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ReBorn Essence Cortical Bone Screw Fixation System (Sterile) - Taiwan Registration 97b335dfd57cd329748bf6fb73a20157

Access comprehensive regulatory information for ReBorn Essence Cortical Bone Screw Fixation System (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 97b335dfd57cd329748bf6fb73a20157 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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97b335dfd57cd329748bf6fb73a20157
Registration Details
Taiwan FDA Registration: 97b335dfd57cd329748bf6fb73a20157
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Device Details

ReBorn Essence Cortical Bone Screw Fixation System (Sterile)
TW: ็‘žๅฏถๅ„„็šฎ่ณช้ชจ่žบ้‡˜ๅ›บๅฎš็ณป็ตฑ(ๆป…่Œ)
Risk Class 2
MD

Registration Details

97b335dfd57cd329748bf6fb73a20157

Ministry of Health Medical Device Manufacturing No. 006933

Company Information

Taiwan, Province of China

Product Details

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

N Orthopedic devices

N3070 Pedicle screw system

Produced in Taiwan, China

Dates and Status

Nov 20, 2020

Nov 20, 2025