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ReBorn Essence Comet Lumbar Interbody Fusion Cage - Taiwan Registration 5751e15021f2cc371f763c46c7b37029

Access comprehensive regulatory information for ReBorn Essence Comet Lumbar Interbody Fusion Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5751e15021f2cc371f763c46c7b37029 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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5751e15021f2cc371f763c46c7b37029
Registration Details
Taiwan FDA Registration: 5751e15021f2cc371f763c46c7b37029
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Device Details

ReBorn Essence Comet Lumbar Interbody Fusion Cage
TW: โ€œ็‘žๅฏถๅ„„โ€ๆŸฏ็พŽ็‰น่…ฐๆคŽๆคŽ้–“่žๅˆๅ™จ
Risk Class 2
MD

Registration Details

5751e15021f2cc371f763c46c7b37029

Ministry of Health Medical Device Manufacturing No. 005465

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

Nov 03, 2016

Nov 03, 2026