Duns Number:341439008
Device Description: External Functional Neuromuscular Stimulator (8 channels), designed for use as stand-alone External Functional Neuromuscular Stimulator (8 channels), designed for use as stand-alone device as well as in combinationwith exercise equipment for walking and cycling applications, that has been validated for compatibility by HASOMED GmbH andshould be used under the supervision of a clinician. - manufactured for use in system
Catalog Number
FES01050
Brand Name
RehaStim 2
Version/Model Number
FES01050
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
-
Product Code
GZI
Product Code Name
Stimulator, Neuromuscular, External Functional
Public Device Record Key
37dbec03-1adb-43c0-9dbb-4a1fed8578a5
Public Version Date
July 06, 2018
Public Version Number
1
DI Record Publish Date
June 05, 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 | 2 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 6 |