Duns Number:961027315
Device Description: COURTESY PK TIE TO SAN43PMMFJ
Catalog Number
SID43DPMFA
Brand Name
CARDINAL HEALTH
Version/Model Number
SID43DPMFA
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
KKX
Product Code Name
Drape, surgical
Public Device Record Key
17f1484a-f765-401e-b95d-1710b38aefc7
Public Version Date
June 17, 2022
Public Version Number
6
DI Record Publish Date
May 25, 2017
Package DI Number
50887488702689
Quantity per Package
20
Contains DI Package
10887488702681
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 |