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“Teknimed” Cementek LV Synthetic Bone Substitute - Taiwan Registration 26bf793f1c511917a23c8ebe05acacff

Access comprehensive regulatory information for “Teknimed” Cementek LV Synthetic Bone Substitute in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 26bf793f1c511917a23c8ebe05acacff and manufactured by TEKNIMED SAS. The authorized representative in Taiwan is GREAT UNITED STRONG ENTERPRISE CO., LTD..

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26bf793f1c511917a23c8ebe05acacff
Registration Details
Taiwan FDA Registration: 26bf793f1c511917a23c8ebe05acacff
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Device Details

“Teknimed” Cementek LV Synthetic Bone Substitute
TW: “泰克美”希曼骼低黏度人工替代骨
Risk Class 2
MD
Cancelled

Registration Details

26bf793f1c511917a23c8ebe05acacff

Ministry of Health Medical Device Import No. 028172

DHA05602817208

Company Information

France

Product Details

N Orthopedic devices

N3045 Resorbed calcium salt bone cavity filling device

Imported from abroad

Dates and Status

Jan 28, 2016

Jan 28, 2021

Aug 28, 2023

Cancellation Information

Logged out

許可證已逾有效期