Duns Number:042763706
Device Description: PATIENT DRAPE FULL LENGTH 40X48 1/BAG 20/CASE STERILE
Catalog Number
0038901
Brand Name
ACE
Version/Model Number
0038901
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"
-
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
7b0a4433-2b87-40ea-8d4f-38cd9ee95652
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
October 21, 2015
Package DI Number
10614950000170
Quantity per Package
20
Contains DI Package
00614950000173
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Carton
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 1288 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 943 |
| U | Unclassified | 6 |