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“Surefire” Guiding Catheters - Taiwan Registration 4478617ba9dbcc44b528d41c354b1ded

Access comprehensive regulatory information for “Surefire” Guiding Catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4478617ba9dbcc44b528d41c354b1ded 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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4478617ba9dbcc44b528d41c354b1ded
Registration Details
Taiwan FDA Registration: 4478617ba9dbcc44b528d41c354b1ded
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Device Details

“Surefire” Guiding Catheters
TW: “旭發” 導引導管
Risk Class 2
MD
Cancelled

Registration Details

4478617ba9dbcc44b528d41c354b1ded

Ministry of Health Medical Device Import No. 027229

DHA05602722906

Company Information

United States

Product Details

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Mar 18, 2015

Mar 18, 2020

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者