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“Straumann” XenoGraft - Taiwan Registration 17c7285530ce5f3a32e94efdc14407b3

Access comprehensive regulatory information for “Straumann” XenoGraft in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17c7285530ce5f3a32e94efdc14407b3 and manufactured by NIBEC Co., Ltd. The authorized representative in Taiwan is Straumann Group (Taiwan) 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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17c7285530ce5f3a32e94efdc14407b3
Registration Details
Taiwan FDA Registration: 17c7285530ce5f3a32e94efdc14407b3
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Device Details

“Straumann” XenoGraft
TW: “士卓曼”塞若骨補骨用骨粉
Risk Class 2
MD

Registration Details

17c7285530ce5f3a32e94efdc14407b3

Ministry of Health Medical Device Import No. 034300

DHA05603430003

Company Information

Korea, Republic of

Product Details

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

F Dental devices

F3930 Alveolar Restoration Materials

Imported from abroad

Dates and Status

Mar 04, 2021

Nov 11, 2025