Pure Global

“Surefire” Specialty Catheter - Taiwan Registration e4bbb39c232485f682cbbd89f4f194da

Access comprehensive regulatory information for “Surefire” Specialty Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4bbb39c232485f682cbbd89f4f194da and manufactured by Surefire Medical, Inc.. The authorized representative in Taiwan is CEMMA MEDICAL CO., LTD..

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
e4bbb39c232485f682cbbd89f4f194da
Registration Details
Taiwan FDA Registration: e4bbb39c232485f682cbbd89f4f194da
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Surefire” Specialty Catheter
TW: “旭發” 輸液系統專用導管
Risk Class 2
MD
Cancelled

Registration Details

e4bbb39c232485f682cbbd89f4f194da

Ministry of Health Medical Device Import No. 025428

DHA05602542802

Company Information

United States

Product Details

E Cardiovascular devices

E1200 Diagnostic endovascular catheter

Imported from abroad

Dates and Status

Oct 09, 2013

Oct 09, 2018

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者