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“Stryker” ICONIX SPEED Anchor - Taiwan Registration fd84807980d9f405912e399e88a2ece0

Access comprehensive regulatory information for “Stryker” ICONIX SPEED Anchor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fd84807980d9f405912e399e88a2ece0 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.

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Registration Details
Taiwan FDA Registration: fd84807980d9f405912e399e88a2ece0
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Device Details

“Stryker” ICONIX SPEED Anchor
TW: “史賽克”艾康尼斯固定錨釘
Risk Class 2
MD

Registration Details

fd84807980d9f405912e399e88a2ece0

Ministry of Health Medical Device Import No. 034964

DHA05603496401

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedic devices

N3040 Smooth or threaded metal bone fixation

Imported from abroad

Dates and Status

Oct 03, 2021

Oct 03, 2026