Duns Number:066689993
Device Description: BODYMED TENS/EMS/MASSAGER COMBO WITH BODY PART DIAGRAM
Catalog Number
ZZACOMBOBDPT1
Brand Name
BodyMed
Version/Model Number
ZZACOMBOBDPT1
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
-
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
K181688,K181688,K181688
Product Code
GZJ
Product Code Name
Stimulator, Nerve, Transcutaneous, For Pain Relief
Public Device Record Key
8ea7886b-e7f6-4470-9bd9-cbd71e33474a
Public Version Date
February 19, 2021
Public Version Number
5
DI Record Publish Date
October 31, 2019
Package DI Number
20815991023020
Quantity per Package
32
Contains DI Package
10815991023023
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Master Carton
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 |