"Avatek" No-O Intervertebral Fusion Device - Taiwan Registration 50dc5a8154b8366bbfa7af5a89502ad2
Access comprehensive regulatory information for "Avatek" No-O Intervertebral Fusion Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 50dc5a8154b8366bbfa7af5a89502ad2 and manufactured by ALPHATEC SPINE INC.. The authorized representative in Taiwan is K&C MEDICAL 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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50dc5a8154b8366bbfa7af5a89502ad2
Registration Details
Taiwan FDA Registration: 50dc5a8154b8366bbfa7af5a89502ad2
Device Details
"Avatek" No-O Intervertebral Fusion Device
TW: "้ฟไผๆณฐๅ
" ่ซพๆญๆค้่ๅๅจ
Risk Class 2

