Taiwan FDA registration f4770229a0e4ec698b88942239f8ab76
“phenox” Flow Modulation Device
TW: “菲諾斯”流向調變裝置
Taiwan·Risk Class 3·MD·phenox GmbH·Registered Apr 14, 2023 – Apr 14, 2028ActiveRegistration details
- Analysis ID
- f4770229a0e4ec698b88942239f8ab76
- License Form
- Ministry of Health Medical Device Import No. 036473
- Customs Code
- DHA05603647305
Company information
- Manufacturer
- phenox GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- Yuantech International Co, Ltd.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K5950 Artificial embolization device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 14, 2023
- Expiry Date
- Apr 14, 2028
About this record
Access comprehensive regulatory information for “phenox” Flow Modulation Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f4770229a0e4ec698b88942239f8ab76 and manufactured by phenox GmbH. The authorized representative in Taiwan is Yuantech International Co, Ltd..
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