Taiwan FDA registration de83d682484fb77434a8e4398dd93bde

“QualiMed” EMAX Aspiration Catheter

TW: “克立玫” 抽吸導管
Taiwan flagTaiwan·Risk Class 2·MD·QualiMed Innovative Medizinprodukte GmbH·Registered Oct 01, 2013 – Oct 01, 2018Cancelled
Registration details
Analysis ID
de83d682484fb77434a8e4398dd93bde
License Form
Ministry of Health Medical Device Import No. 025421
Customs Code
DHA05602542101
Company information
Manufacturer Country
Germany
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
Oct 01, 2013
Expiry Date
Oct 01, 2018
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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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 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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