Taiwan FDA registration 1b55501634199e664efd38e62e65d5a1
“VEINOPLUS”NEUROMUSCULAR STIMULATOR
TW: “舒足健”肌肉刺激儀
Taiwan·Risk Class 2·MD·AD REM TECHNOLOGY·Registered Apr 26, 2022 – Apr 26, 2027ActiveRegistration details
- Analysis ID
- 1b55501634199e664efd38e62e65d5a1
- License Form
- Ministry of Health Medical Device Import No. 035416
- Customs Code
- DHA05603541601
Company information
- Manufacturer
- AD REM TECHNOLOGY
- Manufacturer Country
- France
- 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
- Apr 26, 2022
- Expiry Date
- Apr 26, 2027
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 1b55501634199e664efd38e62e65d5a1 and manufactured by AD REM TECHNOLOGY. The authorized representative in Taiwan is WONDERVILLE CO., LTD..
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