Taiwan FDA registration 82d96426062310b7f31e15e0fe1c90ae
"Yingzhi" pulsed magnetic field stimulator
TW: “英智”脈衝磁場刺激儀
Taiwan·Risk Class 2·SHENZHEN YINGCHI TECHNOLOGY CO., LTD.·Registered Jun 24, 2022 – Jun 24, 2027ActiveRegistration details
- Analysis ID
- 82d96426062310b7f31e15e0fe1c90ae
- Customs Code
- DHA09200137100
Company information
- Manufacturer
- SHENZHEN YINGCHI TECHNOLOGY CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- JINGS 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)
- K.5805 重複式經顱磁刺激(rTMS)治療系統
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Jun 24, 2022
- Expiry Date
- Jun 24, 2027
About this record
Access comprehensive regulatory information for "Yingzhi" pulsed magnetic field stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 82d96426062310b7f31e15e0fe1c90ae and manufactured by SHENZHEN YINGCHI TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is JINGS INSTRUMENT CO., LTD..
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