Taiwan FDA registration 5bc96fbdd9efd89bc5a0727cb234b260
Ale intervertebral fusion device system
TW: 亞樂椎間融合器系統
Taiwan·Risk Class 2·JBone Biotechnology Co.,Ltd.·Registered Mar 06, 2023 – Mar 06, 2028ActiveRegistration details
- Analysis ID
- 5bc96fbdd9efd89bc5a0727cb234b260
Company information
- Manufacturer
- JBone Biotechnology Co.,Ltd.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JBone Biotechnology Co.,Ltd.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- 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
- Mar 06, 2023
- Expiry Date
- Mar 06, 2028
About this record
Access comprehensive regulatory information for Ale intervertebral fusion device system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5bc96fbdd9efd89bc5a0727cb234b260 and manufactured by JBone Biotechnology Co.,Ltd.. The authorized representative in Taiwan is JBone Biotechnology Co.,Ltd..
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