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CAPOSS Bone Graft Substitute - Taiwan Registration 5e00159bb4b504e2bd9f33c6eaf7607d

Access comprehensive regulatory information for CAPOSS Bone Graft Substitute in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5e00159bb4b504e2bd9f33c6eaf7607d and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHINEO TECHNOLOGY 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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5e00159bb4b504e2bd9f33c6eaf7607d
Registration Details
Taiwan FDA Registration: 5e00159bb4b504e2bd9f33c6eaf7607d
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Device Details

CAPOSS Bone Graft Substitute
TW: ่‚ฏๆŸไธ–ไบบๅทฅ้ชจๅกซๅ……็‰ฉ
Risk Class 2
MD

Registration Details

5e00159bb4b504e2bd9f33c6eaf7607d

Ministry of Health Medical Device Manufacturing No. 005272

Company Information

Taiwan, Province of China

Product Details

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

N Orthopedic devices

N3045 Resorbed calcium salt bone cavity filling device

Produced in Taiwan, China

Dates and Status

Mar 07, 2016

Mar 07, 2026