Taiwan FDA registration b252530f6e741142138ed1e106e1ab89
"Fisomer" multifunctional electrical stimulator
TW: "菲索美"多功能電刺激器
Taiwan·Risk Class 2·PHYSIOMED ELEKTROMEDIZIN AG·Registered Jun 05, 2006 – Jun 05, 2021CancelledRegistration details
- Analysis ID
- b252530f6e741142138ed1e106e1ab89
- Customs Code
- DHA00601662602
Company information
- Manufacturer
- PHYSIOMED ELEKTROMEDIZIN AG
- Manufacturer Country
- Germany
- 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 Neuroscience
- Import Information
- import
Dates and status
- Registration Date
- Jun 05, 2006
- Expiry Date
- Jun 05, 2021
- Cancellation Date
- Aug 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Fisomer" multifunctional electrical stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b252530f6e741142138ed1e106e1ab89 and manufactured by PHYSIOMED ELEKTROMEDIZIN AG. The authorized representative in Taiwan is GIGA MEDICAL INSTRUMENT LTD..
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