Pure Global

"Stryker" plastic ultrafine catheter - Taiwan Registration 696628de5cc012ded74c16f9f3895148

Access comprehensive regulatory information for "Stryker" plastic ultrafine catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 696628de5cc012ded74c16f9f3895148 and manufactured by Stryker Neurovascular. 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
696628de5cc012ded74c16f9f3895148
Registration Details
Taiwan FDA Registration: 696628de5cc012ded74c16f9f3895148
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Stryker" plastic ultrafine catheter
TW: "ๅฒ่ณฝๅ…‹" ๅก‘ๅž‹่ถ…ๅพฎ็ดฐๅฐŽ็ฎก
Risk Class 2

Registration Details

696628de5cc012ded74c16f9f3895148

DHA00601369006

Company Information

Ireland

Product Details

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

E Cardiovascular Medicine Science

import

Dates and Status

Nov 29, 2005

Nov 29, 2025