Magstim Rapid² Therapy System User Interface

GUDID 05060229531933

THE MAGSTIM COMPANY LIMITED

Magnetic neural stimulation system, stationary
Primary Device ID05060229531933
NIH Device Record Key4aeb5b1f-a1f1-48a0-a3d7-d5c973cd82d7
Commercial Distribution StatusIn Commercial Distribution
Brand NameMagstim Rapid² Therapy System User Interface
Version Model Number3022-00T
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 Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+441994240798
EmailQA.RA@magstim.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105060229531933 [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 StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-23

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05060229533036 - Horizon 3.0 ez Cool Coil 2024-05-17 Horizon 3.0 ez Cool Coil
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05060229532930 - StimGuide Pro Head Reference2024-01-09 StimGuide Pro Head Reference
05060229532947 - StimGuide Pro MT Coil Tracker Tool2024-01-09 StimGuide Pro MT Coil Tracker Tool

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