Taiwan FDA registration 2f638fa2a3679ed7de4d7dba9683dbe8
Campanile lumbar disc fusion
TW: 康鉑腰椎椎間盤融合器
Taiwan·Risk Class 2·Guanya Biotechnology Co., Ltd. new store factory·Registered Dec 18, 2012 – Dec 18, 2027ActiveRegistration details
- Analysis ID
- 2f638fa2a3679ed7de4d7dba9683dbe8
Company information
- Manufacturer
- Guanya Biotechnology Co., Ltd. new store factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- A-SPINE Asia Co., Ltd.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3080 椎體間融合裝置
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 18, 2012
- Expiry Date
- Dec 18, 2027
About this record
Access comprehensive regulatory information for Campanile lumbar disc fusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f638fa2a3679ed7de4d7dba9683dbe8 and manufactured by Guanya Biotechnology Co., Ltd. new store factory. The authorized representative in Taiwan is A-SPINE Asia Co., Ltd..
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