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“phenox” pRESET Thrombectomy Device - Taiwan Registration be2c5f004376b20be46adeb96bf1bb48

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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be2c5f004376b20be46adeb96bf1bb48
Registration Details
Taiwan FDA Registration: be2c5f004376b20be46adeb96bf1bb48
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Device Details

“phenox” pRESET Thrombectomy Device
TW: “菲諾斯”清零血栓切除裝置
Risk Class 2
MD

Registration Details

be2c5f004376b20be46adeb96bf1bb48

Ministry of Health Medical Device Import No. 036011

DHA05603601106

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

K Neuroscience

K5600 Neurovascular mechanical clot removal device for the treatment of acute ischemic stroke

Imported from abroad

Dates and Status

Oct 27, 2022

Oct 27, 2027