Pure Global

ReBorn Essence Canis Lumbar Intervertebral Cage - Taiwan Registration 7f5a711d0b59f12dc45e3cad9e318724

Access comprehensive regulatory information for ReBorn Essence Canis Lumbar Intervertebral Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7f5a711d0b59f12dc45e3cad9e318724 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
7f5a711d0b59f12dc45e3cad9e318724
Registration Details
Taiwan FDA Registration: 7f5a711d0b59f12dc45e3cad9e318724
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

ReBorn Essence Canis Lumbar Intervertebral Cage
TW: โ€œ็‘žๅฏถๅ„„โ€่‚ฏๅฐผๆ–ฏ่…ฐๆคŽๆคŽ้–“่žๅˆๅ™จ
Risk Class 2
MD

Registration Details

7f5a711d0b59f12dc45e3cad9e318724

Ministry of Health Medical Device Manufacturing No. 007067

Company Information

Taiwan, Province of China

Product Details

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

N Orthopedic devices

N3080 Interbody fusion device

Produced in Taiwan, China

Dates and Status

Feb 05, 2021

Feb 05, 2026