Taiwan FDA registration 3539c838c9a44ff03daa2cf75abd11d9
“Horien” Collagen Bone Graft Substitute
TW: “海昌”膠原蛋白人工骨替代物
Taiwan·Risk Class 2·MD·HORIEN BIOCHEMICAL TECHNOLOGY CO., LTD.·Registered Jul 18, 2016 – Jul 18, 2026ExpiredRegistration details
- Analysis ID
- 3539c838c9a44ff03daa2cf75abd11d9
- License Form
- Ministry of Health Medical Device Manufacturing No. 005382
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)
- N Orthopedic devices
- Product Type (Level 2)
- N3045 Resorbed calcium salt bone cavity filling device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 18, 2016
- Expiry Date
- Jul 18, 2026
About this record
Access comprehensive regulatory information for “Horien” Collagen Bone Graft Substitute in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3539c838c9a44ff03daa2cf75abd11d9 and manufactured by HORIEN BIOCHEMICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HORIEN BIOCHEMICAL TECHNOLOGY CO., LTD..
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