Taiwan FDA registration 19489b1da0d950f32620f40f43f955f3

“Arthesys” Pegase Aspiration Catheter

TW: “亞提斯”蓓格爾血栓抽吸導管
Taiwan flagTaiwan·Risk Class 2·MD·ARTHESYS·Registered Dec 22, 2020 – Dec 22, 2025Expired
Registration details
Analysis ID
19489b1da0d950f32620f40f43f955f3
License Form
Ministry of Health Medical Device Import No. 034228
Customs Code
DHA05603422808
Company information
Manufacturer
ARTHESYS
Manufacturer Country
France
Authorized Representative
CATHERINE CONSULTANTS CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
E Cardiovascular devices
Product Type (Level 2)
E5150 Thrombectomy catheter
Import Information
Imported from abroad
Dates and status
Registration Date
Dec 22, 2020
Expiry Date
Dec 22, 2025
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About this record

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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