Taiwan FDA registration d391378cd3a9d9e7c559931e56b94713
Aiha Tsukasa Intervertebral Fusion
TW: 愛派司椎間融合器
Taiwan·Risk Class 2·A PLUS BIOTECHNOLOGY CO., LTD.·Registered Jul 05, 2018 – Jul 05, 2028ActiveRegistration details
- Analysis ID
- d391378cd3a9d9e7c559931e56b94713
Company information
- Manufacturer
- A PLUS BIOTECHNOLOGY CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- A PLUS BIOTECHNOLOGY 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
- Jul 05, 2018
- Expiry Date
- Jul 05, 2028
About this record
Access comprehensive regulatory information for Aiha Tsukasa Intervertebral Fusion in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d391378cd3a9d9e7c559931e56b94713 and manufactured by A PLUS BIOTECHNOLOGY CO., LTD.. The authorized representative in Taiwan is A PLUS BIOTECHNOLOGY CO., LTD..
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