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“phenox” Flow Modulation Device - Taiwan Registration f4770229a0e4ec698b88942239f8ab76

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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f4770229a0e4ec698b88942239f8ab76
Registration Details
Taiwan FDA Registration: f4770229a0e4ec698b88942239f8ab76
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Device Details

“phenox” Flow Modulation Device
TW: “菲諾斯”流向調變裝置
Risk Class 3
MD

Registration Details

f4770229a0e4ec698b88942239f8ab76

Ministry of Health Medical Device Import No. 036473

DHA05603647305

Company Information

Germany

Product Details

Details are as detailed as approved Chinese instructions

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Dates and Status

Apr 14, 2023

Apr 14, 2028