Taiwan FDA registration 17bf38591a3faaa16ea1619ac92cec82
ReBorn Essence Venus Cervical Intervertebral Cage
TW: “瑞寶億”維納斯頸椎椎間融合器
Taiwan·Risk Class 2·MD·BAUI BIOTECH CO., LTD.·Registered Dec 20, 2022 – Dec 20, 2027ActiveRegistration details
- Analysis ID
- 17bf38591a3faaa16ea1619ac92cec82
- License Form
- Ministry of Health Medical Device Manufacturing No. 007719
Company information
- Manufacturer
- BAUI BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BAUI BIOTECH CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N3080 Interbody fusion device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 20, 2022
- Expiry Date
- Dec 20, 2027
About this record
Access comprehensive regulatory information for ReBorn Essence Venus Cervical Intervertebral Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17bf38591a3faaa16ea1619ac92cec82 and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..
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