Taiwan FDA registration ef4a12625b5ac8d1329c613120b404f4
ReBorn Essence BowLock Interspinous Stabilization Device
TW: “瑞寶億”寶樂脊突間穩定器
Taiwan·Risk Class 3·MD·BAUI BIOTECH CO., LTD.·Registered Jan 11, 2022 – Jan 11, 2028ActiveRegistration details
- Analysis ID
- ef4a12625b5ac8d1329c613120b404f4
- License Form
- Ministry of Health Medical Device Manufacturing No. 006015
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)
- N9999 Other
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jan 11, 2022
- Expiry Date
- Jan 11, 2028
About this record
Access comprehensive regulatory information for ReBorn Essence BowLock Interspinous Stabilization Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number ef4a12625b5ac8d1329c613120b404f4 and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..
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