Duns Number:035596579
Device Description: e-vive II NMES System with Post-Op Brace; L/XL, Left (ITALIAN)
Catalog Number
CY-1000-311I
Brand Name
e-vive II NMES System with Post-Op Brace; L/XL, Left (ITALIAN)
Version/Model Number
CY-1000-311I
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
-
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
-
Product Code
GZJ
Product Code Name
Stimulator, Nerve, Transcutaneous, For Pain Relief
Public Device Record Key
d733a574-593f-41b5-9fc5-f0b18c7e4b92
Public Version Date
February 19, 2021
Public Version Number
2
DI Record Publish Date
January 04, 2021
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 | 90 |
2 | A medical device with a moderate to high risk that requires special controls. | 91 |