Taiwan FDA registration 1144c32506b83014b256cbf168e3d828
“HORIZON” repetitive Transcranial Magnetic Stimulator Therapy System
TW: “賀來悅”重覆式經顱磁刺激治療系統
Taiwan·Risk Class 2·MD·THE MAGSTIM COMPANY LIMITED·Registered Jul 17, 2023 – Jul 17, 2028ActiveRegistration details
- Analysis ID
- 1144c32506b83014b256cbf168e3d828
- License Form
- Ministry of Health Medical Device Import No. 036673
- Customs Code
- DHA05603667300
Company information
- Manufacturer
- THE MAGSTIM COMPANY LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- TRUSHINE MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K5805 Repetitive Transcranial Magnetic Stimulation (rTMS) Treatment System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 17, 2023
- Expiry Date
- Jul 17, 2028
About this record
Access comprehensive regulatory information for “HORIZON” repetitive Transcranial Magnetic Stimulator Therapy System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1144c32506b83014b256cbf168e3d828 and manufactured by THE MAGSTIM COMPANY LIMITED. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT CO., LTD..
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