Taiwan FDA registration 6946b0365271473b6f660a1398fed0e2
“Deymed” repetitive Transcranial Magnetic Stimulator Therapy System
TW: “萬美德”重覆式經顱磁刺激治療系統
Taiwan·Risk Class 2·MD·Deymed Diagnostic s.r.o.·Registered Jan 03, 2022 – Jan 03, 2027ActiveRegistration details
- Analysis ID
- 6946b0365271473b6f660a1398fed0e2
- License Form
- Ministry of Health Medical Device Import No. 035167
- Customs Code
- DHA05603516706
Company information
- Manufacturer
- Deymed Diagnostic s.r.o.
- Manufacturer Country
- Czechia
- Authorized Representative
- Onemed 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
- Jan 03, 2022
- Expiry Date
- Jan 03, 2027
About this record
Access comprehensive regulatory information for “Deymed” 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 6946b0365271473b6f660a1398fed0e2 and manufactured by Deymed Diagnostic s.r.o.. The authorized representative in Taiwan is Onemed Co., Ltd..
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