Taiwan FDA registration 25905a06a9da5bfa59d57217ec1121ca
“REMED” Electromagnetic Stimulator
TW: “樂密”磁波刺激器
Taiwan·Risk Class 2·MD·Remed Co., Ltd.·Registered Aug 13, 2021 – Aug 13, 2026ActiveRegistration details
- Analysis ID
- 25905a06a9da5bfa59d57217ec1121ca
- License Form
- Ministry of Health Medical Device Import No. 034817
- Customs Code
- DHA05603481701
Company information
- Manufacturer
- Remed Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- BP BIOTECHNOLOGY COMPANY
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- Ø Devices for physical medicine;; K Apparatus for neurology
- Product Type (Level 2)
- O5850 Powered Muscle Stimulator;; K5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 13, 2021
- Expiry Date
- Aug 13, 2026
About this record
Access comprehensive regulatory information for “REMED” 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 25905a06a9da5bfa59d57217ec1121ca and manufactured by Remed Co., Ltd.. The authorized representative in Taiwan is BP BIOTECHNOLOGY COMPANY.
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