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“Stryker” OMEGA PEEK Knotless Anchor System - Taiwan Registration 2b5cf5edfa0fcdc223c5bc0626eb5af4

Access comprehensive regulatory information for “Stryker” OMEGA PEEK Knotless Anchor System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2b5cf5edfa0fcdc223c5bc0626eb5af4 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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2b5cf5edfa0fcdc223c5bc0626eb5af4
Registration Details
Taiwan FDA Registration: 2b5cf5edfa0fcdc223c5bc0626eb5af4
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Device Details

“Stryker” OMEGA PEEK Knotless Anchor System
TW: “史賽克”無結錨釘固定系統
Risk Class 2
MD

Registration Details

2b5cf5edfa0fcdc223c5bc0626eb5af4

Ministry of Health Medical Device Import No. 034016

DHA05603401606

Company Information

United States

Product Details

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

N Orthopedic devices

N3040 Smooth or threaded metal bone fixation

Imported from abroad

Dates and Status

Nov 05, 2020

Nov 05, 2025