Taiwan FDA registration b20ac4d0ae5508e4c281b843c8312f63
“MINATO” Low frequency treatment unit
TW: “美力多”低週波治療儀
Taiwan·Risk Class 2·MD·MINATO MEDICAL SCIENCE CO., LTD. Nishiki Facility·Registered Nov 09, 2015 – Nov 09, 2025ExpiredRegistration details
- Analysis ID
- b20ac4d0ae5508e4c281b843c8312f63
- License Form
- Ministry of Health Medical Device Import No. 027937
- Customs Code
- DHA05602793707
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- GIGA MEDICAL INSTRUMENT LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K5890 Transcutaneous electrical nerve stimulator for pain relief
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 09, 2015
- Expiry Date
- Nov 09, 2025
About this record
Access comprehensive regulatory information for “MINATO” Low frequency treatment unit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b20ac4d0ae5508e4c281b843c8312f63 and manufactured by MINATO MEDICAL SCIENCE CO., LTD. Nishiki Facility. The authorized representative in Taiwan is GIGA MEDICAL INSTRUMENT LTD..
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