Taiwan FDA registration 5751e15021f2cc371f763c46c7b37029
ReBorn Essence Comet Lumbar Interbody Fusion Cage
TW: “瑞寶億”柯美特腰椎椎間融合器
Taiwan·Risk Class 2·MD·BAUI BIOTECH CO., LTD.·Registered Nov 03, 2016 – Nov 03, 2026ActiveRegistration details
- Analysis ID
- 5751e15021f2cc371f763c46c7b37029
- License Form
- Ministry of Health Medical Device Manufacturing No. 005465
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
- Nov 03, 2016
- Expiry Date
- Nov 03, 2026
About this record
Access comprehensive regulatory information for ReBorn Essence Comet Lumbar Interbody Fusion Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5751e15021f2cc371f763c46c7b37029 and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..
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