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“Arthesys” Lynx PTA Catheter - Taiwan Registration 4d6fe7bd9726c285cd7f2a2792362a7e

Access comprehensive regulatory information for “Arthesys” Lynx PTA Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4d6fe7bd9726c285cd7f2a2792362a7e and manufactured by ARTHESYS. The authorized representative in Taiwan is HWA YI MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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4d6fe7bd9726c285cd7f2a2792362a7e
Registration Details
Taiwan FDA Registration: 4d6fe7bd9726c285cd7f2a2792362a7e
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Device Details

“Arthesys” Lynx PTA Catheter
TW: “雅瑟斯”林可斯周邊血管氣球導管
Risk Class 2
MD

Registration Details

4d6fe7bd9726c285cd7f2a2792362a7e

Ministry of Health Medical Device Import No. 030402

DHA05603040204

Company Information

France

Product Details

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

E Cardiovascular devices

E1250 Percutaneous catheter

Imported from abroad

Dates and Status

Oct 26, 2017

Oct 26, 2022