Taiwan FDA registration 1be4a3a3c033c1e4117f5ee138bf9c47

"Meige Meichu" Meige Weida transcranial magnetic stimulation treatment system and accessories

TW: “美葛梅丘”美葛偉達經顱磁刺激治療系統及附件
Taiwan flagTaiwan·Risk Class 2·Tonic Elektronik A/S·Registered Jan 18, 2020 – Jan 18, 2030Active
Registration details
Analysis ID
1be4a3a3c033c1e4117f5ee138bf9c47
Customs Code
DHA05603316505
Company information
Manufacturer Country
Denmark
Authorized Representative
CHANCELLOR INSTRUMENT CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
K Neuroscience
Product Type (Level 2)
K.5805 重複式經顱磁刺激(rTMS)治療系統
Import Information
import
Dates and status
Registration Date
Jan 18, 2020
Expiry Date
Jan 18, 2030
About this record

Access comprehensive regulatory information for "Meige Meichu" Meige Weida transcranial magnetic stimulation treatment 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 1be4a3a3c033c1e4117f5ee138bf9c47 and manufactured by Tonic Elektronik A/S. The authorized representative in Taiwan is CHANCELLOR INSTRUMENT CO., 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