Taiwan FDA registration 967be331f3ebbff26461cbf73578ba38
ReBorn Essence LIF-PISCES Vertebral Spacer
TW: “瑞寶億”帕西斯椎體支柱塊
Taiwan·Risk Class 2·MD·BAUI BIOTECH CO., LTD.·Registered Dec 17, 2018 – Dec 17, 2028ActiveRegistration details
- Analysis ID
- 967be331f3ebbff26461cbf73578ba38
- License Form
- Ministry of Health Medical Device Manufacturing No. 006309
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
- Dec 17, 2018
- Expiry Date
- Dec 17, 2028
About this record
Access comprehensive regulatory information for ReBorn Essence LIF-PISCES Vertebral Spacer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 967be331f3ebbff26461cbf73578ba38 and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..
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