Duns Number:421340711
Catalog Number
-
Brand Name
Disposable Electrode Serie
Version/Model Number
VIS-F005-SG032
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K091672,K091672,K091672
Product Code
GEI
Product Code Name
Electrosurgical, Cutting & Coagulation & Accessories
Public Device Record Key
e901e983-7b48-4f63-a163-2faa908d7a90
Public Version Date
February 07, 2019
Public Version Number
4
DI Record Publish Date
July 21, 2017
Package DI Number
06924274955627
Quantity per Package
300
Contains DI Package
06924274955610
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 171 |