Taiwan FDA registration 97b335dfd57cd329748bf6fb73a20157
ReBorn Essence Cortical Bone Screw Fixation System (Sterile)
TW: 瑞寶億皮質骨螺釘固定系統(滅菌)
Taiwan·Risk Class 2·MD·BAUI BIOTECH CO., LTD.·Registered Nov 20, 2020 – Nov 20, 2025ExpiredRegistration details
- Analysis ID
- 97b335dfd57cd329748bf6fb73a20157
- License Form
- Ministry of Health Medical Device Manufacturing No. 006933
Company information
- Manufacturer
- BAUI BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BAUI BIOTECH CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3070 Pedicle screw system
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Nov 20, 2020
- Expiry Date
- Nov 20, 2025
About this record
Access comprehensive regulatory information for ReBorn Essence Cortical Bone Screw Fixation System (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 97b335dfd57cd329748bf6fb73a20157 and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..
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