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“Arthesys” Pegase Aspiration Catheter - Taiwan Registration 38e12468e6a181ce41f263ba1a1ddf02

Access comprehensive regulatory information for “Arthesys” Pegase 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 38e12468e6a181ce41f263ba1a1ddf02 and manufactured by Arthesys. The authorized representative in Taiwan is HWA YI MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARTHESYS, 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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38e12468e6a181ce41f263ba1a1ddf02
Registration Details
Taiwan FDA Registration: 38e12468e6a181ce41f263ba1a1ddf02
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Device Details

“Arthesys” Pegase Aspiration Catheter
TW: “雅瑟斯”培可熙血栓抽吸導管
Risk Class 2
MD

Registration Details

38e12468e6a181ce41f263ba1a1ddf02

Ministry of Health Medical Device Import No. 029781

DHA05602978102

Company Information

France

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular devices

E5150 Thrombectomy catheter

Imported from abroad

Dates and Status

Jun 05, 2017

Jun 05, 2022

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