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"Tekme" He-Man artificial replacement bone - Taiwan Registration bb4705fd7256e5a7758fd17d536d7634

Access comprehensive regulatory information for "Tekme" He-Man artificial replacement bone in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bb4705fd7256e5a7758fd17d536d7634 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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bb4705fd7256e5a7758fd17d536d7634
Registration Details
Taiwan FDA Registration: bb4705fd7256e5a7758fd17d536d7634
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Device Details

"Tekme" He-Man artificial replacement bone
TW: โ€œๆณฐๅ…‹็พŽโ€ ๅธŒๆ›ผ้ชผไบบๅทฅๆ›ฟไปฃ้ชจ
Risk Class 2
Cancelled

Registration Details

bb4705fd7256e5a7758fd17d536d7634

DHA00602160600

Company Information

France

Product Details

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

N Orthopedics

N.3045 Absorbable Calcium Salt Bone Cavity Filling Device

import

Dates and Status

Oct 28, 2010

Oct 28, 2015

Aug 14, 2018

Cancellation Information

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