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“ReBorn Essence”T-Lock Cervical Intervertebral Cage - Taiwan Registration b50342455b286ee8eea08726061ae572

Access comprehensive regulatory information for “ReBorn Essence”T-Lock Cervical 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 b50342455b286ee8eea08726061ae572 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.

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b50342455b286ee8eea08726061ae572
Registration Details
Taiwan FDA Registration: b50342455b286ee8eea08726061ae572
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Device Details

“ReBorn Essence”T-Lock Cervical Intervertebral Cage
TW: “瑞寶億”帝洛克頸椎椎間融合器
Risk Class 2
MD

Registration Details

b50342455b286ee8eea08726061ae572

Ministry of Health Medical Device Manufacturing No. 006335

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

Apr 04, 2019

Apr 04, 2024