Taiwan FDA registration c17e8e2d8cee989de931633bf7385e40

ReBorn Essence Cortical Bone Screw Fixation System

TW: 瑞寶億皮質骨螺釘固定系統
Taiwan flagTaiwan·Risk Class 2·MD·BAUI BIOTECH CO., LTD.·Registered Oct 29, 2018 – Oct 29, 2028Active
Registration details
Analysis ID
c17e8e2d8cee989de931633bf7385e40
License Form
Ministry of Health Medical Device Manufacturing No. 006195
Company information
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)
N3070 Pedicle screw system
Import Information
Produced in Taiwan, China
Dates and status
Registration Date
Oct 29, 2018
Expiry Date
Oct 29, 2028
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About this record

Access comprehensive regulatory information for ReBorn Essence Cortical Bone Screw Fixation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c17e8e2d8cee989de931633bf7385e40 and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BAUI BIOTECH CO., LTD., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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