DIERS iEMG

GUDID 04260242060200

Electromyography monitor

Primary Device ID	04260242060200
NIH Device Record Key	c3d59513-e11e-4bdf-b1cc-78af62905c44
Commercial Distribution Status	In Commercial Distribution
Brand Name	DIERS iEMG
Version Model Number	n/a
Company DUNS	499189983
Company Name	DIERS International GmbH
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	false
Lot Batch	false
Serial Number	true
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	04260242060200 [Primary]

HCC	Device, Biofeedback

Steralize Prior To Use	false
Device Is Sterile	false