Dual EMG Wet Gel Ag/AgCl Electrode

GUDID 00816271020322

Dual EMG Wet Gel Ag/AgCl Electrode Case 200 pcs per case

Noraxon U.S.A., Inc.

Kinesiology/electromyographic sensor set
Primary Device ID00816271020322
NIH Device Record Key7333efeb-9154-4903-9efa-e9c555c9427c
Commercial Distribution StatusIn Commercial Distribution
Brand NameDual EMG Wet Gel Ag/AgCl Electrode
Version Model Number272CASE
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100816271020322 [Primary]

FDA Product Code

HCCDevice, Biofeedback

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-08-31
Device Publish Date2020-08-21

Devices Manufactured by Noraxon U.S.A., Inc.

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00816271020780 - myoRESEARCH3 (MR3)2023-06-15 MR3 - myoVIDEO
00816271020797 - myoRESEARCH3 (MR3)2023-06-15 MR3 - myoPRESSURE
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