Taiwan FDA registration 76bb01d3d4b1e2df910d3d80ffdb3aae
Astek Transcutaneous electrical muscle stimulator for pain relief
TW: 亞星珍珠型肌肉刺激器
Taiwan·Risk Class 2·MD·ASTEK TECHNOLOGY LTD.·Registered Dec 29, 2015 – Dec 29, 2025ExpiredRegistration details
- Analysis ID
- 76bb01d3d4b1e2df910d3d80ffdb3aae
- License Form
- Ministry of Health Medical Device Manufacturing No. 005293
Company information
- Manufacturer
- ASTEK TECHNOLOGY LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ASTEK TECHNOLOGY LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5850 powered muscle stimulator
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 29, 2015
- Expiry Date
- Dec 29, 2025
About this record
Access comprehensive regulatory information for Astek Transcutaneous electrical muscle stimulator for pain relief in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 76bb01d3d4b1e2df910d3d80ffdb3aae and manufactured by ASTEK TECHNOLOGY LTD.. The authorized representative in Taiwan is ASTEK TECHNOLOGY LTD..
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