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“XiVE” S Plus Implant System - Taiwan Registration aaa8782324ec6ed287a5ae173317aa16

Access comprehensive regulatory information for “XiVE” S Plus Implant System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number aaa8782324ec6ed287a5ae173317aa16 and manufactured by DENTSPLY IMPLANTS MANUFACTURING GMBH. The authorized representative in Taiwan is DENTSPLY SIRONA INC., TAIWAN BRANCH (U.S.A.).

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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aaa8782324ec6ed287a5ae173317aa16
Registration Details
Taiwan FDA Registration: aaa8782324ec6ed287a5ae173317aa16
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Device Details

“XiVE” S Plus Implant System
TW: “賽芙”牙科植體。
Risk Class 3
MD

Registration Details

aaa8782324ec6ed287a5ae173317aa16

Department of Health Medical Device Import No. 021171

DHA00602117104

Company Information

Product Details

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

F Dental devices

F3640 Bone explants

Imported from abroad

Dates and Status

Jun 29, 2010

Jun 29, 2025