Taiwan FDA registration 631c52be6765b423df69157988707d83
"Astek" Portable IF Stimulator
TW: "亞星"攜帶式中頻電療器
Taiwan·Risk Class 2·MD·ASTEK TECHNOLOGY LTD.·Registered Jan 26, 2016 – Jan 26, 2026ExpiredRegistration details
- Analysis ID
- 631c52be6765b423df69157988707d83
- License Form
- Ministry of Health Medical Device Manufacturing No. 005306
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
- Jan 26, 2016
- Expiry Date
- Jan 26, 2026
About this record
Access comprehensive regulatory information for "Astek" Portable IF Stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 631c52be6765b423df69157988707d83 and manufactured by ASTEK TECHNOLOGY LTD.. The authorized representative in Taiwan is ASTEK TECHNOLOGY LTD..
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