Taiwan FDA registration 38e12468e6a181ce41f263ba1a1ddf02

“Arthesys” Pegase Aspiration Catheter

TW: “雅瑟斯”培可熙血栓抽吸導管
Taiwan flagTaiwan·Risk Class 2·MD·Arthesys·Registered Jun 05, 2017 – Jun 05, 2022Expired
Registration details
Analysis ID
38e12468e6a181ce41f263ba1a1ddf02
License Form
Ministry of Health Medical Device Import No. 029781
Customs Code
DHA05602978102
Company information
Manufacturer
Arthesys
Manufacturer Country
France
Authorized Representative
HWA YI MEDICAL 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
Jun 05, 2017
Expiry Date
Jun 05, 2022
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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 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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