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"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
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Device Details

"Avatek" No-O Intervertebral Fusion Device
TW: "้˜ฟไผๆณฐๅ…‹" ่ซพๆญๆคŽ้–“่žๅˆๅ™จ
Risk Class 2

Registration Details

50dc5a8154b8366bbfa7af5a89502ad2

DHA00602462302

Company Information

United States

Product Details

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

N Orthopedics

N.3060 ๆคŽ้ซ”้–“ไน‹่„ŠๆคŽ็Ÿฏๆญฃๅ›บๅฎš็‰ฉ

import

Dates and Status

Jan 25, 2013

Jan 25, 2023