Taiwan FDA registration 383f80946e110c44ef609300b0f71822
Campanile cervical disc fusion
TW: 康鉑頸椎椎間盤融合器
Taiwan·Risk Class 2·Guanya Biotechnology Co., Ltd. new store factory·Registered May 04, 2013 – May 04, 2028ActiveRegistration details
- Analysis ID
- 383f80946e110c44ef609300b0f71822
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
- May 04, 2013
- Expiry Date
- May 04, 2028
About this record
Access comprehensive regulatory information for Campanile cervical 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 383f80946e110c44ef609300b0f71822 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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