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Tekmex bone cement mixer (unsterilized) - Taiwan Registration a6b8bbd748d8ed2880291b9c80500d9e

Access comprehensive regulatory information for Tekmex bone cement mixer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a6b8bbd748d8ed2880291b9c80500d9e and manufactured by TEKNIMED SAS. The authorized representative in Taiwan is GREAT UNITED STRONG ENTERPRISE 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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a6b8bbd748d8ed2880291b9c80500d9e
Registration Details
Taiwan FDA Registration: a6b8bbd748d8ed2880291b9c80500d9e
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Device Details

Tekmex bone cement mixer (unsterilized)
TW: "ๆณฐๅ…‹็พŽ"้ชจๆฐดๆณฅๆ”ชๆ‹Œๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

a6b8bbd748d8ed2880291b9c80500d9e

DHA04401304204

Company Information

France

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Clinical Bone Cement Mixer (N.4210)".

N Orthopedics

N.4210 ่‡จๅบŠ็”จ้ชจๆฐดๆณฅๆ”ชๆ‹Œๅ™จ

import

Dates and Status

May 23, 2013

May 23, 2018

Oct 02, 2015

Cancellation Information

Logged out

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