"Stryker" lumbar artificial disc - Taiwan Registration a687a6f76bc5c7a7be26ce4ddd311497
Access comprehensive regulatory information for "Stryker" lumbar artificial disc in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a687a6f76bc5c7a7be26ce4ddd311497 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.
Device Details
Product Details
Indicated for the treatment of lumbar discogenic pain associated with degenerative disc disease (DDD). Replacing a single lumbar disc (L1-S1) with degenerative disease allows flexibility in the portion to be treated, improves function, and reduces back pain associated with DDD.
N Orthopedics
N.3060 ๆค้ซ้ไน่ๆค็ฏๆญฃๅบๅฎ็ฉ
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Dates and Status
Sep 17, 2008
Sep 17, 2013
Nov 15, 2016
Cancellation Information
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