Taiwan FDA registration be2c5f004376b20be46adeb96bf1bb48
“phenox” pRESET Thrombectomy Device
TW: “菲諾斯”清零血栓切除裝置
Taiwan·Risk Class 2·MD·phenox GmbH·Registered Oct 27, 2022 – Oct 27, 2027ActiveRegistration details
- Analysis ID
- be2c5f004376b20be46adeb96bf1bb48
- License Form
- Ministry of Health Medical Device Import No. 036011
- Customs Code
- DHA05603601106
Company information
- Manufacturer
- phenox GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- YUANTECH MEDICAL INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K5600 Neurovascular mechanical clot removal device for the treatment of acute ischemic stroke
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 27, 2022
- Expiry Date
- Oct 27, 2027
About this record
Access comprehensive regulatory information for “phenox” pRESET Thrombectomy Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number be2c5f004376b20be46adeb96bf1bb48 and manufactured by phenox GmbH. The authorized representative in Taiwan is YUANTECH MEDICAL INC..
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