Duns Number:066689993
Device Description: BODYMED IONTOPHORESIS, ELECTRODES MEDIUM 3.25" X 3.25", 12/BOX
Catalog Number
ZZAI325
Brand Name
BodyMed
Version/Model Number
ZZAI325
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
K080580
Product Code
EGJ
Product Code Name
Device, Iontophoresis, Other Uses
Public Device Record Key
9b2d3dff-3d80-4084-83fd-3137130e4fc1
Public Version Date
February 27, 2020
Public Version Number
2
DI Record Publish Date
December 27, 2018
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 | 3 |
2 | A medical device with a moderate to high risk that requires special controls. | 23 |