Pure Global

“Stryker” G-Lok Suspension Fixation Device - Taiwan Registration 8f1d6bb4a10d8b333e04ace068a8e1cb

Access comprehensive regulatory information for “Stryker” G-Lok Suspension Fixation Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8f1d6bb4a10d8b333e04ace068a8e1cb and manufactured by T.A.G. MEDICAL PRODUCTS CORPORATION LTD.. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
8f1d6bb4a10d8b333e04ace068a8e1cb
Registration Details
Taiwan FDA Registration: 8f1d6bb4a10d8b333e04ace068a8e1cb
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Stryker” G-Lok Suspension Fixation Device
TW: “史賽克”懸吊固定裝置
Risk Class 2
MD

Registration Details

8f1d6bb4a10d8b333e04ace068a8e1cb

Ministry of Health Medical Device Import No. 033846

DHA05603384603

Company Information

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

Aug 27, 2020

Aug 27, 2025