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“QualiMed” EMAX Aspiration Catheter - Taiwan Registration de83d682484fb77434a8e4398dd93bde

Access comprehensive regulatory information for “QualiMed” EMAX Aspiration Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number de83d682484fb77434a8e4398dd93bde and manufactured by QualiMed Innovative Medizinprodukte GmbH. The authorized representative in Taiwan is INTERLINK MEDICAL ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including QualiMed Innovative Medizinprodukte GmbH, and 1 recent registrations in the same category. 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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de83d682484fb77434a8e4398dd93bde
Registration Details
Taiwan FDA Registration: de83d682484fb77434a8e4398dd93bde
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Device Details

“QualiMed” EMAX Aspiration Catheter
TW: “克立玫” 抽吸導管
Risk Class 2
MD
Cancelled

Registration Details

de83d682484fb77434a8e4398dd93bde

Ministry of Health Medical Device Import No. 025421

DHA05602542101

Company Information

Product Details

E Cardiovascular devices

E5150 Thrombectomy catheter

Imported from abroad

Dates and Status

Oct 01, 2013

Oct 01, 2018

Jul 15, 2022

Cancellation Information

Logged out

未展延而逾期者

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