Pure Global

“Wiltrom” Bicera Dental Bone Graft - Taiwan Registration 3f47475d5613fe2aa72d16a61485b7e7

Access comprehensive regulatory information for “Wiltrom” Bicera Dental Bone Graft in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3f47475d5613fe2aa72d16a61485b7e7 and manufactured by Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory. The authorized representative in Taiwan is WILTROM 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
3f47475d5613fe2aa72d16a61485b7e7
Registration Details
Taiwan FDA Registration: 3f47475d5613fe2aa72d16a61485b7e7
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Wiltrom” Bicera Dental Bone Graft
TW: “台微醫”喜瑞骨牙科人工骨替代物
Risk Class 2
MD

Registration Details

3f47475d5613fe2aa72d16a61485b7e7

Ministry of Health Medical Device Manufacturing No. 004523

Company Information

Product Details

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

F Dental devices

F3930 Tricalcium phosphate for alveolar bone restoration

Produced in Taiwan, China

Dates and Status

May 23, 2014

May 23, 2024