MyoMotion

GUDID 00816271020247

Research Sensor

Noraxon U.S.A., Inc.

Kinesiology/electromyographic sensor set
Primary Device ID00816271020247
NIH Device Record Key4a6b5f66-a6b4-46be-b278-fff3a7f484b0
Commercial Distribution StatusIn Commercial Distribution
Brand NameMyoMotion
Version Model Number610
Company DUNS611243809
Company NameNoraxon U.S.A., Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone4804433413
Emailsupport@noraxon.com

Operating and Storage Conditions

Handling Environment TemperatureBetween -40 Degrees Celsius and 70 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS100816271020247 [Primary]

FDA Product Code

KQXGoniometer, Ac-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-11-29
Device Publish Date2019-11-21

On-Brand Devices [MyoMotion]

00816271020308MyoMotion Clinical Receiver
00816271020285Clinical Sensor
00816271020261MyoMotion Sensor Charging Station
00816271020254MyoMotion Research Pro Receiver
00816271020247Research Sensor

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