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“Arthesys” Pegase Aspiration Catheter - Taiwan Registration 19489b1da0d950f32620f40f43f955f3

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 19489b1da0d950f32620f40f43f955f3 and manufactured by ARTHESYS. The authorized representative in Taiwan is CATHERINE CONSULTANTS 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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19489b1da0d950f32620f40f43f955f3
Registration Details
Taiwan FDA Registration: 19489b1da0d950f32620f40f43f955f3
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Device Details

“Arthesys” Pegase Aspiration Catheter
TW: “亞提斯”蓓格爾血栓抽吸導管
Risk Class 2
MD

Registration Details

19489b1da0d950f32620f40f43f955f3

Ministry of Health Medical Device Import No. 034228

DHA05603422808

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

Dec 22, 2020

Dec 22, 2025

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