Pure Global

“Stryker” Cascadia AN 3D Interbody System - Taiwan Registration 1ab104e6c18367b09679d58badeee80b

Access comprehensive regulatory information for “Stryker” Cascadia AN 3D Interbody System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1ab104e6c18367b09679d58badeee80b and manufactured by K2M, INC.. 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
1ab104e6c18367b09679d58badeee80b
Registration Details
Taiwan FDA Registration: 1ab104e6c18367b09679d58badeee80b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Stryker” Cascadia AN 3D Interbody System
TW: “史賽克”凱思卡迪亞三維椎體系統
Risk Class 2
MD

Registration Details

1ab104e6c18367b09679d58badeee80b

Ministry of Health Medical Device Import No. 035394

DHA05603539404

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3080 Interbody fusion device

Imported from abroad

Dates and Status

Apr 20, 2022

Apr 20, 2027