Duns Number:342397433
Device Description: Single Use Medical Device for Ophthalmic Surgery
Catalog Number
E7930
Brand Name
BIPOL.PEN 23G TPD LEMO 12/BX
Version/Model Number
E7930
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
GXI
Product Code Name
Probe, Radiofrequency Lesion
Public Device Record Key
a9d5ad8f-8eef-4a77-8dab-a6e908f3cd2c
Public Version Date
October 29, 2018
Public Version Number
4
DI Record Publish Date
July 15, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 11 |