Duns Number:014464314
Catalog Number
-
Brand Name
E6330 Probe Cover, PE ,Gel and Elastic Bands 18x61cm - 7"x24"
Version/Model Number
E6330
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
-
Product Code
KKX
Product Code Name
Drape, Surgical
Public Device Record Key
d2a4f727-9b89-40a9-8c2a-2720f234cbad
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
November 20, 2016
Package DI Number
00816953027960
Quantity per Package
20
Contains DI Package
00816953027953
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Inner 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 |