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Titanium subvertebral fixation system - Taiwan Registration cd578e135cb0db1f35ec507d8dcf374a

Access comprehensive regulatory information for Titanium subvertebral fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cd578e135cb0db1f35ec507d8dcf374a and manufactured by JBone Biotechnology Co.,Ltd.. The authorized representative in Taiwan is JBone Biotechnology 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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cd578e135cb0db1f35ec507d8dcf374a
Registration Details
Taiwan FDA Registration: cd578e135cb0db1f35ec507d8dcf374a
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Device Details

Titanium subvertebral fixation system
TW: ้ˆฆไบž่„ŠๆคŽๅ›บๅฎš็ณป็ตฑ
Risk Class 2

Registration Details

cd578e135cb0db1f35ec507d8dcf374a

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N.3070 ๆคŽๅผ“่žบ้‡˜็ณป็ตฑ

Domestic

Dates and Status

Mar 18, 2022

Mar 18, 2027