Taiwan FDA registration 96c1701f71deb375e3e693d6174943c1
"Nihon Medix" Powered Flotation Therapy Bed (Non-Sterile)
TW: "日本醫療"動力式氣流漂浮治療床(未滅菌)
Taiwan·Risk Class 1·MD·NIHON MEDIX CO., LTD. KASHIWA FACTORY·Registered Jan 19, 2015 – Jan 19, 2020CancelledRegistration details
- Analysis ID
- 96c1701f71deb375e3e693d6174943c1
- License Form
- Ministry of Health Medical Device Import No. 014860
- Customs Code
- DHA09401486000
Company information
- Manufacturer
- NIHON MEDIX CO., LTD. KASHIWA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- CROWNMED ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5170 powered airflow floating treatment bed
- Import Information
- Imported from abroad; GMP
Dates and status
- Registration Date
- Jan 19, 2015
- Expiry Date
- Jan 19, 2020
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Nihon Medix" Powered Flotation Therapy Bed (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 96c1701f71deb375e3e693d6174943c1 and manufactured by NIHON MEDIX CO., LTD. KASHIWA FACTORY. The authorized representative in Taiwan is CROWNMED ENTERPRISE CO., LTD..
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