Taiwan FDA registration b50342455b286ee8eea08726061ae572
“ReBorn Essence”T-Lock Cervical Intervertebral Cage
TW: “瑞寶億”帝洛克頸椎椎間融合器
Taiwan·Risk Class 2·MD·BAUI BIOTECH CO., LTD.·Registered Apr 04, 2019 – Apr 04, 2024ExpiredRegistration details
- Analysis ID
- b50342455b286ee8eea08726061ae572
- License Form
- Ministry of Health Medical Device Manufacturing No. 006335
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)
- N3080 Interbody fusion device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Apr 04, 2019
- Expiry Date
- Apr 04, 2024
About this record
Access comprehensive regulatory information for “ReBorn Essence”T-Lock 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 b50342455b286ee8eea08726061ae572 and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..
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