Pure Global

ReBorn Essence Y-Motion Connection Rod - Taiwan Registration 189ac1ebaa26d9523773e180e1f0bc71

Access comprehensive regulatory information for ReBorn Essence Y-Motion Connection Rod in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 189ac1ebaa26d9523773e180e1f0bc71 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. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
189ac1ebaa26d9523773e180e1f0bc71
Registration Details
Taiwan FDA Registration: 189ac1ebaa26d9523773e180e1f0bc71
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

ReBorn Essence Y-Motion Connection Rod
TW: ็‘žๅฏถๅ„„ๅจ่Žซๆ—‹้€ฃ็ตๆกฟ
Risk Class 2
MD

Registration Details

189ac1ebaa26d9523773e180e1f0bc71

Ministry of Health Medical Device Manufacturing No. 006910

Company Information

Taiwan, Province of China

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedic devices

N3050 Spine correction fixation between the peduncle plates

Produced in Taiwan, China

Dates and Status

Jul 16, 2020

Sep 20, 2025