Duns Number:014464314
Catalog Number
E233106N
Brand Name
E233106N Femoral Radial Angiography Drape 372x290cm
Version/Model Number
E233106N
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)
Yes
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
Yes
Prescription Use (Rx)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K101689,K101689
Product Code
KKX
Product Code Name
Drape, Surgical
Public Device Record Key
9e14e269-7405-43cd-a474-d421167989ab
Public Version Date
December 22, 2021
Public Version Number
6
DI Record Publish Date
October 10, 2016
Package DI Number
00816953020596
Quantity per Package
90
Contains DI Package
00816953020589
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 | 3 |
2 | A medical device with a moderate to high risk that requires special controls. | 489 |