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“Tutogen” CopiOs Pericardium Membrane - Taiwan Registration fdca7f758e3ba429e98819659956dbe4

Access comprehensive regulatory information for “Tutogen” CopiOs Pericardium Membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fdca7f758e3ba429e98819659956dbe4 and manufactured by Tutogen Medical GmbH. The authorized representative in Taiwan is HOWSHINE ENTERPRISE CO., LTD..

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fdca7f758e3ba429e98819659956dbe4
Registration Details
Taiwan FDA Registration: fdca7f758e3ba429e98819659956dbe4
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Device Details

“Tutogen” CopiOs Pericardium Membrane
TW: “凸透晶”口美合牙科用膠原蛋白膜
Risk Class 2
MD

Registration Details

fdca7f758e3ba429e98819659956dbe4

Ministry of Health Medical Device Import No. 026782

DHA05602678202

Company Information

Germany

Product Details

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

F Dental devices

Imported from abroad

Dates and Status

Nov 11, 2014

Nov 11, 2024