Taiwan FDA registration 93401918d0e5afb8a427a7979688f845
“Deymed” Magnetic Stimulator
TW: “萬美德”磁波刺激器
Taiwan·Risk Class 2·MD·Deymed Diagnostic s.r.o.·Registered Jun 20, 2023 – Jun 20, 2028ActiveRegistration details
- Analysis ID
- 93401918d0e5afb8a427a7979688f845
- License Form
- Ministry of Health Medical Device Import No. 036547
- Customs Code
- DHA05603654708
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)
- K1870 Evoked reactive electrical stimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 20, 2023
- Expiry Date
- Jun 20, 2028
About this record
Access comprehensive regulatory information for “Deymed” Magnetic Stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 93401918d0e5afb8a427a7979688f845 and manufactured by Deymed Diagnostic s.r.o.. The authorized representative in Taiwan is Onemed Co., Ltd..
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