Taiwan FDA registration 189ac1ebaa26d9523773e180e1f0bc71
ReBorn Essence Y-Motion Connection Rod
TW: 瑞寶億威莫旋連結桿
Taiwan·Risk Class 2·MD·BAUI BIOTECH CO., LTD.·Registered Jul 16, 2020 – Sep 20, 2025ExpiredRegistration details
- Analysis ID
- 189ac1ebaa26d9523773e180e1f0bc71
- License Form
- Ministry of Health Medical Device Manufacturing No. 006910
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)
- N3050 Spine correction fixation between the peduncle plates
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 16, 2020
- Expiry Date
- Sep 20, 2025
About this record
Access comprehensive regulatory information for ReBorn Essence Y-Motion Connection Rod in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 189ac1ebaa26d9523773e180e1f0bc71 and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..
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