Taiwan FDA registration 79ef404da4eb25e9590ec63803b2a27c
“funcare” Pulse Therapy Unit
TW: “船井”脈衝儀
Taiwan·Risk Class 2·MD·ASTEK TECHNOLOGY LTD.·Registered Dec 24, 2015 – Dec 24, 2025ExpiredRegistration details
- Analysis ID
- 79ef404da4eb25e9590ec63803b2a27c
- License Form
- Ministry of Health Medical Device Manufacturing No. 005239
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 24, 2015
- Expiry Date
- Dec 24, 2025
About this record
Access comprehensive regulatory information for “funcare” Pulse Therapy Unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 79ef404da4eb25e9590ec63803b2a27c and manufactured by ASTEK TECHNOLOGY LTD.. The authorized representative in Taiwan is ASTEK TECHNOLOGY LTD..
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