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ReBorn Essence Lumbar Fixation System - ARCSA Registration 408ca4e21b5e3e51fad89333941fc270

Access comprehensive regulatory information for ReBorn Essence Lumbar Fixation System in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 408ca4e21b5e3e51fad89333941fc270 and manufactured by BAUI BIOTECH CO. LTD.. The device was registered on November 24, 2022.

This page provides complete registration details including product type (Invasive), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.

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ARCSA Official Data
III
408ca4e21b5e3e51fad89333941fc270
ReBorn Essence Lumbar Fixation System
ARCSA ID: 408ca4e21b5e3e51fad89333941fc270
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Device Classification
Risk Class
III
Product Type
Invasive
Brand Name
BAUI
Commercial Name
Screws, for Bones
Registration Information
Analysis ID
408ca4e21b5e3e51fad89333941fc270
Registration Date
November 24, 2022
Expiration Date
November 24, 2027
Product Use

THE REBORN ESSENCE LUMBAR FIXATION SYSTEM IS A SYSTEM INDICATED FOR MULTIPLE TYPES OF SPINAL SURGERIES. THE REBORN ESSENCE LUMBAR FIXATION SYSTEM IS INTENDED TO PROVIDE IMMOBILIZATION AND STABILIZATION OF THE SPINE. THE SYSTEM IMPROVES PATIENT RECOVERY BY PROVIDING IMMEDIATE STABILITY, STABILITY FOR THE SPINE AND EARLY MOBILIZATION FOR THE PATIENT.

Manufacturer
City
NEW TAIPEI CITY
Country
TAIWAN
Address
6F, NO.8 SEC. I, ZHONGXING RD., WUGU DIST
Product Owner
Name
BAUI BIOTECH CO. LTD.
Country
TAIWAN
Authorized Representative
Address
PEDROPABLOCARRASCO E8-06 AND AV. ALMAGRO
Phone
23909080