Taiwan FDA registration 0a7e9c1e3d25e62c80049d7c503cf249
“Brainsway” Deep TMS System and Accessories
TW: “智道”重複式經顱磁刺激治療系統及配件
Taiwan·Risk Class 2·MD·Brainsway Ltd.·Registered Apr 16, 2021 – Apr 16, 2026ExpiredRegistration details
- Analysis ID
- 0a7e9c1e3d25e62c80049d7c503cf249
- License Form
- Ministry of Health Medical Device Import No. 034433
- Customs Code
- DHA05603443309
Company information
- Manufacturer
- Brainsway Ltd.
- Manufacturer Country
- Israel
- Authorized Representative
- UNISON COMPANY LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K5805 Repetitive Transcranial Magnetic Stimulation (rTMS) Treatment System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 16, 2021
- Expiry Date
- Apr 16, 2026
About this record
Access comprehensive regulatory information for “Brainsway” Deep TMS System and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0a7e9c1e3d25e62c80049d7c503cf249 and manufactured by Brainsway Ltd.. The authorized representative in Taiwan is UNISON COMPANY LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices