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“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.

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814e67a3d066792f0f43068e08a7e32e
Registration Details
Taiwan FDA Registration: 814e67a3d066792f0f43068e08a7e32e
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Device Details

“Surefire” Infusion System
TW: “旭發”輸液系統
Risk Class 2
MD
Cancelled

Registration Details

814e67a3d066792f0f43068e08a7e32e

Ministry of Health Medical Device Import No. 025444

DHA05602544400

Company Information

United States

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