Duns Number:023904428
Device Description: Impervious U-Drape 4 IN x 21 IN SPLIT 60 in x 70 in
Catalog Number
-
Brand Name
McKesson
Version/Model Number
183-i80-09106-S
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)
-
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
4d9901c9-2721-4f61-bf8f-50cdf6841607
Public Version Date
December 22, 2021
Public Version Number
4
DI Record Publish Date
July 09, 2018
Package DI Number
40612479230475
Quantity per Package
30
Contains DI Package
10612479230467
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 | 870 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 422 |
| U | Unclassified | 44 |