“Surefire” Infusion System - Taiwan Registration 814e67a3d066792f0f43068e08a7e32e
Access comprehensive regulatory information for “Surefire” Infusion System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 814e67a3d066792f0f43068e08a7e32e 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.
Device Details
Registration Details
814e67a3d066792f0f43068e08a7e32e
Ministry of Health Medical Device Import No. 025444
DHA05602544400
Product Details
E Cardiovascular devices
E1200 Diagnostic endovascular catheter
Imported from abroad
Dates and Status
Oct 31, 2013
Oct 31, 2018
Aug 05, 2022
Cancellation Information
Logged out
未展延而逾期者

