Taiwan FDA registration 3a0e9633eded03e8b14b1ddfca1d5172
“ASTEK” INTERMEDIATE FREQUENCY INTERFERENTIAL CURRENT THERAPY
TW: “亞星”中頻向量干擾儀
Taiwan·Risk Class 2·MD·ASTEK TECHNOLOGY LTD.·Registered Mar 05, 2015 – Mar 05, 2025ExpiredRegistration details
- Analysis ID
- 3a0e9633eded03e8b14b1ddfca1d5172
- License Form
- Ministry of Health Medical Device Manufacturing No. 004901
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
- Mar 05, 2015
- Expiry Date
- Mar 05, 2025
About this record
Access comprehensive regulatory information for “ASTEK” INTERMEDIATE FREQUENCY INTERFERENTIAL CURRENT THERAPY in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3a0e9633eded03e8b14b1ddfca1d5172 and manufactured by ASTEK TECHNOLOGY LTD.. The authorized representative in Taiwan is ASTEK TECHNOLOGY LTD..
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