“Stryker” PEEK IntraLine Anchor - Taiwan Registration 14d87cbbba890a7bfe7ae619903507c4

Access comprehensive regulatory information for “Stryker” PEEK IntraLine Anchor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 14d87cbbba890a7bfe7ae619903507c4 and manufactured by STRYKER ENDOSCOPY. 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.