Taiwan FDA registration 9c36509a8a90bab4ad0b9acef422aded
"Bone Foti" injectable bone filler
TW: “骨福提”注射式骨填充物
Registration details
- Analysis ID
- 9c36509a8a90bab4ad0b9acef422aded
- Customs Code
- DHA00602046006
Company information
- Manufacturer
- GRAFTYS
- Manufacturer Country
- France
- Authorized Representative
- Zhaofeng Biotechnology Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- Dec 03, 2009
- Expiry Date
- Dec 03, 2014
- Cancellation Date
- Jul 31, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Bone Foti" injectable bone filler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9c36509a8a90bab4ad0b9acef422aded and manufactured by GRAFTYS. The authorized representative in Taiwan is Zhaofeng Biotechnology 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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