Taiwan FDA registration 256ec21a672989c37e8b2957dccb5c70
“Horien” Collagen Bone Graft Matrix
TW: “海昌”膠原蛋白骨填料
Taiwan·Risk Class 2·MD·HORIEN BIOCHEMICAL TECHNOLOGY CO., LTD.·Registered Sep 01, 2015 – Sep 01, 2025ExpiredRegistration details
- Analysis ID
- 256ec21a672989c37e8b2957dccb5c70
- License Form
- Ministry of Health Medical Device Manufacturing No. 005064
Company information
- Manufacturer
- HORIEN BIOCHEMICAL TECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HORIEN BIOCHEMICAL 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
- Sep 01, 2015
- Expiry Date
- Sep 01, 2025
About this record
Access comprehensive regulatory information for “Horien” Collagen Bone Graft Matrix in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 256ec21a672989c37e8b2957dccb5c70 and manufactured by HORIEN BIOCHEMICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HORIEN BIOCHEMICAL TECHNOLOGY CO., LTD..
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