Horizon 3.0 Coil Holder

GUDID 05060229533012

THE MAGSTIM COMPANY LIMITED

Magnetic neural stimulation system
Primary Device ID05060229533012
NIH Device Record Key1980ef1b-0600-44d9-bb53-e60ad09feaa0
Commercial Distribution StatusIn Commercial Distribution
Brand NameHorizon 3.0 Coil Holder
Version Model Number5835-00-50
Company DUNS500375274
Company NameTHE MAGSTIM COMPANY LIMITED
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+441994241111
Emailsalesoperations@magstim.com
Phone+441994241111
Emailsalesoperations@magstim.com
Phone+441994241111
Emailsalesoperations@magstim.com
Phone+441994241111
Emailsalesoperations@magstim.com
Phone+441994241111
Emailsalesoperations@magstim.com
Phone+441994241111
Emailsalesoperations@magstim.com
Phone+441994241111
Emailsalesoperations@magstim.com
Phone+441994241111
Emailsalesoperations@magstim.com
Phone+441994241111
Emailsalesoperations@magstim.com
Phone+441994241111
Emailsalesoperations@magstim.com
Phone+441994241111
Emailsalesoperations@magstim.com
Phone+441994241111
Emailsalesoperations@magstim.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105060229533012 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OBPTranscranial Magnetic Stimulator

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-02-27
Device Publish Date2025-02-19

On-Brand Devices [Horizon 3.0 Coil Holder]

050602295326405630-00
050602295330125835-00-50

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