Taiwan FDA registration 4178507b8f83e6c8626b866b06166033
“Remed” UI Cube Electromagnetic Stimulator
TW: “樂美” 優酷磁波刺激器
Taiwan·Risk Class 2·MD·REMED Co., Ltd.·Registered May 24, 2023 – May 24, 2028ActiveRegistration details
- Analysis ID
- 4178507b8f83e6c8626b866b06166033
- License Form
- Ministry of Health Medical Device Import No. 036520
- Customs Code
- DHA05603652001
Company information
- Manufacturer
- REMED Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- DERMACARE BIOMED INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H5320 Non-implantable electronic urination homemade device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 24, 2023
- Expiry Date
- May 24, 2028
About this record
Access comprehensive regulatory information for “Remed” UI Cube Electromagnetic Stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4178507b8f83e6c8626b866b06166033 and manufactured by REMED Co., Ltd.. The authorized representative in Taiwan is DERMACARE BIOMED INC..
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