Duns Number:135741127
Device Description: Electrodes - Flex Plus -2.0" x 2.0" (1 pack = 4 electrodes per pack)
Catalog Number
ProM-022
Brand Name
Flex Plus
Version/Model Number
ProM-022
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)
Yes
Kit
-
Combination Product
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K132998,K132998
Product Code
GXY
Product Code Name
Electrode, Cutaneous
Public Device Record Key
8b4fe8a1-939d-4030-a5d3-dcb380af3866
Public Version Date
February 19, 2021
Public Version Number
4
DI Record Publish Date
July 26, 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. | 14 |