Duns Number:401020409
Catalog Number
OJG10DST12
Brand Name
ENDOFLOW II - PROBES - 16 holes diam 10i inch
Version/Model Number
OJG10DST12
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
GBX
Product Code Name
Catheter, Irrigation
Public Device Record Key
accbc99e-599a-411e-8b3d-21be7dbea4a6
Public Version Date
April 23, 2019
Public Version Number
4
DI Record Publish Date
October 11, 2016
Package DI Number
03700512920304
Quantity per Package
6
Contains DI Package
03700512910305
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box label 2
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 64 |
2 | A medical device with a moderate to high risk that requires special controls. | 152 |