Duns Number:514029771
Catalog Number
-
Brand Name
Disposable Adhesive Surface Electrodes
Version/Model Number
TEON1F5045
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
K120494,K120494
Product Code
GXY
Product Code Name
Electrode, Cutaneous
Public Device Record Key
ace81b6f-bd7c-4b40-a125-f4f0dcfd7a11
Public Version Date
July 06, 2018
Public Version Number
4
DI Record Publish Date
June 21, 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 |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 1 |
2 | A medical device with a moderate to high risk that requires special controls. | 22 |