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“Acandis” Acclino flex plus Stent - Taiwan Registration f6b99b630f3ca0ef268e6796b27501b7

Access comprehensive regulatory information for “Acandis” Acclino flex plus Stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number f6b99b630f3ca0ef268e6796b27501b7 and manufactured by Acandis GmbH. The authorized representative in Taiwan is DR SHAO MD REGULATORY CONSULTANTS CO., LTD..

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f6b99b630f3ca0ef268e6796b27501b7
Registration Details
Taiwan FDA Registration: f6b99b630f3ca0ef268e6796b27501b7
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Device Details

“Acandis” Acclino flex plus Stent
TW: “艾康蒂”艾奇諾支架
Risk Class 3
MD

Registration Details

f6b99b630f3ca0ef268e6796b27501b7

Ministry of Health Medical Device Import No. 032757

DHA05603275702

Company Information

Germany

Product Details

For details, it is Chinese approved copy of the imitation order

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Imported from abroad

Dates and Status

Aug 12, 2019

Aug 12, 2024