Taiwan FDA registration 3f47475d5613fe2aa72d16a61485b7e7
“Wiltrom” Bicera Dental Bone Graft
TW: “台微醫”喜瑞骨牙科人工骨替代物
Taiwan·Risk Class 2·MD·Taiwan MicroPort Medical Equipment Co., Ltd. Zhubei Factory·Registered May 23, 2014 – May 23, 2024ExpiredRegistration details
- Analysis ID
- 3f47475d5613fe2aa72d16a61485b7e7
- License Form
- Ministry of Health Medical Device Manufacturing No. 004523
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WILTROM CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3930 Tricalcium phosphate for alveolar bone restoration
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 23, 2014
- Expiry Date
- May 23, 2024
About this record
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..
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