Taiwan FDA registration 9be12ebd91b452b74f997cce38a5666b

“QualiMed” EMAX Aspiration Catheter

TW: “克力美”醫脈司抽吸導管
Taiwan flagTaiwan·Risk Class 2·MD·QualiMed Innovative Medizinprodukte GmbH·Registered Apr 21, 2016 – Apr 21, 2021Cancelled
Registration details
Analysis ID
9be12ebd91b452b74f997cce38a5666b
License Form
Ministry of Health Medical Device Import No. 028517
Customs Code
DHA05602851703
Company information
Manufacturer Country
Germany
Authorized Representative
Pioneer Thai Pharmaceutical Co., Ltd
Product details
Product Type (Level 1)
E Cardiovascular devices
Product Type (Level 2)
E5150 Thrombectomy catheter
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 21, 2016
Expiry Date
Apr 21, 2021
Cancellation Date
Jun 03, 2017
Cancellation information
Status
Logged out
Reason
公司歇業
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About this record

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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