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“Wiltrom” Osteocera Dental Bone Graft - Taiwan Registration 2de2a3469bc73e1757f49c5a88efa9e7

Access comprehensive regulatory information for “Wiltrom” Osteocera 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 2de2a3469bc73e1757f49c5a88efa9e7 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.

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2de2a3469bc73e1757f49c5a88efa9e7
Registration Details
Taiwan FDA Registration: 2de2a3469bc73e1757f49c5a88efa9e7
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Device Details

“Wiltrom” Osteocera Dental Bone Graft
TW: “台微醫”康骨益牙科人工骨替代物
Risk Class 2
MD

Registration Details

2de2a3469bc73e1757f49c5a88efa9e7

Ministry of Health Medical Device Manufacturing No. 004522

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