Taiwan FDA registration 94edf83d9a2f3c8ce94a95943d4547c2
“VEINOPLUS” NEUROMUSCULAR STIMULATOR
TW: “舒足健” 動力式肌肉刺激儀
Taiwan·Risk Class 2·MD·AD REM TECHNOLOGY;;For use only by the Parts System Denda·Registered Nov 19, 2021 – Nov 19, 2026ActiveRegistration details
- Analysis ID
- 94edf83d9a2f3c8ce94a95943d4547c2
- License Form
- Ministry of Health Medical Device Import No. 035033
- Customs Code
- DHA05603503301
Company information
- Manufacturer Country
- France;;United States
- Authorized Representative
- WONDERVILLE CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O5850 powered muscle stimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 19, 2021
- Expiry Date
- Nov 19, 2026
About this record
Access comprehensive regulatory information for “VEINOPLUS” NEUROMUSCULAR STIMULATOR in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 94edf83d9a2f3c8ce94a95943d4547c2 and manufactured by AD REM TECHNOLOGY;;For use only by the Parts System Denda. The authorized representative in Taiwan is WONDERVILLE CO., LTD..
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