Taiwan FDA registration 142d88ca98f25184eb62745066a168b1
"Japanese Medical" low frequency therapy device
TW: "日本醫療" 低週波治療儀
Taiwan·Risk Class 2·NIHON MEDIX CO., LTD. KASHIWA FACTORY·Registered Apr 17, 2006 – Apr 17, 2016CancelledRegistration details
- Analysis ID
- 142d88ca98f25184eb62745066a168b1
- Customs Code
- DHA00601429709
Company information
- Manufacturer
- NIHON MEDIX CO., LTD. KASHIWA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- CROWNMED ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Import Information
- import
Dates and status
- Registration Date
- Apr 17, 2006
- Expiry Date
- Apr 17, 2016
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Japanese Medical" low frequency therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 142d88ca98f25184eb62745066a168b1 and manufactured by NIHON MEDIX CO., LTD. KASHIWA FACTORY. The authorized representative in Taiwan is CROWNMED ENTERPRISE CO., LTD..
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