Taiwan FDA registration c736be49a2438c4d48b19f654886728f
DenaFit Bone Grafting Material
TW: 帝諾飛特人工骨粉
Taiwan·Risk Class 2·MD·SHINEO TECHNOLOGY CO., LTD.·Registered Mar 08, 2016 – Mar 08, 2026ExpiredRegistration details
- Analysis ID
- c736be49a2438c4d48b19f654886728f
- License Form
- Ministry of Health Medical Device Manufacturing No. 005274
Company information
- Manufacturer
- SHINEO TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SHINEO TECHNOLOGY 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
- Mar 08, 2016
- Expiry Date
- Mar 08, 2026
About this record
Access comprehensive regulatory information for DenaFit Bone Grafting Material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c736be49a2438c4d48b19f654886728f and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHINEO TECHNOLOGY CO., LTD..
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