mTrigger

GUDID 00863712000306

Analytical non-scalp cutaneous electrode

Primary Device ID	00863712000306
NIH Device Record Key	50b74505-fa41-4c17-b356-2ed759eab226
Commercial Distribution Status	In Commercial Distribution
Brand Name	mTrigger
Version Model Number	AE2403
Company DUNS	080226941
Company Name	MTRIGGER, LLC
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	true

Device Issuing Agency	Device ID
GS1	00863712000306 [Primary]

DRX	Electrode, Electrocardiograph

Steralize Prior To Use	false
Device Is Sterile	false

00863712000306	Cutaneous sensing electrode - 4-pack
00863712000337	mTrigger Biofeedback System

Mark Image Registration \| Serial	Company Trademark Application Date
MTRIGGER 87094527 5424174 Live/Registered	mTrigger, LLC 2016-07-06