6 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: Class Ii
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Magstim Rapid Therapy System consisting of: Rapid Mainframe, Rapid Single Power Supply Unit , Rapid User Interface, Air Film Coil and Main Filters Product Usage For the treatment of major depressive disorders in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.
FDA Enforcement
Class II
·Terminated·The Magstim Company Limited·April 18, 2018
HORIZON Ez Arm (Part of the HORIZON TMS Therapy System.)
FDA Enforcement
Class II
·Ongoing·The Magstim Company Limited·February 20, 2019
Neurosign 100, Product Number 9883-01. Intraoperative Nerve Monitor - Product Usage: indicated for use in stimulating and monitoring cranial motor nerves, especially the facial nerve (VII), during ENT surgical procedures.
FDA Enforcement
Class II
·Terminated·The Magstim Company Limited·January 27, 2021
Neurosign V4 Intraoperative Nerve monitor family of devices.
FDA Enforcement
Class II
·Terminated·The Magstim Company Limited·September 2, 2020
Horizon PSU Stim Interconnecting Cable - Product Usage: Horizon is indicated for the treatment of Major Depressive Disorder in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.
FDA Enforcement
Class II
·Terminated·The Magstim Company Limited·May 20, 2020
Rapid2 PSU Stim Interconnecting Cable - Product Usage: indicated for the treatment of Major Depressive Disorder in adult patients who have failed to achieve satisfactory improvement from prior antidepressant medication in the current episode.
FDA Enforcement
Class II
·Terminated·The Magstim Company Limited·May 20, 2020