Duns Number:961027315
Device Description: DEVICE
Catalog Number
SAN31DVEV2
Brand Name
CARDINAL HEALTH
Version/Model Number
SAN31DVEV2
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
OEQ
Product Code Name
Angiography/angioplasty kit
Public Device Record Key
8ff45768-28e1-453d-b22d-0ffbd1e66f65
Public Version Date
September 10, 2018
Public Version Number
1
DI Record Publish Date
August 08, 2018
Package DI Number
50888439124062
Quantity per Package
5
Contains DI Package
10888439124064
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 |