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“TEKNIMED” COHESION BONE CEMENT - Taiwan Registration e910339ac9c08783114d699b8c252463

Access comprehensive regulatory information for “TEKNIMED” COHESION BONE CEMENT in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e910339ac9c08783114d699b8c252463 and manufactured by Teknimed SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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e910339ac9c08783114d699b8c252463
Registration Details
Taiwan FDA Registration: e910339ac9c08783114d699b8c252463
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Device Details

“TEKNIMED” COHESION BONE CEMENT
TW: “泰克美”克西鈞脊固骨水泥
Risk Class 2
MD
Cancelled

Registration Details

e910339ac9c08783114d699b8c252463

Ministry of Health Medical Device Import No. 025611

DHA05602561106

Company Information

France

Product Details

N Orthopedic devices

N3027 PMMA bone cement

Imported from abroad

Dates and Status

Nov 26, 2013

Nov 26, 2023

Aug 28, 2023

Cancellation Information

Logged out

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