EverEx Rehab

GUDID 08809970060005

EverEx

Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation software
Primary Device ID08809970060005
NIH Device Record Keybbfde762-b77f-4224-8918-dea854c521a5
Commercial Distribution StatusIn Commercial Distribution
Brand NameEverEx Rehab
Version Model Number1.1.0
Company DUNS695651100
Company NameEverEx
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Safe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108809970060005 [Primary]

FDA Product Code

QKCInteractive Rehabilitation Exercise Device, Prescription Use

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-04-11
Device Publish Date2024-04-03

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