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“QualiMed” EMAX Aspiration Catheter - Taiwan Registration 9be12ebd91b452b74f997cce38a5666b

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 9be12ebd91b452b74f997cce38a5666b and manufactured by QualiMed Innovative Medizinprodukte GmbH. The authorized representative in Taiwan is Pioneer Thai Pharmaceutical 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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9be12ebd91b452b74f997cce38a5666b
Registration Details
Taiwan FDA Registration: 9be12ebd91b452b74f997cce38a5666b
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Device Details

“QualiMed” EMAX Aspiration Catheter
TW: “克力美”醫脈司抽吸導管
Risk Class 2
MD
Cancelled

Registration Details

9be12ebd91b452b74f997cce38a5666b

Ministry of Health Medical Device Import No. 028517

DHA05602851703

Company Information

Product Details

E Cardiovascular devices

E5150 Thrombectomy catheter

Imported from abroad

Dates and Status

Apr 21, 2016

Apr 21, 2021

Jun 03, 2017

Cancellation Information

Logged out

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