: PREOP PACK
Catalog Number
01-0914A
Brand Name
CARDINAL HEALTH
Version/Model Number
01-0914A
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
OJU
Product Code Name
Skin prep tray
Public Device Record Key
d87a8e82-6ea1-4de0-aee3-a318f99a5678
Public Version Date
June 17, 2022
Public Version Number
5
DI Record Publish Date
February 22, 2018
Package DI Number
50887488894827
Quantity per Package
30
Contains DI Package
10887488894829
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 | 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 |