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
Device Details
Titanium subvertebral fixation system
TW: ้ฆไบ่ๆคๅบๅฎ็ณป็ตฑ
Risk Class 2

