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“MAGSTIM” Repetitive transcranial magnetic stimulator (rTMS) System - Taiwan Registration 96d8ddd1de8dc9a7f010156ee279542f

Access comprehensive regulatory information for “MAGSTIM” Repetitive transcranial magnetic stimulator (rTMS) System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 96d8ddd1de8dc9a7f010156ee279542f and manufactured by THE MAGSTIM COMPANY LIMITED. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..

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96d8ddd1de8dc9a7f010156ee279542f
Registration Details
Taiwan FDA Registration: 96d8ddd1de8dc9a7f010156ee279542f
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Device Details

“MAGSTIM” Repetitive transcranial magnetic stimulator (rTMS) System
TW: “美格思錠”重覆式經顱磁刺激治療系統
Risk Class 2
MD

Registration Details

96d8ddd1de8dc9a7f010156ee279542f

Ministry of Health Medical Device Import No. 030972

DHA05603097206

Company Information

United Kingdom

Product Details

It is used to treat patients with severe depression who do not respond well to drug therapy, and those adult patients who do not improve during the medication phase.

K Devices for neuroscience

K5805 Repetitive Transcranial Magnetic Stimulation (rTMS) Treatment System

Imported from abroad

Dates and Status

Mar 27, 2018

Mar 27, 2028