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"Stryker" posterior open lumbar brasion system (sterilization) - Taiwan Registration e32539e9aee714bef7954c889bf4458f

Access comprehensive regulatory information for "Stryker" posterior open lumbar brasion system (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e32539e9aee714bef7954c889bf4458f and manufactured by STRYKER SPINE SAS. The authorized representative in Taiwan is STRYKER FAR EAST INC. TAIWAN BRANCH (USA).

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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e32539e9aee714bef7954c889bf4458f
Registration Details
Taiwan FDA Registration: e32539e9aee714bef7954c889bf4458f
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Device Details

"Stryker" posterior open lumbar brasion system (sterilization)
TW: โ€œๅฒ่ณฝๅ…‹โ€ๅพŒ้–‹่…ฐๆคŽ่ญทๆžถ็ณป็ตฑ(ๆป…่Œ)
Risk Class 2

Registration Details

e32539e9aee714bef7954c889bf4458f

DHA00602406102

Company Information

France

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

Oct 17, 2012

Oct 17, 2027